Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
NZ748767B2 - Picolinamide compounds with fungicidal activity - Google Patents
[go: Go Back, main page]

NZ748767B2 - Picolinamide compounds with fungicidal activity - Google Patents

Picolinamide compounds with fungicidal activity Download PDF

Info

Publication number
NZ748767B2
NZ748767B2 NZ748767A NZ74876715A NZ748767B2 NZ 748767 B2 NZ748767 B2 NZ 748767B2 NZ 748767 A NZ748767 A NZ 748767A NZ 74876715 A NZ74876715 A NZ 74876715A NZ 748767 B2 NZ748767 B2 NZ 748767B2
Authority
NZ
New Zealand
Prior art keywords
mel
chan
annotation
nmr
mhz
Prior art date
Application number
NZ748767A
Other versions
NZ748767A (en
Inventor
Altamirano Karla Bravo
Zachary Buchan
John Daeuble
Kyle Dekorver
Jessica Herrick
David Jones
Brian Loy
Yu Lu
Kevin Meyer
Jared Rigoli
Original Assignee
Corteva Agriscience Llc
Filing date
Publication date
Application filed by Corteva Agriscience Llc filed Critical Corteva Agriscience Llc
Priority claimed from NZ732641A external-priority patent/NZ732641A/en
Publication of NZ748767A publication Critical patent/NZ748767A/en
Publication of NZ748767B2 publication Critical patent/NZ748767B2/en

Links

Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01G—HORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
    • A01G7/00—Botany in general
    • A01G7/06—Treatment of growing trees or plants, e.g. for preventing decay of wood, for tingeing flowers or wood, for prolonging the life of plants
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
    • A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
    • A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
    • A01P3/00—Fungicides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C229/06—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
    • C07C229/08—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to hydrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C229/20—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated the carbon skeleton being further substituted by halogen atoms or by nitro or nitroso groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C229/22—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated the carbon skeleton being further substituted by oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/46—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/47—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/44—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/52—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/78—Ring systems having three or more relevant rings
    • C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
    • C07D311/82—Xanthenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D313/00—Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
    • C07D333/16—Radicals substituted by singly bound hetero atoms other than halogen by oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

This disclosure relates to picolinamides of Formula I and their use as fungicides. Fungicides are compounds, of natural or synthetic origin, which act to protect and/or cure plants against damage caused by agriculturally relevant fungi. Generally, no single fungicide is useful in all situations. Consequently, research is ongoing to produce fungicides that may have better performance, are easier to use, and cost less.

Description

[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by an PICOLINAMIDE COMPOUNDS WITH FUNGICIDAL TY CROSS REFERENCE TO RELATED APPLICATIONS This application is a divisional of New Zealand patent application no. 732641, which claims the benefit of U.S. Provisional Patent Application Serial Nos. 62/098120 filed December 30, 2014 and 62/098122 filed December 30, 2014, which are expressly incorporated by reference herein.
BACKGROUND & SUMMARY
[0002] ides are compounds, of natural or synthetic origin, which act to protect and/or cure plants against damage caused by agriculturally relevant fungi. Generally, no single fungicide is useful in all ions. Consequently, research is ongoing to produce fungicides that may have better performance, are easier to use, and cost less.
The present disclosure relates to picolinamides and their use as fungicides. The compounds of the t disclosure may offer protection t ascomycetes, basidiomycetes, deuteromycetes and oomycetes.
One embodiment of the present disclosure may include compounds of Formula I: in which: X is hydrogen or C(O)R5; Y is hydrogen, C(O)R5, or Q; wherein: Z is N or CH; R1 is hydrogen or alkyl, each optionally substituted with 0, 1 or multiple R8; R2 is methyl; R1 is chosen from aryl or heteroaryl, each ally substituted with 0, I or multiple R? is chosen from hydrogen, halo, hydroxyl, alkyl or alkoxy; R5 is chosen from alkoxy or oxy, each optionally substituted with 0, 1, or multiple Rx; &, is chosen from hydrogen, alkoxy, or halo, each optionally tuted with 0, 1, or multiple Rx; R7 is chosen from hydrogen,-C(O)R9, or-CH2OC(O)R9; R8 is chosen from hydrogen, alkyl, aryl, acyl, halo, alkenyl, l, alkoxy, cyano or l 0 heterocyclyl, each optionally substituted with 0, 1, or multiple R10; R9 is chosen from alkyl, alkoxy, or aryl, each optionally substituted with 0, 1, or multiple Rx; R10 is chosen from hydrogen, alkyl, aryl, acyl, halo, alkenyl, alkoxy, or heterocyclyl; R11 is chosen fromhydrogen or alkyl, substituted with 0, I, or multiple R8; R12 is chosen from aryl or heteroaryl, each ally substituted with 0, 1 or multiple Another embodiment ofthe present disclosure may include a fungicidal composition for the control or prevention offungal attack comprising the compounds described above and a ogically acceptable carrier material. [00061 Yet another embodiment ofthe present disclosure may inclucle a method for the control or prevention of fungal attack on a plant, the method including the steps of applying a fungicidally effective amount ofone or more ofthe compounds bed above to at least one of the fungus, the plant, and an area adjacent to the plant. [00071 It will be understood by those skilled in the art that the following terms may include generic "R"-groups within their definitions, e.g., "the term alkoxy refers to an-OR substituent". It is also tood that within the definitions for the following terms, these "R" groups are included for illustration purposes and should not be construed as limiting or being limited by substitutions about Formula I.
The term "alkyl" refers to a branched, unbranched, or saturated cyclic carbon chain, ing, but not limited to, methyl, ethyl, propyl, butyl, isopropyl, isobutyl, tertiary butyl, pentyl, hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the like.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan 100091 The term yl" refers to a branched,unbranched or cyclic carbon chain containing one or more double bonds including, but not limited to, ethenyl,propenyl,butenyl, isopropenyl, enyl,cyclobutenyl,cyclopentenyl,cyclohexenyl,and the like.
The term "alkynyl" refers to a branched or unbranched carbon chain containing one or more triple bonds including,but not limited to,propynyl,butynyl,and the like.
The terms "aryl" and "Ar" refer to any ic ring, mono- or bi-cyclic,containing 0 heteroatoms. [0012J The term "heterocyclyl" refers to any aromatic or non-aromatic ring, mono- or bicyclic ,containing one or more heteroatoms. [0013J The term y" refers to an-OR substituent. [00141 The term "acyloxy" refers to an-OC(O)R substituent. [0015J The term "cyano" refers to a-C=N substituent.
The term "hydroxyl" refers to an-OH tuent. 100171 The term "amino" refers to a-N(Rh substituent.
[0018] The term "arylalkoxy" refers to-O(CH2)11Ar where n is an integer selected from the list l,2,3,4,5,or6.
The term "haloalkoxy" refers to an-OR-Xsubstituent, wherein Xis Cl,F, Br, or I,or any combination thereof The term "haloalkyl" refers to an alkyl,which is substituted with Cl, F,I,or Br or any ation thereof [0021J The term "halogen" or "halo" refers to one or more halogen atoms, defined as F, Cl, Br, and I. [0022J The term "nitro" refers to a-N02 substituent. [00231 The term thioalkyl refers to an-SR substituent. [0024J Throughout the sure, reference to the compounds ofFormula I is read as also including all isomers, for example diastereomers, enantiomers, and mixtures thereof. In r embodiment, Formula I is read as also including salts or hydrates thereof. Exemplary salts include, but are not limited to: hydrochloride, hydrobromide, hydroiodide, trifluoroacetate, and trifluoromethane sulfonate.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan 100251 It is also understood by those skilled in the art that additional substitution is allowable, unless otherwise noted, as long as the rules of chemical bonding and strain energy are satisfied and the product still exhibits fungicidal activity Another embodiment ofthe present disclosure is a use ofa nd ofFormula I, for protection of a plant against attack by a phytopathogenic organism or the treatment of a plant infested by a phytopathogenic organism, comprising the application of a compound ofFormula I, or a composition comprising the compound to soil, a plant, a part ofa plant, foliage, and/or roots. [0027J Additionally, another embodiment ofthe present disclosure is a composition useful for protecting a plant against attack by a phytopathogenic organism and/or treatment of a plant infested by a phytopathogenic organism comprising a compound ofFormula I and a phytologically acceptable carrier material.
DETAILED DESCRIPTION 100281 The compounds ofthe present sure may be applied by any of a variety of known techniques, either as the compounds or as formulations comprising the compounds. For example, the compounds may be applied to the roots or e of plants for the control of various fungi, without damaging the commercial value ofthe plants. The als may be applied in the form of any of the generally used formulation types, for example, as solutions, dusts, wettable powders, flowable concentrate, or emulsifiable concentrates. [00291 Preferably, the compounds ofthe present disclosure are applied in the form of a formulation, comprising one or more ofthe nds ofFormula I with a phytologically able carrier. Concentrated formulations may be sed in water, or other s, for application, or formulations may be dust-like or granular, which may then be applied without further treatment The formulations can be prepared according to procedures that are conventional in the agricultural chemical a11.
The present disclosure contemplates all es by which one or more of the compounds may be formulated for ry and use as a fungicide. Typically, formulations are applied as aqueous suspensions or emulsions. Such suspensions or emulsions may be ed from water-soluble, water-suspendible, or emulsifiable ations which are solids, usually known as le powders; or liquids, usually known as emulsifiable concentrates, aqueous suspensions, or suspension concentrates. As will be readily appreciated, any material to which these [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan compounds may be added may be used, provided it yields the desired utility without significant interference with the ty of these compounds as ngal agents. 100311 le powders, which may be ted to form water-dispersible es, comprise an intimate mixture ofone or more of the compounds ofFormula I, an inert r and surfactants The concentration ofthe compound in the wettable powder may be from about l 0 percent to about 90 percent by weight based on the total weight of the wettable powder, more preferably about 25 ,veight t to about 75 weight t In the preparation of wettable powder formulations, the compounds may be compounded with any finely divided solid, such as prophyllite, talc, chalk, gypsum, 's earth, bentonite, attapulgite, starch, casein, gluten, l O montmorillonite clays, diatomaceous earths, purified silicates or the like. In such ions, the finely d carrier and surfactants are typically blended with the compound(s) and milled. [0032J fiable concentrates of the compounds of Formula I may comprise a convenient concentration, such as from about I weight percent to about 50 weight percent of the compound, in a suitable liquid, based on the total weight ofthe concentrate. The compounds may be dissolved in an inert carrier, which is either a water-miscible solvent or a mixture of water-immiscible organic solvents, and emulsifiers. The concentrates may be diluted with water and oil to form spray mixtures in the form of oil-in-water emulsions. Useful organic solvents include aromatics, especially the oiling naphthalenic and olefinic portions of petroleum such as heavy aromatic naphtha. Other organic solvents may also be used, for example, terpenic solvents, including rosin derivatives, aliphatic ketones, such as cyclohexanone, and complex alcohols, such as 2- ethanol. [00331 Emulsifiers which may be advantageously employed herein may be readily determined by those skilled in the art and include various nonionic, anionic, cationic and amphoteric emulsifiers, or a blend oftwo or more emulsifiers. Examples of nonionic emulsifiers useful in ing the emulsifiable concentrates include the polyalkylene glycol ethers and condensation products of alkyl and aryl phenols, aliphatic alcohols, aliphatic amines or fatty acids with ethylene oxide, propylene oxides such as the ethoxylated alkyl phenols and carboxylic esters solubilized with the polyol or polyoxyalkylene. Cationic emulsifiers include nary ammonium compounds and fatty amine salts. Anionic emulsifiers include the oil-soluble salts (e.g., calcium) of alkylaryl sulfonic acids, oil-soluble salts or sulfated polyglycol ethers and appropriate salts ofphosphated polyglycol ether.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan 100341 Representative organic s which may be employed in preparing the emulsifiable concentrates of the compounds of the present disclosure are the aromatic liquids such as xylene, propyl benzene fractions; or mixed naphthalene fractions, mineral oils, substituted aromatic organic liquids such as dioctyl phthalate; kerosene; dialkyl amides of various fatty acids, particularly the dimethyl amides of fatty glycols and glycol derivatives such as then-butyl ether, ethyl ether or methyl ether of diethylene glycol, the methyl ether of ylene glycol, petroleum fractions or hydrocarbons such as mineral oil, aromatic solvents, paraffinic oils, and the like; vegetable oils such as soybean oil, rapeseed oil, olive oil, castor oil, sunflower seed oil, t oil, corn oil, cottonseed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and the like; esters of the l O above vegetable oils; and the like. es of two or more organic liquids may also be employed in the preparation of the emulsifiable concentrate. Organic liquids include xylene, and propyl e fractions, with xylene being most preferred in some cases. Sutiace-active dispersing agents are typically employed in liquid formulations and in an amount of from 0.1 to 20 percent by weight based on the combined weight of the dispersing agent with one or more of the compounds. The formulations can also contain other compatible additives, for example, plant growth tors and other biologically active compounds used in agriculture.
Aqueous suspensions comprise sions of one or more water-insoluble compounds of Formula I, dispersed in an aqueous vehicle at a concentration in the range from about 1 to about 50 weight percent, based on the total weight of the aqueous suspension. Suspensions are prepared by finely grinding one or more of the nds, and vigorously mixing the ground material into a vehicle comprised of water and tants chosen from the same types discussed above. Other components, such as inorganic salts and tic or natural gums, may also be added to increase the density and ity of the aqueous vehicle. [00361 The compounds of a I can also be applied as granular formulations, which are particularly useful for applications to the soil. ar formulations generally contain from about 0.5 to about 10 weight percent, based on the total weight of the granular formulation of the compound(s), dispersed in an inert carrier which consists entirely or in large part of coarsely divided inert material such as attapulgite, bentonite, diatomite, clay or a similar inexpensive substance. Such formulations are usually prepared by dissolving the compounds in a suitable solvent and ng it to a granular carrier which has been preformed to the appropriate particle size, in the range of from about 0.5 to about 3 mm. A suitable solvent is a solvent in which the compound is substantially or [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an completely soluble. Such formulations may also be prepared by making a dough or paste of the carrier and the compound and solvent, and crushing and drying to obtain the desired granular particle.
Dusts containing the compounds of a I may be prepared by intimately mixing one or more of the compounds in powdered form with a suitable dusty agricultural carrier, such as, for example, kaolin clay, ground ic rock, and the like. Dusts can suitably contain from about 1 to about 10 weight t of the compounds, based on the total weight of the dust [0038J The formulations may additionally contain adjuvant surfactants to enhance deposition, wetting, and penetration of the compounds onto the target crop and sm. These adjuvant tants may optionally be employed as a component of the formulation or as a tank mix. The amount of adjuvant surfactant will typically vary from 0.01 to 1.0 percent by volume, based on a spray-volume of water, preferably 0.05 to 0.5 volume percent le adjuvant swfactants include, but are not limited to ethoxylated nonyl phenols, ethoxylated synthetic or l alcohols, salts of the esters or sulfosuccinic acids, ethoxylated organosilicones, ethoxylated fatty amines, blends of surfactants with mineral or ble oils, crop oil concentrate (mineral oil (85%) + emulsifiers ( 15%)); henol ethoxylate; benzylcocoalkyldimethyl quaternary ammonium salt; blend of petroleum hydrocarbon, alkyl esters, organic acid, and anionic surfactant; C9- Cu alkylpolyglycoside; phosphated alcohol ethoxylate; l primary alcohol (C 12 - C 1r,) ethoxylate; di-sec-butylphenol EO-PO block copolymer; polysiloxane-methyl cap; nonylphenol ethoxylate + urea ammonium nitrrate; emulsified methylated seed oil; tridecyl alcohol (synthetic) ethoxylate (8EO); tallow amine ethoxylate (15 EO); PEG(400) dioleate-99. The formulations may also include oil-in-water emulsions such as those sed in US Patent Application Serial No. 11/495,228, the disclosure of which is sly incorporated by nce herein. [00391 The formulations may optionally include ations that contain other pesticidal compounds. Such additional idal compounds may be fungicides, insecticides, herbicides, cides, miticides, arthropodicides, bactericides or combinations thereof that are compatible with the compounds of the present disclosure in the medium selected for application, and not antagonistic to the activity of the present compounds. Accordingly, in such embodiments, the other pesticidal compound is employed as a supplemental toxicant for the same or for a different pesticidal use. The compounds of Formula I and the pesticidal compound in the combination can generally be present in a weight ratio of from 1:100 to100:1.
[Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan 100401 The compounds of the present disclosure may also be ed with other fungicides to form fungicidal mixtures and synergistic mixtures thereof. The fungicidal compounds of the present disclosure are often applied in conjunction with one or more other fungicides to control a wider variety of undesirable diseases. When used in conjunction with other ide(s), the presently claimed compounds may be formulated with the other fungicide(s), ixed with the other fungicide(s) or applied sequentially with the other fungicide(s). Such other fungicides may include 2-(thiocyanatomethylthio)-benzothiazole, 2-phenylphenol, 8-hydroxyquinoline e, ametoctradin, amisulbrom, antimycin, myces quisqualis, azaconazole, azoxystrobin, Bacillus subti!is, Bacillus subti!is strain QST713, benalaxyl, benomyl, benthiavalicarb-isopropyl, indiflupyr, benzylaminobenzene-sulfonate (BABS) salt, bicarbonates, biphenyl, bismerthiazol, anol, bixafen, blasticidin-S, borax, Bordeaux mixture, boscalid, bromuconazole, bupirimate, calcium polysulfide, captafol, captan, carbendazim, carboxin, carpropamid, carvone, chlazafenone, chloroneb, chlorothalonil, chlozolinate, Coniothyrium ns, copper hydroxide, copper octanoate, copper oxychloride, copper sulfate, copper sulfate (tribasic), coumoxystrobin, cuprous oxide, cyazofamid, cyflufenamid, cymoxanil, cyproconazole, cyprodinil, dazomet, debacarb, diammonium ethylenebis-(dithiocarbamate), dichlotluanid, dichlorophen, diclocymet, diclomezine, dichloran, fencarb, difenoconazole, difenzoquat ion, diflumetorim, dimethomorph, dimoxystrobin, nazole, diniconazole-M, dinobuton, dinocap, diphenylamine, dipymetitrone, dithianon, dodemorph, dodemorph acetate, dodine, dodine free base, edifenphos, enestrobin, enestroburin, enoxastrobin, epoxiconazole, ethaboxam, ethoxyquin, etridiazole, famoxadone, fenamidone, fenaminostrobin, fenarimol, fenbuconazole, fenfuram, fenhexamid, fenoxanil, fenpiclonil, fenpropidin, fenpropimorph, azamine, fentin, fentin acetate, fentin hydroxide, , one, fluazinam, fludioxonil, flufenoxystrobin, flumorph, fluopicolide, tluopyram, imide, tluoxastrobin, tluquinconazole, tlusilazole, tlusulfamide, tlutianil, anil, flutriafol, fluxapyroxad, folpet, formaldehyde, fosetyl, fosetyl-aluminium, fuberidazole, furalaxyl, furametpyr, guazatine, guazatine acetates, GY-81, hexachlorobenzene, hexaconazole, hymexazol, imazalil, imazalil sulfate, imibenconazole, iminoctadine, tadine triacetate, iminoctadine tris(albesilate), iodocarb, ipconazole, ipfenpyrazolone, iprobenfos, iprodione, iprovalicarb, isofetamid, isoprothiolane, isopyrazam, nil, kasugamycin, kasugamycin hydrochloride hydrate, kresoxim-methyl, laminarin, mancopper, mancozeb, mandestrobin, mandipropamid, maneb, mefenoxam, mepanipyrim, mepronil, -dinocap, mercuric chloride, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan mercuric oxide, mercurous chloride, metalaxyl, metalaxyl-M, metam, metam-ammonium, metampotassium , metam-sodium, metconazole, methasulfocarb, methyl iodide, methyl isothiocyanate, metiram, metominostrobin, metrafenone, mildiomycin, myclobutanil, nabam, nitrothal-isopropyl, nuarimol, octhilinone, ofurace, oleic acid (fatty acids), orysastrobin, yl, oxathiapiprolin, oxine-copper, oxpoconazole fumarate, oxycarboxin, pefurazoate, penconazole, pencycuron, penflufen, pentachlorophenol, pentachlorophenyl laurate, penthiopyrad, phenylmercury acetate, phosphonic acid, phthalide, picarbutrazox, picoxystrobin, polyoxin B, polyoxins, polyoxorim, potassium bicarbonate, potassium hydroxyquinoline sulfate, azole, prochloraz, procymidone, propamocarb, propamocarb hydrochloride, propiconazole, propineb, proquinazid, prothioconazole, l 0 pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyraziflumid, pyrazophos, pyribencarb, pyributicarb, pyrifenox, pyrimethanil, pyriofenone, pyrisoxazole, pyroquilon, quinoclamine, quinoxyfen, quintozene, Rey11011tria sachalinensis extract, sedaxane, silthiofam, simeconazole, sodium 2-phenylphenoxide, sodium bicarbonate, sodium pentachlorophenoxide, amine, sulfur, SYP-Z048, tar oils, tebuconazole, tebufloquin, tecnazene, tetraconazole, thiabendazole, thifluzamide, anate-methyl, thiram, tiadinil, tolclofos-methyl, carb, luanid, triadimefon, triadimenol, triazoxide, triclopyricarb, tricyclazole, tridemorph, xystrobin, triflumizole, triforine, triticonazole, validamycin, nalate, valiphenal, vinclozolin, zineb, ziram, zoxamide, Candida ila,F11sari11m l)()rllm, Gliodadi11m spp., Phlehiopsis gigan/ea, Streptomyces griseoviridis, Trichoderma spp., (RS)-N-(3,5-dichl oropheny1)(methoxymethy1)- succinimide, 1,2-dichloropropane, 1,3-dichloro-1, 1,3,3-tetrafluoroacetone hydrate, 1-chloro-2,4- dinitronaphthalene, l-chloronitropropane, 2-(2-heptadecylimidazolin-l-yl)ethanol, 2,3- dihydrophenyl-1,4-dithi-ine 1,1,4,4-tetraoxide, 2-methoxyethylmercury acetate, 2- methoxyethylmercury chloride, 2-methoxyethylmercury silicate, hlorophenyl) methylrhodanine, 4-(2-nitropropenyl)phenyl thiocyanateme, ampropylfos, ine, azithiram, barium polysulfide, Bayer 32394, benodanil, benquinox, bentaluron, acril, acrilisobutyl , benzamorf, binapacryl, thylmercury) sulfate, bis(tributyltin) oxide, buthiobate, m calcium copper zinc chromate sulfate, carbamorph, CECA, chlobenthiazone, chloraniformethan, chlorfenazole, chlorquinox, climbazole, copper bis(3-phenylsalicylate), copper zinc chromate, eb, cupric hydrazinium sulfate, cuprobam, cyclafuramid, cypendazole, cyprofuram, decafentin, dichlone, dichlozoline, diclobutrazol, dimethirimol, dinocton, dinosulfon, dinoterbon, dipyrithione, ditalimfos, dodicin, drazoxolon, EBP, ESBP, etaconazole, etem, ethirim, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan nosult? fenapanil, fenitropan, imazole, furcarbanil, furconazole, furconazole-cis, furmecyclox, furophanate, glyodine, griseofulvin, halacrinate, Hercules 3944, hexylthiofos, ICIA0858, isopamphos, isovaledione, mebenil, mecarbinzid, metazoxolon, methfuroxam, methylmercury dicyandiamide, fovax, , mucochloric anhydride, myclozolin, N-3,SS dichlorophenyl-succinimide, trophenylitaconimide, natamycin, N-ethylmercurio toluenesulfonanilide, nickel bis(dimethyldithiocarbamate), OCH, phenylmercury dimethyldithiocarbamate, phenylmercury e, phosdiphen, prothiocarb, prothiocarb hydrochloride, pyracarbolid, nitril, pyroxychlor, pyroxyfur, quinacetol, quinacetol sulfate, quinazamid, quinconazole, rabenzazole, salicylanilide, 9, sultropen, tecoram, thiadifluor, l O thicyofen, thiochlo1fonphim, thiophanate, thioquinox, id, triamiphos, triarimol, triazbutil, trichlamide, urbacid, zarilamid, and any combinations thereof. [0041J Additionally, the compounds bed herein may be combined with other pesticides, including insecticides, nematocides, miticides, arthropodicides, bactericides or combinations thereof that are compatible \vith the compounds of the present disclosure in the medium selected for application, and not antagonistic to the activity of the present compounds to form idal es and istic mixtures thereof The fungicidal compounds ofthe present disclosure may be applied in ction with one or more other pesticides to control a wider variety of undesirable pests. When used in conjunction with other pesticides, the presently claimed compounds may be formulated with the other pesticide(s), tank-mixed with the other pesticide(s) or applied sequentially with the other pesticide(s). Typical insecticides include, but are not limited to: 1,2-dichloropropane, abamectin, acephate, acetamiprid, acethion, acetoprole, acrinathrin, acrylonitrile, afidopyropen, alanycarb, aldicarb, carb, aldrin, allethrin, allosamidin, allyxycarb, alpha-cypermethrin, alpha-ecdysone, alpha-endosulfan, amidithion, aminocarb, amiton, amiton oxalate, amitraz, anabasine, thion, azadirachtin, azamethiphos, azinphos-ethyl, azinphos-methyl, azothoate, barium hexafluorosilicate, in, bendiocarb, benfuracarb, bensultap, beta-cyfluthrin, betacypermethrin , bifenthrin, bioallethrin, anomethrin, biopermethrin, bistrifluron, borax, boric acid, broflanilide, nvinfos, bromocyclen, bromo-DDT, bromophos, bromophos-ethyl, bufencarb, buprofezin, butacarb, butathiofos, butocarboxim, butonate, butoxycarboxim, cadusafos, calcium arsenate, calcium lfide, camphechlor, carbanolate, yl, carbofuran, carbon disulfide, carbon tetrachloride, carbophenothion, carbosulfan, cartap, cartap hydrochloride, chlorantraniliprole, chlorbicyclen, chlordane, chlordecone, chlordimeform, chlordimeform [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan hydrochloride, chlorethoxyfos, chlorfenapyr, chlorfenvinphos, chlortluazuron, chlormephos, chloroform, picrin, chlorphoxim, chlorprazophos, chlorpyrifos, chlorpyrifos-methyl, chlorthiophos, chromafenozide, cinerin I, n II, cinerins, cismethrin, clacyfos, cloethocarb, closantel, clothianidin, copper acetoarsenite, copper arsenate, copper naphthenate, copper , coumaphos, coumithoate, crotamiton, crotoxyphos, cmfomate, cryolite, cyanofenphos, cyanophos, cyanthoate, cyantraniliprole, cyclaniliprole, cyclethrin, cycloprothrin, cytluthrin, cyhalothrin, cypermethrin, cyphenothrin, cyromazine, cythioate, DDT, decarbofuran, deltamethrin, demephion, demephion-O, demephion-S, n, demeton-methyl, demeton-O, demeton-O-methyl, demeton­ S, demeton-S-methyl, demeton-S-methylsulphon, thiuron, dialifos, diatomaceous earth, l O on, dicapthon, dichlofenthion, dichlorvos, dicloromezotiaz, dicresyl, dicrotophos, dicyclanil, dieldrin, ditlubenzuron, dilor, dimefluthrin, dimefox, dimetan, dimethoate, dimethrin, dimethylvinphos, dimetilan, dinex, dinex-diclexine, dinoprop, dinosam, dinotefuran, diofenolan, dioxabenzofos, dioxacarb, dioxathion, disulfoton, dithicrofos, d-limonene, DNOC, DNOC­ ammonium, DNOC-potassium, DNOC-sodium, ctin, ecdysterone, tin, emamectin te, EMPC, hrin, endosulfan, endothion, endrin, EPN, epofenonane, eprinomectin, esdepallethrine, alerate, etaphos, ethiofencarb, ethion, ethiprole, ethoate-methyl, ethoprophos, ethyl formate, ethyl-DDD, ne dibromide, ethylene dichloride, ethylene oxide, etofenprox, os, EXD, famphur, fenamiphos, fenazatlor, fenchlorphos, fenethacarb, fentluthrin, fenitrothion, fenobucarb, fenoxacrim, fenoxycarb, fenpirithrin, fenpropathrin, fensulfothion, fenthion, fenthion-ethyl, fenvalerate, fipronil, tlometoquin, tlonicamid, tlubendiamide, tlucofuron, flucycloxuron, flucythrinate, flufenerim, flufenoxuron, prox, flufiprole, fluhexafon, tlupyradifurone, tluvalinate, fonofos, formetanate, formetanate hloride, formothion, formparanate, formparanate hloride, fosmethilan, fospirate, fosthietan, furathiocarb, furethrin, gamma-cyhalothrin, gamma-HCH, halfenprox, halofenozide, HCH, HEOD, hlor, heptafluthrin, heptenophos, heterophos, hexaflumuron, HHDN, hydramethylnon, hydrogen cyanide, hydroprene, hyquincarb, imidacloprid, imiprothrin, indoxacarb, iodomethane, IPSP, isazofos, isobenzan, isocarbophos, isodrin, isofenphos, isofenphos-methyl, isoprocarb, isoprothiolane, isothioate, isoxathion, ivermectin, jasmolin I, jasmolin II, jodfenphos, juvenile hormone I, juvenile hormone II, juvenile hormone III, kappa-bifenthrin, kappa-tefluthrin, n, kinoprene, lambda- cyhalothrin, lead arsenate, lepimectin, leptophos, lindane, os, lufenuron, lythidathion, malathion, malonoben, mazidox, mecarbam, mecarphon, menazon, mephosfolan, mercurous [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan chloride, mesulfenfos, metaflumizone, methacrifos, methamidophos, methidathion, methiocarb, methocrotophos, methomyl, methoprene, ychlor, methoxyfenozide, methyl e, methyl isothiocyanate, methylchloroform, ene chloride, metofluthrin, metolcarb, metoxadiazone, mevinphos, mexacarbate, milbemectin, milbemycin oxime, mipafox, mirex, molosultap, momfluorothrin, monocrotophos, hypo, monosultap, morphothion, moxidectin, naftalofos, naled, naphthalene, nicotine, nifluridide, nitenpyram, nithiazine, nitrilacarb, novaluron, noviflumuron, omethoate, oxamyl, oxydemeton-methyl, oxydeprofos, oxydisulfoton, paradichlorobenzene , parathion, ion-methyl, penfluron, pentachlorophenol, permethrin, phenkapton, phenothrin, oate, phorate, phosalone, phosfolan, phosmet, phosnichlor, phosphamidon, phosphine, phoxim, phoxim-methyl, pirimetaphos, pirimicarb, pirimiphos-ethyl, pirimiphos-methyl, potassium arsenite, potassium thiocyanate, pp'-DDT, prallethrin, ene I, precocene II, precocene III, primidophos, profenofos, profluralin, promacyl, promecarb, propaphos, propetamphos, propoxur, dathion, ofos, ate, protrifenbute, pyflubumide, pyraclofos, pyrafluprole, pyrazophos, ethrin, pyrethrin I, pyrethrin II, pyrethrins, pyridaben, pyridalyl, pyridaphenthion, pyrifluquinazon, pyrimidifen, pyriminostrobin, tate, pyriprole, oxyfen, quassia, quinalphos, phos-methyl, quinothion, rafoxanide, resmethrin, rotenone, ryania, sabadilla, schradan, selamectin, silafluofen, silica gel, sodium arsenite, sodium de, sodium hexafluorosilicate, sodium thiocyanate, sophamide, spinetoram, spinosad, spiromesifen, spirotetramat, sulcofuron, sulcofuron-sodium, sulfluramid, sulfotep, sulfoxaflor, sulfuryl fluoride, sulprofos, tau-fluvalinate, tazimcarb, TDE, tebufenozide, tebufenpyrad, tebupirimfos, teflubenzuron, hrin, temephos, TEPP, terallethrin, terbufos, tetrachloroethane, tetrachlorvinphos, tetramethrin, tetramethylfluthrin, tetraniliprole, theta-cypermethrin, thiacloprid, thiamethoxam, thicrofos, thiocarboxime, thiocyclam, clam oxalate, thiodicarb, thiofanox, thiometon, thiosultap, thiosultap-disodium, thiosultap-monosodium, thuringiensin, tioxazafen, tolfenpyrad, tralomethrin, transfluthrin, transpermethrin, thene, triazamate, triazophos, trichlorfon, trichlormetaphos-3, trichloronat, trifenofos, triflumezopyrim, triflumuron, trimethacarb, ne, thion, vaniliprole, XMC, xylylcarb, zeta-cypermethrin, zolaprofos, and any combinations thereof.
Additionally, the compounds described herein may be combined with herbicides that are compatible with the compounds of the present disclosure in the medium selected for application, and not nistic to the activity of the present compounds to form pesticidal mixtures and [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan synergistic mixtures thereof The fungicidal compounds of the present disclosure may be applied in conjunction with one or more herbicides to control a wide variety of undesirable plants. When used in conjunction with herbicides, the presently claimed compounds may be formulated with the ide(s), tank-mixed with the ide(s) or applied sequentially with the herbicide(s). Typical herbicides include, but are not limited to 4-CPA, 4-CPB; 4-CPP; 2,4-D; 3,4-DA; 2,4-DB; 3,4-DB; 2,4-DEB; 2,4-DEP; 3,4-DP; 2,3,6-TBA; 2,4,5-T; 2,4,5-TB; acetochlor, acifluorfen, aclonifen, in, alachlor, allidochlor, alloxydim, ally] alcohol, alorac, dione, ametryn, amibuzin, amicarbazone, amidosulfuron, yclopyrachlor, aminopyralid, amiprofos-methyl, amitrole, ammonium ate, anilofos, anisuron, asulam, atraton, atrazine, azafenidin, azimsulfuron, tryne, barban, BCPC, beflubutamid, benazolin, bencarbazone, benfluralin, benfuresate, bensulfuron, bensulide, bentazone, benzadox, benzfendizone, benzipram, benzobicyclon, benzofenap, benzofluor, benzoylprop, benzthiazuron, bicyclopyrone, bifenox, bilanafos, bispyribac, borax, bromacil, onil, bromobutide, bromofenoxim, bromoxynil, brompyrazon, butachlor, butafenacil, butamifos, butenachlor, buthidazole, buthiuron, in, butroxydim, n, butylate, cacodylic acid, cafenstrole, calcium te, m cyanamide, cambendichlor, carbasulam, carbetamicle, carboxazole, chlorprocarb, cait'entrazone, CDEA, CEPC, chlomethoxyfen, chloramben, chloranocryl, zifop, chlorazine, chlorbromuron, chlorbufam, chloreturon, chlorfenac, chlorfenprop, chlorflurazole, chlorflurenol, chloridazon, chlorimuron, chlornitrofen, chloropon, chlorotoluron, chloroxuron, chloroxynil, chlorpropham, chlorsulfuron, chlorthal, hiamid, cinidon-ethyl, cinmethylin, lfuron, cisanilide, clethoclim, cliodinate, clodinafop, clofop, one, clomeprop, cloprop, cloproxydim, alid, cloransulam, CMA, copper sulfate, CPNJF, CPPC, credazine, cresol, cumyluron, cyanatryn, cyanazine, cycloate, cyclopyrimorate, cyclosulfamuron, cycloxydim, cycluron, cyhalofop, cyperquat, cyprazine, cyprazole, cypromid, daimuron, dalapon, dazomet, delachlor, desmedipham, desmetryn, di-allate, dicamba, benil, ralurea, dichlormate, dichlorprop, dichlorprop-P, diclofop, diclosulam, diethamquat, diethatyl, difenopenten, difenoxuron, difenzoquat, enican, diflufenzopyr, dimefuron, dimepiperate, dimethachlor, dimethametryn, dimethenamid, dimethenamid-P, dimexano, dimidazon, dinitramine, dinofenate, dinoprop, dinosam, dinoseb, dinoterb, diphenamid, dipropetryn, diquat, disul, dithiopyr, , DMPA, DNOC, DSMA, EBEP, eglinazine, endothal, epronaz, EPTC, erbon, esprocarb,ethalfluralin, ethametsulfuron, ethidimuron, ethiolate, ethofumesate,ethoxyfen, ethoxysulfuron, etinofen, etnipromid, zanid, EXD, fenasulam, [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan fenoprop, fenoxaprop, fenoxaprop-P, fenmasulfone, notrione, fenteracol, fenthiaprop, fentrazamide, fenuron, ferrous sulfate, op, flamprop-M, flazasulfuron, florasulam, fluazifop, fluazifop-P, fluazolate, flucarbazone, flucetosulfuron, oralin, flufenacet, flufenican, flufenpyr, flumetsulam, flumezin, flumiclorac, xazin, flumipropyn, fluometuron, fluorodifen, fluoroglycofen, fluoromidine, fluoronitrofen, fluothiuron, flupoxam, flupropacil, panate, flupyrsulfuron, fluridone, flurochloridone, fluroxypyr, flurtamone, fluthiacet, fen, foramsulfuron, fosamine, x:yfen, glufosinate, glufosinate-P, glyphosate, halauxifen, halosafen, halosulfuron, haloxydine, haloxyfop, haloxyfop-P, hexachloroacetone, hexaflurate, hexazinone, imazamethabenz, imazamox, imazapic, yr, imazaquin, imazethapyr, ulfuron, indanofan, indaziflam, iodobonil, iodomethane, iodosulfuron, iofensulfuron, ioxynil, ipazine, ipfencarbazone, iprymidam, isocarbamid, , isomethiozin, isonoruron, isopolinate, isopropalin, isoproturon, isouron, isoxaben, isoxachl011ole, isoxaflutole, isoxapyrifop, karbutilate, ketospiradox, lactofen, lenacil, linuron, MAA, MAMA, MCPA, MCPA-thioethyl, MCPB, mecoprop, mecoprop­ P, medinoterb, mefenacet, mefluidide, mesoprazine, mesosulfuron, mesotrione, metam, metamifop, metamitron, metazachlor, metazosulfuron, metflurazon, methabenzthiazuron, methalpropalin, methazole, methiobencarb, methiozolin, methiuron, methometon, methoprotryne, methyl bromide, methyl ocyanate, methyldymron, metobenzuron, metobromuron, chlor, metosulam, ron, metribuzin, metsulfuron, molinate, monalide, monisouron, monochloroacetic acid, monolinuron, monuron, morfamquat, MSMA, naproanilide, napropamide, napropamide-M, naptalam, neburon, nicosulfuron, clofen, nitralin, nitrofen, nitrofluorfen, razon, noruron, OCH, orbencarb, ortho-dichlorobenzene, orthosulfamuron, oryzalin, oxadiargyl, oxadiazon, oxapyrazon, oxasulfuron, oxaziclomefone, oxyfluorfen, parafluron, paraquat, pebulate, pelargonic acid, pendimethalin, penoxsulam, pentachlorophenol, pentanochlor, azone, perfluidone, amid, phenisopham, phenmedipham, phenmedipham-ethyl, phenobenzuron, mercury acetate, picloram, picolinafen, pinoxaden, piperophos, potassium arsenite, potassium azide, potassium e, pretilachlor, primisulfuron, procyazine, prodiamine, profluazol, profluralin, profoxydim, proglinazine, prometon, prometryn, propachlor, propanil, propaquizafop, propazine, propham, propisochlor, propoxycarbazone, propyrisulfuron, propyzamide, prosulfalin, prosulfocarb, prosulfuron, proxan, prynachlor, pydanon, pyraclonil, ufen, pyrasulfotole, pyrazolynate, pyrazosulfuron, pyrazoxyfen, pyribenzoxim, pyributicarb, pyriclor, pyridafol, pyridate, alid, pyriminobac, sulfan, pyrithiobac, pyroxasulfone, pyroxsulam, quinclorac, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an quinmerac, quinoclamine, amid, quizalofop, quizalofop-P, rhodethanil, rimsulfuron, saflufenacil, S-metolachlor, sebuthylazine, secbumeton, sethoxydim, siduron, simazine, n, simetryn, SMA, sodium arsenite, sodium azide, sodium chlorate, sulcotrione, sulfallate, sulfentrazone, eturon, sulfosulfuron, sulfuric acid, sulglycapin, swep, TCA, tebutam, tebuthiuron, tefuryltrione, tembotrione, tepraloxydim, terbacil, terbucarb, terbuchlor, terbumeton, terbuthylazine, ryn, tetrafluron, thenylchlor, thiazafluron, pyr, thidiazimin, thidiazuron, thiencarbazone-methyl, thifensulfuron, thiobencarb, tiafenacil, tiocarbazil, tioclorim, tolpyralate, topramezone, tralkoxydim, triafamone, tri-allate, triasulfuron, triaziflam, tribenuron, tricamba, triclopyr, tridiphane, trietazine, trifloxysulfuron, trifludimoxazin, trifluralin, sulfuron, trifop, l O trifopsime, trihydroxytriazine, trimeturon, tripropindan, tritac, tritosulfuron, ate, and xylachlor. [0043J Another embodiment of the t disclosure is a method for the control or prevention of fungal attack. This method comprises ng to the soil, plant, roots, foliage, or locus of the fungus, or to a locus in which the infestation is to be prevented (for example applying to cereal or grape plants), a fungicidally effective amount of one or more of the compounds of Formula L The compounds are suitable for treatment of various plants at fungicidal levels, while exhibiting low oxicity. The compounds may be useful both in a protectant and/or an eradicant fashion. 100441 The compounds have been found to have significant fungicidal effect particularly for agricultural use. Many of the compounds are particularly ive for use with agricultural crops and horticulturalplants. [0045J It will be understood by those skilled in the art that the efficacy of the compound for the foregoing fungi establishes the general utility of the compounds as ides. [0046J The compounds have broad ranges of activity against fungal pathogens. Exemplary ens may include, but are not limited to, causing agent of wheat leaf blotch (Zymoseptoria lritic.:i), wheat brown rust (Puu.:inia tritil:ina), wheat stripe rust inia slriiformis), scab of apple (Venturia inaequalis), powdery mildew of grapevine (Uncinula necator), barley scald (Rhynchosporium secalis), blast of rice (Pyricularia oryzae), rust of soybean (Phakopsora pachyrhizi), glume blotch of wheat (Leptosphaeria nod.arum), powdery mildew of wheat (Blumeria isf sp.tritici), powdery mildew of barley (Blumeria graminisf sp. hordei), powdery mildew of cucurbits (Erysiphe cichoracearum), anthracnose of cucurbits (Colletotrichum lagenarium), leaf spot of beet spora beticola), early blight of tomato (Alternaria solani), and spot blotch of [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan barley (Cochlioho/11s .,ativ11.\) The exact amount of the active material to be applied is dependent not only on the specific active material being applied, but also on the particular action d, the fungal species to be lled, and the stage ofgrmvth thereof as well as the part of the plant or other t to be contacted with the compound. Thus, all the compounds, and ations ning the same, may not be equally effective at similar concentrations or against the same fungal species. [00471 The compounds are effective in use with plants in a disease-inhibiting and phytologically acceptable amount The term "disease-inhibiting and phytologically acceptable amount" refers to an amount of a compound that kills or inhibits the plant disease for which control l 0 is desired, but is not icant!y toxic to the plant This amount will generally be from about 0.1 to about 1000 ppm (parts per million), with 1 to 500 ppm being preferred. The exact concentration of compound required varies with the fungal disease to be controlled, the type offormulation employed, the method of application, the particular plant species, climate conditions, and the like. A le application rate is typically in the range from about O IO to about 4 pounds/acre (about O O I to 0.45 grams per square meter, g/m2). 100481 Any range or desired value given herein may be e:--;tended or altered without losing the effects sought, as is apparent to the skilled person for an understanding ofthe teachings herein. 100491 The compounds ofFormula I may be made using well-known chemical procedures.
Intermediates not specifically mentioned in this disclosure are either cially available, may be made by routes disclosed in the chemical literature, or may be readily synthesized from commercial starting materials utilizing standard procedures.
GENERAL SCHEMES [00501 The following schemes rate approaches to generating picolinamide compounds of Formula L The following descriptions and examples are provided for rative purposes and should not be construed as limiting in terms of substituents or substitution patterns.
Compounds of Formula 1.1, wherein R3 and R12 are as originally defined and are equivalent, can be prepared by the methods shown in Scheme 1, step a. The compound of Formula 1.0 can be treated with an organometallic nucleophile such as phenylmagnesium bromide (PhMgBr) in a polar aprotic solvent such as tetrahydrofuran (THF) at a temperature of [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan about 0 °C to 23 °C to afford compounds of Formula 1.1, Vvherein R1 and R12 are as previously defined, as shown in a.
Scheme 1 CH3 CH3 ?0 ------>- (PMB)Bno (PMS)BnO?:? OEt R3 1.0 1 .1 100521 Compounds of Formula 2.2, wherein R, is as ally defined and may or may not be equal to R12, can be prepared by the methods shown in Scheme2, steps a - c. Compounds of a 2.2, wherein R3 and R12 are as previously defined but not an electron-deficient aryl or heteroaryl group and may or may not be equivalent, can be obtained by treating the nds of a 2.0, wherein R, and R12 are as previously defined but not an electron-deficient aryl or heteroaryl group and may or may not be equivalent, with a mixture of a hydride reagent, such as triethylsilane (Et3SiH), and an acid, such as 2,2,2-trifluoroacetic acid (TFA) in a halogenated solvent such as dichloromethane (DCM) at a temperature of about 0 °C to 23 °C, as depicted in a. Alternatively, compounds of Formula 2.1, wherein R3 and R12 are an electron-deficientaryl or heteroaryl group and may or may not be equivalent, can be obtained by treating the compounds of a 2.0, wherein R3 and R12 are an electron-deficient aryl or heteroaryl group and may or may not be equivalent, with a base, such as sodium hydride (NaH), and a st, such as imidazole, in a polar aprotic t such as THF at a temperature of about 23 °C, followed by sequential addition of carbon disulfide (CS2) and an alkyl iodide, such as thane (I\IeI), as depicted in b. Compounds of Formula 2.2, wherein R3 and R12 are an electron-deficient aryl or heteroaryl group and may or may not be equivalent, can be obtained by treating the compounds of Formula 2.1, wherein R3 and R12 are as previously defined and may or may not be equivalent, with a tin reagent, such as tributyltin hydride, and a radical initiator, such as azobisisobutyronitrile (AIBN), in a nonpolar t such as toluene at a temperature of about 115 °C, as ed inc.
Scheme2 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan (0053] Compounds of Formula 3. I, wherein R, and R12 are as originally defined and may or may not be equivalent, can be prepared according to the method outlined in Scheme 3, step a.
Compounds of Formula 3.1, wherein R1 and R 12 are as originally defined and may or may not be equivalent, can be prepared from nds of Formula 3.0, wherein R3 and R12 are as previously defined and may or may not be lent, by ng with a base, such as NaH and an alkyl halide, such as Mel, in a polar aprotic solvent like N,N-dimethylformamide (DMF) at a temperature of about O °C to 23 °C, as depicted in a.
Scheme 3 _,,l a ? R12 (PMB) BnO , ?OH Compounds of Formula 4.1, wherein R3 and R12 are as originally defined and may or may not be equivalent, can be prepared according to the method outlined in Scheme 4, step a.
Compounds of Formula 4.1, wherein R3 and R12 are as originally d and may or may not be equivalent, can be prepared from compounds of Formula 4.0, wherein R3 and R12 are as previously defined and may or may not be equivalent, by treating with a fluorination reagent, such as (diethylamino)sulfur trifluoride (DAST), in a nated solvent such as DCM at a temperature of about O °C to 23 °C, as depicted in a.
[Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Scheme 4 Bn0?=12 (00551 Compounds of Formula 5.3, wherein R3, R4, and R12 are as originally defined and R3 may or may not be equivalent to R12, can be prepared ing to the methods outlined in Scheme 5, steps a - c. Compounds of Formula 5.3, wherein R1, R4, and R 12 are as originally defined and R3 may or may not be equivalent to R12, can be prepared from compounds of a 5.0, wherein R1, R4, and R12 are as originally defined and R, may or may not be equivalent to R12, by treating with a catalyst such as palladium on carbon (Pd/C) in a e of an unsaturated hydrocarbon solvent, such as cyclohexene, and a polar protic solvent, such as ethanol (EtOH), at an elevated temperature of about 65 °C, as shown in a. Alternatively, compounds of Formula 5.3, wherein R3 and R12 are an electron-deficient aryl or heteroaryl group and may or may not be equivalent and R4 is hydroxyl (OH) or alkoxy, can be obtained by treating nds of Formula 5.1, wherein R3,?, and R12 are as previously defined and R3 may or may not be equivalent to R12, with a mixture of a hydride reagent, such as Et1SiH, and an acid, such as TFA in a halogenated solvent such as DCM at a temperature of about O °C to 23 °C, as indicated in h. Additionally, compounds of Formula 5.3, wherein R1 and R12 are as originally defined but not an electron-deficient aryl or heteroaryl group and may or may not be equivalent, and? is a proton (H), can be obtained by treating the nds of Formula 5.2, n R3, R4, and R12 are as previously defined and R3 may or may not be equivalent to R12, with a mixture of a e reagent, such as Et3SiH, and an acid, such as TFA in a halogenated t such as DCM at a temperature of about O °C to 23 °C, as depicted in c.
Scheme 5 [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan CH3 CH3 CH3 BnO?R 12 PMBO?R PMBO?R12 R4 R4 OH R3 R3 R3 .0 5.1 5.2 a b C Compounds of Formula 6.2, wherein R3 and R12 are an electron-deficient aryl or heteroaryl group and equivalent, can be prepared ing to the methods outlined in Scheme 6, steps a -b. Compounds of Formula 6.1, wherein R3 and R12 are as described previously, can be prepared from compound of Formula 6.0, by treating with an aryl bromide, such as 4- bromobenzonitrile, in the presence of a Pd catalyst, such as XPhos Pd G3 (CAS # 14450851 commercially available from Sigma-Aldrich), in a polar aprotic solvent such as THF at a IO temperature of about 55 °C, as ted in a Compounds of Formula 6.2, wherein R1 and R 12 are as described previously, can be prepared from compound of Formula 6.1, wherein R3 and R12 are as described previously, by treating with a hydride reagent, such as borane yl sulfide complex, in the presence of a catalyst, such as (R)-(+)Methyl-CBS-oxazaborolidine, in a polar protic solvent, such as methanol (MeOH), at a temperature of about O °C, as indicated in b.
Scheme 6 0 CH3 A0 a b R12 R12 H3CAy HO? H3C CH3 R3 R3 6.0 6.1 6.2 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Compounds of Formula 7.2, wherein R3 and R12 are as originally defined and equivalent, can be prepared according to the methods outlined in Scheme 7, steps a - h.
Compounds of Formula 7.1, wherein R3 and R12 are as described usly, can be prepared from compounds of Formula 7.0, by treating with a catalyst, such as SbCls, in a halogenated t such as DCM at a temperature of about 23 °C, as indicated in a. Compounds of Formula 7.2, wherein R, and R 12 are as described previously, can be prepared from compound ofFormula 7.1, n R3 and R12 are as described previously, by treating with a hydride reagent, such as borane dimethyl sulfide complex, in the presence of a catalyst, such as (R)-(+)Methyl-CBS- oxazaborolidine, in a polar protic solvent, such as methanol (MeOH), at a temperature of about 23 °C, as ted in b.
Scheme 7 OH 0 CH3 H3C a b ?R12 ?R12 ?R12 R3 HC3 HO CH3 CH3 CH3 OH R3 R3 7.0 7.1 7.2 [0058J Compounds of Formula 8.1, wherein n is either 0 or 1, and Wis either CH2 or 0, can be prepared according to the method outlined in Scheme 8, step a. Compounds of Formula 8.1, wherein n is either O or I, and Wis either CH2 or 0, can be prepared from compounds of Formula 8.0, wherein n is either 0 or 1, and Wis either CH2 or 0, by treating with a base, such as yllithium Li), and an aldehyde, such as acetaldehyde, in a polar aprotic solvent such as THF at a temperature of about -78 °C to 23 °C, as indicated in a.
Scheme 8 a HO [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Compounds of Formula 9.1, n R3 and R12 are as originally defined, can be prepared according to the method outlined in Scheme 9, step a. Compounds of Formula 9.1, wherein R3 and R12 are as originally defined, can be prepared from compounds of a 9.0, wherein R,is as originally defined (Formula 9.0 is either commerically available, or could be prepared from asymmetric Shi epoxidation of the corresponding £-olefin precursor, as reported in Wang, Z.-X.; Tu, Y.; Frohn, M.; Zhang, J.-R: Shi, Y. .! Am. ('hem. Soc. 1997, I 19, 11224), by treating with a pre-mixed suspension of a copper(!) salt, such as copper iodide (Cul), and an organometallic nucleophile, such as 4-(trifluoromethyl)phenylmagnesium bromide in a polar aprotic solvent such as THF, at a temperature of about -78 °C to 23 °C, as shown in a.
Scheme 9 .,,,R12 9.0 9.1
[0060] nds of Formula 10.2, n R1, R2, R3, R4 and R12 are as originally d, can be prepared according to the method outlined in Scheme 10, step a Compounds of Formula 10.0, wherein R1 is as originally d, can be treated with ls of Formula 10.1, wherein R2, R3, R-1 and R 12 are as originally defined, and a coupling reagent such as 3- (ethyliminomethyleneamino)-N,N-dimethylpropanamine hydrochloride (EDC), and a catalyst such as N,N-dimethylpyridinamine (DMAP) in a halogenated solvent like DCM to afford compounds of Formula 10.2, wherein R1, R2, R3, R-i and R12 are as previously defined, as shown 1n ll.
Scheme 10 + ,,. R12 -a HO.A, - 'f-R4 10.0 10.1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan 10061 J Compounds of Formula 11.2, wherein R1, R2, R,, R4, Re" R12 and Z are as ally defined, can be prepared according to the methods outlined in Scheme 11, steps a - b. As ed in a, compounds of Formula 11.2, wherein R 1, R2, R1, R4 and R12 are as ally defined, can be subjected to an acid, such as a 4 normal (N) on of hydrogen chloride (HCl) in dioxane, in a halogenated solvent such as DCM to afford compounds of Formula 9.0, \vherein R1, R2, R3, ? and R12 are as originally defined, as shown in a. [00621 Compounds of Formula 11 0, wherein R1, R2, R1, R4 and R12 are as originally defined, can be treated with compounds of Formula 11.1, n R6 and Z are as originally defined, in the presence of a base, such as diisopropylethylamine ), and a peptide l O coupling reagent, such as benzotriazolyl-oxytripyrrolidinophosphonium hexafluorophosphate (PyBOP), in an halogenated solvent like DCM, to afford compounds of Formula 11.2, wherein R,, R2, R,, R4, Re,, R12 and Z are as originally defined, as shown in b.
Scheme 11 ?z?OH 11.2 11.1 Compounds of a 12.0, wherein R1, R2, R3, ?' &,, R7, R12 and Z are as originally defined, can be prepared according to the method outlined in Scheme 12, step a. As shown in a, compounds of Formula 11.2, wherein R1, R2, R3, R4, R6, R12 and Z are as originally defined, can be treated with an appropriate alkyl halide with or without a reagent such as sodium iodide (Nal) and an alkali carbonate base, such as sodium carbonate (Na2C03) or potassium 1002106834 carbonate (K2CO3), in a solvent like acetone at a temperature of about 55 °C, or by treatment with an acyl halide in the presence of an amine base, such as pyridine, ylamine (Et3N), DMAP, or mixtures thereof, in an aprotic solvent such as DCM, at a temperature of about 23 °C, to afford compounds of Formula 12.0 wherein R1, R2, R3, ?, ?, R7, R12 and Z are as originally defined.
Scheme 12 - IY6 Rs R7 o R2 a ?::2 0 R1 R3 11.2 12.0 EXAMPLES [0064) The chemistry in the following examples may be conducted using either enantiomer of2-((tert-butoxycarbonyl)amino)propanoic acid (Boe-Ala-OH) or either protected (PMB or Bn) or ected enantiomer ofethyl lactate.
[0065] Example 1: Preparation of (S)(benzyloxy)- l,1-bis(4-fluorophenyl)propan - BnO [0066) To a solution of (S)-ethyl2-(benzyloxy)propanoate (2.08 grams (g), 10.0 millimoles (mmol)) in ydrofuran (THF; 20 milliliters (mL)) at O °C was slowly added (4- fluorophenyl)magnesium bromide (31.3 mL, 25.0 mmol, 0.8 molar (M) in THF) over a 10 minute (min) period. The reaction vessel was d to warm slowly to room temperature over 2 hours (h), and the reaction mixture was quenched by careful addition of ted (sat.) aqueous (aq.) ammonium chloride (N?Cl; 50 mL). The mixture was diluted with diethyl ether (Et2O; 50 mL), 1002106834 the phases were separated, and the aq. phase was extracted with Et2O (2 x 50 mL). The combined organic phases were washed with sat. aq. sodium chloride (NaCl, brine; 100 mL), dried over sodium sulfate (Na2SO4), filtered, and concentrated. The resulting oil was purified by flash column chromatography (silica gel (SiO2), O?5% acetone in hexanes) to afford the title compound (3.28 g, 93%) as a colorless oil: 1H NMR (300 MHz, CDCh) 8 7.47- 7.38 (m, 2H), 7.38 -7.27 (m, 5H), 7.17-7.09 (m, 04-6.89 (m, 4H), 4.64 (dd, J= 11.4, 0.7 Hz, lH), 4.51-4.38 (m, 2H), 3.12 (s, lH), 1.11 (d, J= 6.1 Hz, 3H); 19FNMR (376 MHz, CDCh) 8 -116.19, -116.41; ESIMS m/z 377 ([M+Nat).
[0067] Example 2A: Preparation of (S)-4,4'-(2-(benzyloxy)propane-l,1- diyl)bis(fluorobenzene).
F F BnO - BnO F F To a solution of (S)(benzyloxy)-1,1-bis(4-fluorophenyl)propanol (709 rams (mg), 2.00 mmol) in dichloromethane (DCM; 20 mL) at O °C was added triethylsilane (Et3SiH; 3.19 mL, 20.0 mmol) followed by 2,2,2-trifluoroacetic acid (TFA; 1.53 mL, 20.0 mmol).
The mixture was stirred at O °C for 1 h. The resulting on was quenched by careful on of sat. aq. sodium bicarbonate (NaHCO3; 20 mL). The phases were separated, and the aq. phase was extracted with DCM (2 x 30 mL). The combined organic phases were washed with brine (50 mL), dried over , filtered, and concentrated. The resulting oil was ed by flash column chromatography (Si 02, o? 10% acetone in hexanes) to afford the title compound (627 mg, 92%) as a white solid: 1H NMR (400 MHz, CDCb) 8 7.31- 7.22 (m, 5H), 7.21-7.16 (m, 2H), 7.10-7.03 (m, 2H), 7.00-6.91 (m, 4H), 4.54 (dd, J= 11.5, 0.7 Hz, 1H), 4.31 (dd,J= 11.6, 0.8 Hz, lH), 4.14 (dq, J= 8.1, 6.1 Hz, IH), 3.93 (d, J= 8.1 Hz, lH), 1.18 (d, J= 6.0 Hz, 3H); 19FNMR (376 MHz, CDCh) 60, -117.10; ESIMS (m/z) 361 ([M+Nat).
Example 2B: Preparation of (S)-(2-(benzyloxy)-l -methoxypropane-1,1- diyl)dibenzene. 1002106834 BnO - BnO To a suspension of sodium hydride (NaH; 52.0 mg, 1.30 mmol, 60% weight per weight (w/w) in mineral oil) inN,N-dimethylformamide (DMF; 3 mL) at 0 °C was added a solution of(S)(benzyloxy)-l,l-diphenylpropanol (318 mg, 1 mmol) in DMF (1 mL). The reaction mixture was stirred at room temperature for 30 min and then cooled to O 0C. Iodomethane (Mel; 93.0 iters (µL), 1.50 mmol) was added, and the on mixture was stirred at room temperature for l h. The resulting solution was quenched by careful addition of sat. aq. NaHCO3 (10 mL). The mixture was diluted with diethyl ether (Et2O; 10 mL), the phases were separated, and the aq. phase was extracted with Et2O (2 x 10 mL). The combined organic phases were washed with brine (20 mL), dried over Na2SO4, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO2, 0?5% acetone in hexanes) to afford the title compound (295 mg, 89%) as a colorless oil: 1H NMR (400 MHz, CDCh) 87.47- 7.41(m, 2H), 7.40- 7.35 (m, 2H), 7.33- 7.18 (m, llH), 4.69 (d,J= 11.9 Hz, lH), 4.54 (d,J= 12.3 Hz, lH), 4.50 (q, J= 6.1 Hz, lH), 3.13 (s, 3H), 1.10 (d,J= 6.1 Hz, 3H); 13CNMR(l01 MHz, CDCh) 8142.96, 141.31, 138.79, , 128.54, 128.14, 127.61, , 127.08, 126.95, 126.69, 99.99, 85.35, 78.13, 70.80, 52.46, 13.65; ESIMS (mlz) 333 ([M+Ht).
[0071] e 2C: Preparation of (S)-(2-(benzyloxy)-l-fluoropropane-l,1- diyl)dibenzene.
BnO - BnO To a solution of (benzyloxy)-l,l-diphenylpropanol (300 mg, 0.942 mmol) in DCM (5 mL) at O °C was added (diethylamino)sulfur trifluoride (DAST; 1.88 mL, 1.88 mmol, 1 Min DCM). The reaction was slowly warmed to room temperature over 3 h. The resulting 1002106834 solution was quenched by careful addition of sat. aq. NaHCO3 (5 mL). The phases were separated, and the aq. phase was extracted with DCM (2 x 10 mL). The combined organic phases were washed with brine (10 mL), dried over Na2SO4, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO2, O?10% acetone in hexanes) to afford the title compound (300 mg, 98%) as a colorless oil: 1H NMR (400 MHz, CDC'3) 87.58-7.49 (m, 2H), 7.43-7.37 (m, 2H), 7.36-7.20 (m, 9H), 7.09-6.99 (m, 2H), 4.47 (d, J= 11.7 Hz, lH), 4.37- 4.25 (m, 2H), 1.26 (dd,J= 6.3, 1.3 Hz, 3H); 13C NMR (101 MHz, CDC13) 8 142.23 (d, J= 22.7 Hz), 141.00 (d,J= 23.5Hz), 138.03, 128.21, 128.16, 127.90 (d, J= 1.5 Hz), 127.80, 127.72 (d, J= 1.7 Hz), 127.52, 127.42 (d,J= 1.3 Hz), 126.23 (d,J= 9.6 Hz), 125.93 (d,J= 8.7 Hz), 99.96 (d,J= 180.8Hz), 78.91 (d,J= ), 71.68, 14.47 (d,J= 3.6Hz); 19FNMR(376 MHz,CDCh)8- 159.80.
Example 2D, Step 1: Preparation of(S)-O-(2-(benzyloxy)-l,l-bis(3,4,5- trifluorophenyl)propyl) yl carbonodithioate.
F F BnO F BnO F F F F To a solution of (S)(benzyloxy)-l, l-bis(3,4,5-trifluorophenyl)propanol (496 mg, 1.16 mmol) in anhydrous THF (5.8 mL) was added NaH (93.0 mg, 2.33 mmol), followed by ole (3.96 mg, 0.0580 mmol), and the reaction mixture was stirred at ambient temperature for 1 h. Carbon disulfide (562 µL, 9.30 mmol) was added via syringe in one portion, followed by Mel (579 µL, 9.30 mmol), and the reaction mixture was stirred at ambeint ature for 2 h. The reaction mixture was diluted with Et2O (5 mL) and quenched with sat. aq. NH4Cl (10 mL). The layers were separated, and the aq. layer was ted with Et2O (3 x 10 mL). The ed organic layers were dried over magnesium sulfate (MgSO4), filtered and concentrated to afford an orange/brown oil. The crude oil was purified by flash column tography (SiO2, 0?50% ethyl acetate (EtOAc) in hexanes) to afford the title nd (627 mg, 94%) as a clear, bright yellow colored oil: 1H NMR (400 MHz, CDC'3) 8 7.40-7.27 (m, 3H), 7.24-7.16 (m, 2H), 7.02 (dd, J= [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan 1002106834 9.1, 6.6 Hz, 2H), 6.96 (dd, J=8.8, 6.5 Hz, 2H), 5.44 (q, J= 6.1 Hz, lH), 4.66 (d, J= 11.6 Hz, lH), 4.51 (d, J= 11.6 Hz, lH), 2.49 (s, 3H), 1.16 (d, J= 6.1 Hz, F NMR (376 MHz, CDCb) 8- 133.89 (d, J= 20.7 Hz), -134.73 (d, J= 20.6 Hz), -159.83 (t,J= 20.6 Hz), -160.56 (t, J= 20.7 Hz); (Thin film) 2922, 1721, 1622, 1595, 1526, 1436, 1344, 1241, 1217, 1197, 1119, 1088, 1040, 965, 908,861, 822, 730, 712, 697, 672 cm-1• e 2D, Step 2: Preparation of (S)-5,5'-(2-(benzyloxy)propane-1,1- diyl)bis(1,2,3-trifluorobenzene).
F F BnO BnO F F F F A solution of(S)-O-(2-(benzyloxy)-1,1-bis(3,4,5-trifluorophenyl)propyl) S- methyl carbonodithioate (598 mg, 1.16 mmol) in toluene (200 mL) was degassed by a freezepump-thaw procedure (3 cycles using liquid nitrogen (N2)) under an here ofN2• Tributyltin e (3.12 mL, 11.6 mmol) was then added, the reaction flask was fitted with a reflux condenser, and the reaction mixture was heated to a light reflux (115 °C). A solution ofazobisisobutyronitrile (AIBN; 0.200 g, 1.22 mr..101) in degassed toluene (3 cycles via liquidN2; 32 mL) was added via syringe down the reflux condenser over 3 h. Once slow addition ofthe AIBN was te, the reaction e was stirred at reflux overnight. The solvent was removed in vacuo to provide a pale yellow oil. The crude oil was purified by flash column chromatography (SiO2, 0?30% EtOAc in hexanes) to afford the title compound (358 mg, 72%) as a clear, colorless oil:1H NMR ( 400 MHz, CDCb) 8 7.28 (d,J= 6.6 Hz, 3H), 7.17 - 7.06 (m, 2H), 6.92 (dd, J= 8.5, 6.5 Hz, 2H), 6.79 (dd,J= 8.3, 6.4 Hz, 2H), 4.59 (d, J= 11.7 Hz, lH), 4.31 (d, J= 11.7 Hz, lH), 4.02 (p, J= 6.2 Hz, lH), 3.76 (d,J= 6.8 Hz, lH), 1.19 (d, J= 6.1 Hz, 3H);19F NMR (376 MHz, CDCb) 8-133.80 (d, J = 20.5 Hz), -134.34 (d, J= 20.5 Hz), -162.54 (t,J= 20.5 Hz), -162.84 (t, J= 20.5 Hz); (Thin film) 2871, 1621, 1526, 1445, 1345, 1262, 1235, 1116, 1096, 1043, 859,802, 728, 698, 679 cm-1• [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan 1002106834 e 3A: Preparation of (S)-1, I-bis(4-fluorophenyl)propanol.
F F BnO HO F F
[0078] To a solution of(S)-4,4'-(2-(benzyloxy)propane-l,1-diyl)bis(fluorobenzene) (575 mg, 1.70 mmol) in ethanol (EtOH; 11 mL) and cyclohexene (5.5 mL) at room temperature was added palladium on carbon (Pd/C; 362 mg, 0.0850 mmol, 2.5% w/w ofPd). The reaction mixture was stirred at 65 °C for 2 h, cooled to room temperature, ed through a plug of Celite®, and concentrated to afford the title compound (415 mg, 98%) as a colorless oil: 1H NMR (400 MHz, CDC'3) 8 7.36-7.29 (m, 2H), .18 (m, 2H), 7.09-6.93 (m, 4H), 4.47 (dqd, J= 8.2, 6.1, 3.3 Hz, IH), 3.80 (d, J= 8.3 Hz, IH), 1.55 (d, J= 3.3 Hz, IH), 1.19 (d, J= 6.1 Hz, 3H); 13C NMR (101 MHz, CDC'3) 8162.90 (d, J= 23.3 Hz), 160.46 (d, J= 23.1 Hz), 138.15 (d, J= 3.1 Hz), 136.94 (d, J= 3.6 Hz), 130.14 (d, J= 7.8 Hz), 129.55 (d,J= 7.8 Hz), 115.70 (d,J= 18.8 Hz), 115.49 (d, J= 18.8 Hz), 70.07, 58.61, 21.63; 19F NMR (376 MHz, CDC' 3) 8-115.84, -116.19.
Example 3B: Preparation 1,1-bis(2-fluorophenyl)propane-1,2-diol.
To a solution of (S)-1,1-bis(2-fluorophenyl)((4-methoxybenzyl)oxy)propan- 1-ol (790 mg, 2.06 mmol) in DCM (20 mL) at O °C was added Et3SiH (3.28 mL, 20.6 mmol) followed by TFA (1.57 mL, 20.6 mmol). The mixture was stirred at O °C for 1 h. The resulting solution was quenched by careful addition of sat. aq. NaHCO3 (20 mL). The phases were separated, and the aq. phase was extracted with DCM (2 x 30 mL). The combined organic phases were washed with brine (50 mL), dried over Na2SO4, filtered, and concentrated. The ing oil was purified by flash column chromatography (Si02, O?10% acetone in hexanes) to afford the title 1002106834 nd (388 mg,71%) as a colorless oil:1H NMR (400 MHz,CDCh)o 7.90- 7.77 (m,lH), 7.70 (tt,J= 8.2,1.5 Hz,lH),7.31- 7.10 (m,4H),6.97 (ddd,J= 12.7,8.1,1.3 Hz,IH),6.88 (ddd,J =11.8,8.0,1.4 Hz,lH),5.11 (qd,J= 6.3,2.3 Hz,lH),3.49 (s,lH),2.27 (s,1H),1.09 (d,J= 6.3 Hz,3H); 19F NMR (376 MHz,CDC1 = 8.3 Hz),-113.92 (d,J= 8.4 Hz); ESIMS 3) o -112.90 (d,J (m/z) 551 ([2M+Nat). e 3C: Preparation of(S)-1,1-bis(4-bromophenyl)propanol.
Br Br PMBO - HO Br Br
[0082] To a solution of (S)-1,1-bis(4-bromophenyl)((4-methoxybenzyl)oxy)propan- 1-ol (1.80 g,3.56 mmol) in DCM (18 mL) at O °C was added Et3SiH (5.68 mL,35.6 mmol) followed by TFA (2.72 mL,35.6 mmol). The mixture was warmed slowly to room temperature over 3 h. The resulting solution was quenched by careful addition of sat. aq. NaHCO3 (20 mL). The phases were separated,and the aq. phase was ted with DCM (2 x 30 mL). The combined organic phases were washed with brine (50 mL),dried over Na2SO4, filtered,and concentrated. The resulting oil was purified by flash column tography (Si02, o?10% acetone in hexanes) to afford the title compound (742 mg,56%) as a colorless oil: 1H NMR (300 MHz,CDCh)o 7.51- 7.36 (m,4H),7.25- 7.17 (m,2H),7.18- 7.06 (m,2H),4.48 (dq,J= 8.2,6.1 Hz,lH),3.76 (d,J= 1H),2.80(s,lH), 1.19(d,J=6.2Hz,3H);13CNMR(75MHz,CDCh)o ,139.85, 131.98,131.85,130.39,129.84,121.06,120.72,69.82,58.91,21.65; (Thin film) 3390, 3024, 2969, 2900,1486,1072 cm-1• Example 3D, Step 1: Preparation of(S)-1,1-bis(4-((trimethylsilyl)ethynyl)- phenyl)propanol. 1002106834 HO HO To a solution of(S)-1,1-bis(4-bromophenyl)propanol (1.01 g,2.72 mmol) in THF (9 mL) was added bis(triphenylphosphine)palladium dichloride (0.095 g,0.136 mmol) and copper(!) iodide (Cul; 0.026 g,0.136 mmol). The mixture was sparged withN2 for 20 min, and triethylamine (Et3N; 4.53 mL) was added dropwise. To the resulting mixture was added ethynyltrimethylsilane (1.15 mL, 8.15 mmol) dropwise,and the mixture was heated to reflux and d overnight. The mixture was cooled to room temperature, and the reaction was quenched with sat. aq. NaHCO3 • The products were extracted with EtOAc (2x), and the combined organic layers were washed with brine, dried over Na2SO4, ed and concentrated. The crude e was then purified by flash column chromatography (SiO2, 0?20% acetone in hexanes) to provide the title compound (495 mg,45%) as a brown foam: 1H NMR (400 MHz, CDCb) o 7.48-7.42 (m,2H), 7.42-7.37 (m, 2H), 7.33-7.27 (m, 2H), 7.24- 7.17 (m,2H), 4.51 = 12.2,6.1, 3.5 Hz, lH), 3.81 (d, J= 8.3 Hz, lH), 1.60 (d,J= 3.8 Hz,lH),1.18 (d,J= 6.1 Hz, 3H),0.26 (s,9H),0.26 (s, 9H);13C NMR (101 MHz, CDC'3) o 142.55,141.48,132.42, 132.29, 128.69, 128.15,121.90, 121.57, , 104.71, 94.33,69.76,59.96,21.55, 0.00; (Thin flm) 3397, 2960,2156, 1501,1248,861,840 cm-1; HRMS-ESI (m/z) [M+Ht calcd for C25H33OSb, 405.2064; found, 405.2070.
[0085] Example 3D, Step 2: Preparation of (S)-1,1-bis(4-ethynylphenyl)propanol.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan HO HO ....CH3 H3C... 'CH3 To a solution of(S)-1, 1-bis(4-((trimethylsilyl)ethynyl)phenyl)propanol (0.470 g, 1.16 mmol) in methanol (MeOH; 5.8 mL) was added potassium carbonate (K.2CO3; 0.482 g, 3.48 mmol). The mixture was stirred for 1 hat room temperature and then filtered through Celite®. The filter cake was washed with MeOH, and the filtrate was concentrated. The crude material was purified by flash column chromatography (SiO2, 0?20% acetone in hexanes) to provide the title compound (288 mg, 95%) as a yellow oil: 1H NMR (300 MHz, CDCh) o 7.48- 7.43 (m, 2H), 7.43 - 7.39 (m, 2H), 7.35 - 7.29 (m, 2H), 7.24- 7.19 (m, 2H), 4.51 (dqd, J= 8.3, 6.1, 3.7 Hz, lH), 3.82 (d, J= 8.3 Hz, lH), 3.05 (s, IH), 3.04 (s, IH), 1.63 - 1.55 (m, IH), 1.18 (d, J= 6.1 Hz, 3H); 1 3C NMR (101 MHz, CDCh) o 142.84, 141.82, 132.60, 132.48, 128.74, 128.22, 120.87, 120.57, 83.31, 83.29, 77.39, 77.29, 69.73, 59.96, 21.66; (Thin film) 3436, 3280, 2968, 2106, 1499, 1075, 825 cm-1; HRMS-ESI (mlz) [M+Ht calcd for C19H17O, 261.1274; found, 261.1272.
Example 3D, Step 3: Preparation 1, 4-ethylphenyl)propanol.
?.::CH1/ HO HO To a solution of (S)-1,1-bis(4-ethynylphenyl)propanol (0.144 g, 0.553 mmol) in EtOAc (2.8 mL) was added palladium (5% weight (wt) on carbon, dry basis; 0.235 g, 0.055 mmol). The mixture was d under a balloon ofhydrogen overnight. The e was filtered 1002106834 through Celite®, and the filter cake was washed with EtOAc. The combined filtrate was then concentrated, and the crude residue was purified by flash column tography (SiO2, 0?25% acetone in hexanes) to provide the title compound (97.0 mg, 65%) as a clear oil: 1HNMR (400 MHz, CDC'3) 8 7.33-7.25(m, 2H), 7.22-7 .15 (m, 2H), .11 (m, 2H), 7.10 (d, J= 8.1 Hz, 2H), 4.51 (dqd, J= 8.7, 6.1, 2.5 Hz, lH), 3.74 (d, J= 8.9 Hz, IH), 2.65 -2.53 (m, 4H), 1.68 (d, J= 2.8 Hz, lH), 1.23-1.14 (m, 9H); 13C NMR (101 MHz, CDC'3) 8 142.74, 142.33, , 138.91, 128.48, 128.40, 128.07, 128.02, 70.19, 60.02, 28.41, 28.39, 21.37, 15.47, 15.46;(Thin film) 3421, 2963, 1510, 1110, 821 cm-1; HRMS-ESI (m/z) t) calcd for C19H24NaO, 291.1719; found, 291.1 725.
Example 3E: Preparation of l-(9H-xanthenyl)ethanol.
To a solution of 9H-xanthene(364 mg, 2.00 mmol) in THF (10 mL) at -78 °C was added n-butyllithium (2.5 M in hexanes; 0.880 mL, 2.20 mmol). The mixture was stirred at -78 °C for 30 min. Acetaldehyde (0.226 mL, 4.00 mmol) was added, and the reaction mixture was warmed slowly to room temperature ght. The resulting solution was quenched by careful addition of sat. aq. NH4Cl (10 mL). The phases were separated, and the aq. phase was extracted with Et2O (2 x 15 mL). The combined organic phases were washed with brine (20 mL), dried over Na2SO4, filtered, and concentrated. The resulting oil was purified by flash column chromatography (Si02, o?10% acetone in hexanes) to afford the title compound (216 mg, 48%) as a colorless oil: 1H NMR (400 MHz, CDC'3) 8 7.33-7.22 (m, 4H), 7.17-7.04 (m, 4H), 3.99 (d, J= 5. l Hz, lH), 3.96-3.82(m, lH), 1.54(d,J= 6.0 Hz, IH), l.00(d,J= 6.3Hz, 3H); 13CNMR(I01 MHz, CDC'3)8152.94, 152.65, 129.54, 129.30, 128.19, 128.17, 123.18, 123.14, 122.48, 121.73, , 116.41, 73.07, 47.06, 18.81; ESIMS (m/z) 475 ([2M+Nat).
Example 3F: ation of(1S,2S)-l -phenyl(4- (trifluoromethyl)phenyl)propanol. !002106834 To a mixture ofmagnesium turnings (102 mg, 4.20 mmol) in Et2O (4 mL) was added 1-bromo(trifluoromethyl)benzene (0.588 mL, 4.20 mmol) at room ature, followed by Mel (5 µL). Upon warming to a gentle boil using a heat gun, the mixture turned a yellow/brown color. The reaction was then stirred in a water bath at room temperature for 30 min until almost all the ium was consumed. This was added to a suspension ofcopper(!) iodide (Cul; 400 mg, 2.10 mmol) in Et2O ( 4 mL) at -78 °C. The reaction was stirred at -20 °C for 30 min, then cooled to - 78 °C, and (2S,3S)methylphenyloxirane (0.201 mL, 1.50 mmol) was added. The resulting IO mixture was warmed slowly to room temperature overnight. The resulting solution was quenched by l addition of sat. aq. NH4Cl (10 mL). The phases were separated, and the aq. phase was extracted with Et2O (2 x 15 mL). The combined c phases were washed with brine (20 mL), dried over Na2SO4, filtered, and concentrated. The resulting oil was purified by flash column chromatography (Si02, O? I0% e in hexanes) to afford the title compound (390 mg, 94%) as a light yellow oil: 1H NMR (400 MHz, CDCh) 8 7.60- 7.50 (m, 2H), 7.48- 7.38 (m, 2H), 7.38- 7.33 (m, 4H), 7.30- 7.23 (m, IH), 4.58 (dqd,J= 8.4, 6.1, 3.5 Hz, IH), 3.88 (d, J= 8.5 Hz, IH), 1.65 (d,J= 3.6 Hz, lH), 1.20 (d,J= 6.1 Hz, 3H); 19F NMR (376 MHz, CDCb) 8 -62.49; ESIMS (mlz) 263 ([M-OH]l, [0093) Example 3G, Step 1: Preparation of4,4'-(2-oxopropane-l,1-diyl)dibenzonitrile.
To a suspension of 4-bromobenzonitrile (546 mg, 3.00 mmol) and cesium carbonate (977 mg, 3.00 mmol) in THF (10 mL) under anN2 atmosphere was added acetone (1.10 mL, 15.00 mmol), followed by X-Phos Pd 03 (50.8 mg, 0.060 mmol). Then, the vial was sealed and heated to 55 °C for 4 days. The reaction was diluted with EtOAc (30 mL) and washed with sat. 1002106834 NH4Cl (3 x 10 mL), water (15 mL), and brine (15 mL). Then the organic phase was dried over , filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO2, 0?40% EtOAc in hexanes) to affordthe title compound (174 mg, 22%) as a colorless oil: 1HNMR (400 MHz, CDCh) 8 7.66 (d, J= 8.4 Hz, 4H), 7.34 (d, J= 8.3 Hz, 4H), 5.21 (s, IH), 2.29 (s, 3H); 13C NMR (101 MHz, CDCb) 8 203.68, 142.15, 132.75, 129.64, 118.21, , 64.25, .43; ESIMS m/z 261 ([M+Ht).
Example 3G, Step 2: Preparation of (S)-4,4'-(2-hydroxypropane-1,1- diyl)dibenzonitrile.
CN CN CN CN To a solution of 4,4'-(2-oxopropane-l,1-diyl)dibenzonitrile (174 mg, 0.668 mmol) in e (4.5 mL) was added (R)methyl-3,3-diphenylhexahydropyrrolo[l,2- c][l,3,2]oxazaborole (1 M solution in toluene, 66.8 µL, 0.067 mmol). Then, the on was cooled to O °C and a solution of BH3-DMS (69.8 µl, 0.735 mmol) in 0.5 mL toluene was added over 2 min. The flask was left to stir at O °C. After 2 h, the reaction was quenched with methanol (0.5 mL), diluted with EtOAc and added water. Phases were separated and the aqueous phase was extracted with EtOAc x 2. The combined organic phases were washed with brine (20 mL), dried overNa2SO4, filtered, and trated. The resulting oil was purified by flash column chromatography (Si02, 0?50% EtOAc in hexanes) to afford the title compound (99.7 mg, 57%) as a colorless oil: 1HNMR (400 MHz, CDCh) 8 d 7.60 (dd,J = 8.4, 6.8 Hz, 4H), 7.51-7.46 (m, 2H), 7.43 -7.37 (m, 2H), 4.63-4.47 (m, lH), 3.97 (d, J= 7.5 Hz, lH), 1.97 (d, J = 3.8 Hz, lH), 1.21 (d, J= 6.2 Hz, 3H). 13C NMR (101 MHz, CDCh) 8 146.91, 145.86, 132.60, 132.45, 129.90, 129.19, , 118.51, 110.96, 110.92, 69.19, 59.56, 22.27; ESIMS m/z 263 ([M+Ht).
[0097] Example 3H, Step 1: Preparation of 3,3-diphenylbutanone. 1002106834 To a magnetically stirred mixture of 2,3-diphenylbutane-2,3-diol (500 mg, 2.06 mmol) in DCM (10 mL) was added antimony hloride (26.5 µL, 0.206 mmol) under air atmosphere. The on mixture was stirred at 25 °C for 1 h and then was quenched by slow addition of sat. aq. NaHCO3• The ing mixture was diluted with water and additional DCM, and the organic layer was ted by passing through a phase separator. The resulting oil was purified by flash column chromatography (SiO2, 0?5% acetone in hexanes) to afford the title compound (330 mg, 71%) as a ess oil: 1HNMR (400 MHz, CDCb) 8 7.36-7.31 (m, 4H), 7.30- 7.25 (m, 2H), .15 (m, 4H), 2.11 (s, 3H), 1.87 (s, 3H); 13C NMR (101 MHz, CDCh) 8 209.16, 143.59, 128.36, 126.91, 62.32, 27.62, 26.42; ESIMS m/z 225 ([M+H]l.
Example 3H, Step 2: Preparation of (S)-3,3-diphenylbutanol.
To a solution of 3,3-diphenylbutanone (150 mg, 0.669 mmol) in toluene (4.5 mL) was added (R)-l-methyl-3,3-diphenylhexahydropyrrolo[l,2-c][l,3,2]0xazaborole (1 M solution in toluene, 134 µL, 0.134 mmol). Then, a solution ofBH3-DMS (70.2 µL, 0.702 mmol) in 0.5 mL oftoluene was added to the reaction mixture over 2 min. The flask was left to stir at room temperature. After 1 h, the reaction was quenched with ol (0.5 mL). DCM and water were added, and the phases were separated. The aqueous phase was ted with DCM (2x). The combined organic phases were washed with brine (20 mL), dried over Na2SO4, filtered, and concentrated. The resulting oil was purified by flash column chromatography (SiO2, 0?20% acetone in hexanes) to afford the title compound (150 mg, 99%) as a colorless oil: 1HNMR (400 MHz, CDCl3) 8 d 7.39 - 7.17 (m, lOH), 4.70-4.61 (m, lH), 1.67 (s, 3H), 1.51 (d,J= 4.9 Hz, lH), 1.11 (d, J= 6.3 Hz, 3H); 13C NMR (101 MHz, CDCh) 8 147.30, 145.86, 128.40, 128.15, 128.05, 127.79, 126.20, 126.01, 72.28, 51.77, 23.26, 18.39; ESIMS mlz 227 ([M+Ht).
Example 31, Step 1: Preparation of(S)-l,l-bis(2,3-dimethoxyphenyl)propane- 1,2-diol. ,...,..o To a solution ofisopropylmagnesium lithium chloride (1.3 Min THF, 6.1 mL, 8.00 mmol) was added THF (2 mL) and l-bromo-2,3-dimethoxybenzene (1.74 g, 8.00 mmol). The resulting brown solution was heated to a gentle reflux (75 °C external temp) for 2.5 h, then cooled to O °C in an ice water bath. (S)-methyl 2-hydroxypropanoate (0.191 ml, 2 mmol) was then added dropwise via syringe. The reaction was stirred at O °C for 1 h, then removed from the cold bath and stirred overnight at rt. The reaction was cooled to O °C in an ice water bath, diluted with water (20 mL), brine (20 mL), and Et20 (40 mL), and was quenched with 1 N HCI (8 mL). The phases were separated, and the aqueous phase was ted with EhO (20 mL). The c phases were ed, dried over MgS04, filtered, and concentrated to provide an oil. Purification by automated silica gel column chromatography (5-50% EtOAc in hexanes) provided the title compound (568 mg, 82%) as a yellow, crystalline solid: 1H NMR (300 MHz, CDCb) 8 7.43 (td, J= 8.0, 1.5 Hz, 2H), 7.11 (td, J= 8.1, 4.9 Hz, 2H), 6.83 (dd, J= 8.1, 1.4 Hz, 2H), 5.06 -4.82 (m, lH), 4.74 (d, J= 1.2 Hz, lH), 3.81 (s, 3H), 3.80 (s, 3H), 3.20 (s, 3H), 3.04 (s, 3H), 2.86 (d, J= 9.5 Hz, lH), 0.97 (d, J= 6.4 Hz, 3H); 13C NMR (126 MHz, CDCb) 8 152.89, 152.82, 146.94, 145.53, 139.56, 138.92, 123.32, 123.26, 122.01, , 111.30, 79.20, 77.22, 60.07, 59.26, 55.77, 55.64, 18.34; HRMS-ESI (mlz) ([M+Nat) calcd for C19H2406Na, 371.1465; found, 371.1456.
Example 31, Step 2: Preparation of 1, 2,3-dimethoxyphenyl)propanone.
HO - 0 .,.....o .,.....o 0 0 I I 1002106834 To a solution of (S)-1,1-bis(2,3-dimethoxyphenyl)propane-l ,2 -diol (560 mg, 1.61 mmol) in anhydrous CH2Ch (8 mL) at O °C was added triethylsilane (770 µl,4.82 mmol) and trifluoroacetic acid (TFA, 124 µL,1.61 mmol). The resulting solution was stirred at O °C for 2 h, then removed from the cold bath and stirred for 2 h. TFA (248 µL,3.2 mmol) was added,and the reaction was then stirred overnight at rt. The reaction was d with water (25 mL) and extracted with CH2Ch (3x 25 mL). The organic extracts were dried over Na2S04,filtered,and concentrated to provide an oil. Purification by automated silica gel column chromatography (5-25% acetone in hexanes) provided the title compound (396 mg,75%) as a white solid: 1H NMR (300 MHz,CDC13) 8 6.99 (t,J= 8.0 Hz,2H),6.87 (dd,J= 5 Hz,2H),6.67 -6.54 (m,2H),5.86 (s,lH),3.87 (s, 6H),3.75 ,2.25 (s,3H); 13C NMR (126 Ch) 8 207.18,152.69, 147.02, 132.23, ,121.61,111.64,60.36,55.74, 51.96, 29.80; HRMS-ESI(m/z) ([M+Na]l calcd for C19H2205Na,353.1359; found,353.1353.
Example 31, Step 3: Preparation of l,l-bis(2,3-dimethoxyphenyl)propanol. 0 - HO ,,,,.o ,,,,.o I 0 ] To a solution of 1,1-bis(2,3-dimethoxyphenyl)propanone (356 mg,1.08 mmol) in methanol (3.5 mL) was added sodium borohydride (61 mg,1.6 mmol). The ing solution was stirred at rt for 20 h,then was quenched with sat'd NHiCl (1 mL),diluted with water (20 mL) and extracted with CH2Ch (3x 20 mL). The organic extracts were combined,dried over Na2S04,filtered,and concentrated to provide the title compound (360 mg,100%) as an oil: 1H NMR(300 MHz,CDCb) 8 7.16-6.88 (m,4H),6.79 (ddd,J= 9.6,7.8,1.9 Hz,2H),4.81 (d,J= 8.3 Hz,lH),4.53-4.32 (m,lH),3.84 (s,3H),3.84 (s,3H),3.77 (s,3H),3.76 (s,3H),2.04 (d,J= 4.2 Hz,lH),1.22 (d,J= 6.2 Hz,3H); 13C NMR (126 Ch) 8 152.98,152.83,147.71, 147.04,136.17,135.33,123.94,123.62,120.96,120.84,110.76,110.48,70.32,60.26,60.20,55.66, 55.63,45.11,21.80; tfilm) 3451,2935,2833,1582,1473,1428,1266, 1215, 1167,1125, 1088, 1068,1004,964,908,835,809,787,748,728. 1002106834 Example 4A: Preparation (S)-1,1-diphenylpropanyl 2-((tert- butoxycarbonyl)amino)-propanoate.
BocHN,,,,.(o BocHN HO ,,,,rOH + CH3
[00108] To a on of (S)-1,1-diphenylpropanol (317 mg, 1.493 mmol) in DCM (15 mL) at O °C were added (S)((tert-butoxycarbonyl)amino)propanoic acid (Boe-Ala-OH; 311 mg, 1.64 mmol) andN,N-dimethylpyridinamine (DMAP; 18.2 mg, 0.149 mmol) followedbyN1- ((ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride (EDC; 573 mg, 2.99 mmol), and the reaction e was stirred at room temperature overnight and concentrated to give a yellow oil. The crude material was purified by flash column chromatography (Si02, 1?10% acetone in hexanes) to afford the title compound (433 mg, 75%) as a colorless oil: 1H NMR (400 MHz, CDCb)87.42-7.07 (m, l0H), 5.80 (dq, J= 10.1, 6.1 Hz, lH), 4.97 (d,J= 8.0 Hz, lH), 4.19 -4.06 (m, 1H), 4.03(d,J= 10.1 Hz, lH), 1.41 (s,9H), 1.23 (d,J=6.l Hz, 3H), 0.76(d,J=7.2Hz, 3H); 13CNMR(101MHz,CDCb)8172.83, 154.96, , 141.26, 128.79, 128.50, 128.10, 128.08, 126.91, 126.67, 79.62, 73.10, 57.98, 49.21, 28.33, 19.31, 17.98; ESIMS m/z 384 ([M+H]l.
Example 5, Step 1: Preparation of(S)(((S)-l,l-diphenylpropanyl)oxy)-l- oxopropanaminium chloride.
BocHN,,,,.fO
[00110] To a solution of (S)-(S)-1,l-diphenylpropanyl 2-((tertbutoxycarbonyl )amino)propanoate (Cmpd 2; 433 mg, 1.13 mmol) in DCM (6 mL) was added a 4 N solution ofHCI in dioxane (2.8 mL, 11.3 mmol), and the mixture was stirred for 3 h at room temperature. The solvent was evaporated under a stream ofN2 to provide the title compound (360 mg, 100%) as a white solid: ESIMS (mlz) 284 ([M+Ht). 1002106834 Example 5, Step 2: Preparation of(S)-(S)-1,1-diphenylpropanyl 2-(3- hydroxymethoxypicolinamido)propanoate.
Cl H3N,,,'(Jl, 0 -
[00112] To a solution of (S)(((S)-l,1-diphenylpropanyl)oxy)oxopropan m de (Cmpd 46; 361 mg, 1.13 mmol) and oxymethoxypicolinic acid (210 mg, 1.24 mmol) in DCM (11 mL) were added benzotriazolyl-oxytripyrrolidinophosphonium hexafluorophosphate (PyBOP; 646 mg, 1.24 mmol) and N-ethyl-N-isopropylpropanamine (DIPEA; 0.651 mL, 3.72 mmol), and the reaction mixture was stirred for 2 hat room temperature.
The solvent was evaporated and the crude oil was purified by flash column chromatography (Si02, 1?50% acetone in hexanes) to afford the title compound (340 mg, 70%) as a white foam: 1H NMR (400 MHz, CDCb) 8 12.10 (s, lH), 8.34 (d, J= 8.0 Hz, lH), 7.98 (d, J= 5.2 Hz, lH), 7.38-7.06 (m, l0H), 6.86 (d, J= 5.3, lH), 5.83 (dq, J= 10.1, 6.1 Hz, lH), 4.52 (dq, J= 8.1, 7.2 Hz, lH), 4.06 (d, J= 10.2 Hz, lH), 3.93 (s, 3H), 1.26 (d, J= 6.1 Hz, 3H), 0.97 (d, J= 7.2 Hz, 3H); 3C NMR (101 MHz, CDCb) 8 171.67, 168.53, 155.34, 148.72, 141.38, 141.13, 140.40, 130.48, 128.80, 128.50, 128.10, , 126.95, 126.70, 109.39, 73.57, 57.93, 56.07, 47.85, 19.24, 17.61; HRMS-ESI (m/z) ([M+Ht) calcd for C25H27N205, 435.1920; found, 435.1925.
Example 6A: ation of(S)-(S)-1,1-diphenylpropanyl 2-(3-acetoxy ypicolinamido)propanoate.
To a solution of (S)-(S)-1,l-diphenylpropanyl 2-(3-hydroxy methoxypicolinamido)-propanoate (Cmpd 90; 70.0 mg, 0.161 mmol), Et3N (44.9 µL, 0.332 mmol), 1002106834 and DMAP(3.94 mg, 0.032 mmol) in DCM (3.2 mL) was added acetyl chloride (17.2 µL,0.242 mmol) at room temperature,and the reaction mixture was stirred for 2 h. The solvent was evaporated,andthe resulting crude oil was ed by flash column chromatography (Si02, 1?40% acetone in hexanes) to afford the title compound (75.0 mg,97%) as a colorless oil: 1H NMR(4OOMHz,CDC'3)o8.41 (d,J= 7.8 Hz,IH),8.3O(d,J= 5.4Hz,lH), 7.38-7.lO(m,lOH), 6.97 (d,J= 5.4 Hz, lH),5.82 (dq,J= 10.0,6.2 Hz,1H),4.52 (dt,J= 8.2,7.1 Hz,lH), 4.05(d,J= .1 ,3.87 (s, 3H),2.37(s,3H),1.24 (d,J= 6.1 Hz, 3H),0.89(d,J= 7.1 Hz,3H); 13C NMR (101 C'3) o 172.23,168.89,162.28, 159.42,146.66,141.55,141.44,141.25, 137.45, 128.77,128.50,128.13,128.11,126.89,126.67,109.73,73.32,57.90,56.27,47.85,20.75, 19.25,17.92; SI (mlz) ([M+Ht) calcd for C27H29N206,477.2025; found,477.2019.
Example 6B: Preparation of(S)-(S)-1,1-diphenylpropanyl 2-(3- (acetoxymethoxy)methoxypicolinamido)propanoate.
To a suspension of (S)-(S)-1,l-diphenylpropanyl 2-(3-hydroxy methoxypicolinamido)-propanoate (Cmpd 90; 100 mg,0.230 mmol) and K2C03 (63.6 mg,0.460 mmol) in acetone (4.6 mL) was added bromomethyl acetate (33.9 µL,0.345 mmol) at room temperature,and the mixture was heated to 55 °C for 3 h and then cooled to room temperature. The solvent was evaporated and the resulting crude material was ed by flash column chromatography(Si02,1?40% acetone in hexanes) to afford the title compound(94.0 mg,80% yield) as a colorless oil: 1H 0 MHz,CDC'3) o 8.25 (d,J= 5.4 Hz,lH), 8.22 (d,J= 7.9 Hz, lH), 7.34-7.09 (m, !OH),6.92 (d, J= 5.4 Hz,lH),5.83 (dq, J= .2 Hz,lH),5.72 (d,J= 0.7 Hz,2H),4.60 -4.49 (m,lH),4.06(d,J= 10.1 Hz,lH), 3.88(s,3H),2.05(s,3H),1.25 (d, J= 6.1 Hz,3H),0.91(d,1= 7.2 Hz,3H); (101 MHz,CDC'3) o 172.33,170.25,162.88,160.24, 145.70,143.91, 142.54,141.48,141.25,128.76,128.49,128.12,128.09,126.89,126.65, 109.56, 1002106834 89.50, 73.27, 57.92, 56.17, 48.07, 20.86, 19.25, 17.73; HRMS-ESI (m/z) [M+Ht calcd for C2sH31N207, 507.2131; found, 507.2125.
Example 6C: Preparation of(S)-(S)-1,1-diphenylpropanyl 2-(3- ( (isobutyryloxy)methoxy)methoxypicoIinamido)propanoate.
To a solution of (S)-(S)-1,1-diphenylpropanyl 2-(3-hydroxy methoxypicolinamido)-propanoate (Cmpd 90; 100 mg, 0.230 mmol) in acetone (4.6 mL) were added sodium carbonate (Na2C03; 73.2 mg, 0.690 mmol), sodium iodide (Nal; 6.90 mg, 0.046 mmol) and chloromethyl 2-ethoxyacetate (62.9 mg, 0.460 mmol). The mixture was heated to 55 °C overnight and then cooled to room temperature, and the solvent was evaporated. The resulting residue was ed by flash column chromatography (S i02, 2?30% acetone in hexanes) to afford the title compound (79.0 mg, 64%) as a colorless oil: 1H NMR (400 MHz, CDCh) o 8.28 (d, J= 7.9 Hz, IH), 8.25 (d, J= 5.3 Hz, lH), 7.36-7.08 (m, lOH), 6.92 (d, J= 5.4 Hz, IH), 5.83 (dq, J= 10.1, 6.2 Hz, lH), 5.79-5.69 (m, 2H), 4.62-4.44 (m, lH), 4.06 (d, J= 10.1 Hz, lH), 3.86 (s, 3H), 2.53 (hept, J= 7.0 Hz, lH), 1.25 (d, J= 6.2 Hz, 3H), 1.13 (d, J= 7.0 Hz, 6H), 0.91 (d, J= 7.2 Hz, 3H); 1 3CNMR(lO1 MHz, CDC' 3) 8176.22, , 162.85, 160.23, 145.55, 144.16, 142.18, 141.48, 141.26, 128.76, 128.49, 128.12, 128.09, , 126.65, 109.48, 89.90, 73.26, 57.93, 56.12, 48.07, 33.85, 19.26, 18.68, 17.74; HRMS-ESI (m/z) ([M+H]l calcd for C30H35N207, 535.2444; found, Example A: tion ofFungicidal ty: LeafBlotch of Wheat (Zymoseptoria i; Bayer code SEPTTR):
[00120] Technical grades of materials were dissolved in acetone, which were then mixed with nine volumes ofwater (H20) containing 110 ppm Triton X-1OO. The fungicide solutions were 1002106834 applied onto wheat seedlings using an automated booth sprayer to f. All sprayed plants were allowed to air dry prior to further handling. All fungicides were evaluated using the aforementioned method for theiractivity vs. all target diseases, unless stated otherwise. Wheat leaf blotch and brown rust activity were also evaluated using track spray applications, in which case the fungicides were formulated as EC formulations, containing 0.1% Trycol 5941 in the spray solutions.
Wheat plants (variety Yuma) were grown from seed in a ouse in 50% mineral 0% soil-less Metro mix until the first leaf was fully emerged, with 7-10 seedlings per pot. These plants were inoculated with an aqueous spore suspension of Zymoseptoria tritici either prior to or after fungicide treatments. After inoculation the plants were kept in 100% relative humidity (one day in a dark dew chamber followed by two to three days in a lighted dew chamber at 20 °C) to permit spores to ate and infect the leaf. The plants were then transferred to a greenhouse set at 20 °C for disease to develop. When disease symptoms were fully expressed on the 1st leaves of untreated plants, infection levels were assessed on a scale of0 to 100 percent disease severity. Percent disease control was calculated using the ratio of disease ty on treated plants relative to untreated plants.
] Example B: Evaluation of Fungicidal Activity: Wheat Brown Rust (Puccinia triticina;Synonym: Puccinia recondita f. sp. tritici; Bayer code PUCCRT): Wheat plants (variety Yuma) were grown from seed in a greenhouse in 50% mineral soil/50% soil-less Metro mix until the first leaf was fully emerged, with 7-10 seedlings per pot. These plants were inoculated with an aqueous spore sion of Puccinia triticina either prior to or after fungicide ents. After inoculation the plants were kept in a dark dew room at 22 °C with 100% relative humidity overnight to permit spores to germinate and infect the leaf. The plants were then transferred to a ouse set at 24 °C for e, to develop. Fungicide formulation, application and e ment followed the procedures as described in the Example A.
Example C: Evaluation of Fungicidal Activity: Wheat Glume Blotch (Leptosphaeria nodorum;Bayer code ):
[00125] Wheat plants (variety Yuma) were grown from seed in a greenhouse in 50% mineral soil/50% soil-less Metro mix until the first leaf was fully emerged, with 7-10 seedlings per pot. These plants were inoculated with an aqueous spore suspension of Leptosphaeria nodorum 24 1002106834 h after ide treatments. After inoculation the plants were kept in 100% ve humidity (one day in a dark dew chamber followed by two days in a lighted dew chamber at 20 °C) to permit spores to ate and infect the leaf. The plants were then transferred to a greenhouse set at 20 °C for disease to develop. Fungicide formulation, application and disease ment followed the procedures as described in the Example A. [00126) Example D: Evaluation ofFungicidal ty: Apple Scab (Venturia inaequalis; Bayer code VENTIN): [00127) Apple seedlings (variety McIntosh) were grown in soil-less Metro mix, with one plant per pot. Seedlings with two expanding young leaves at the top (older leaves at bottom ofthe plants were trimmed) were used in the test. Plants were inoculated with a spore suspension of Venturia inaequalis 24 h after fungicide treatment and kept in a 22 °C dew r with I00% ve ty for 48 h, and then moved to a greenhouse set at 20 °C for disease to develop.
Fungicide formulation, application and disease assessment on the sprayed leaves followed the procedures as described in the Example A. [00128) Example E: Evaluation ofFungicidal Activity: LeafSpot ofSugar Beets (Cercospora betico!a; Bayer code CERCBE): [00129) Sugar beet plants (variety HH88) were grown in soil-less Metro mix and trimmed regularly to in a uniform plant size prior to test. Plants were inoculated with a spore suspension 24 h after fungicide treatments. Inoculated plants were kept in a dew chamber at 22 °C for 48 h then incubated in a greenhouse set at 24 °C under a clear plastic hood with bottom ation until disease symptoms were fully expressed. Fungicide formulation, application and disease assessment on the sprayed leaves followed the procedures as described in the Example A. [00130) Example F: Evaluation of Fungicidal Activity: Asian n Rust (Phakopsorapachyrhizi; Bayer code PHAKPA): [00131) Technical grades ofmaterials were ved in acetone, which were then mixed with nine volumes ofH2O containing 0.011 % Tween 20. The fungicide solutions were applied onto soybean seedlings using an automated booth sprayer to run-off. All sprayed plants were allowed to air dry prior to further handling. 1002106834 [00132) n plants ty ms 82) were grown in soil-less Metro mix, with one plant per pot. Two weeks old seedlings were used for testing. Plants were inoculated either 3 days prior to or 1 day after fungicide treatments. Plants were incubated for 24 h in a dark dew room at 22°C and 100% relative humidity then transferred to a growth room at 23 °C for e to develop. Disease severity was assessed on the sprayed leaves. [00133) Example G: Evaluation ofFungicidal Activity: Barley Scald (Rhyncosporium s; Bayer code RHYNSE): [00134) Barley seedlings (variety Harrington) were propagated in soil-less Metro mix, with each pot having 8 to 12 plants, and used in the test when the fir?t leaf was fully emerged. Test plants were inoculated by an aqueous spore suspension ofRhyncosporium secalis 24 h after fungicide treatments. After inoculation the plants were kept in a dew room at 22°C with 100% relative humidity for 48 h. The plants were then transferred to a greenhouse set at 20 °C for disease to develop. Fungicide formulation, application and e assessment on the sprayed leaves followed the procedures as described in the Example A. [00135) Example H: Evaluation ofFungicidal Activity: Rice Blast (Pyricularia oryzae; Bayer code ): [00136) Rice seedlings (variety Japonica) were propagated in soil-less Metro mix, with each pot having 8 to 14 , and used in the test when 12 to 14 days old. Test plants were inoculated with an aqueous spore suspension ofPyricularia o,yzae 24 h after fungicide treatments.
After inoculation the plants were kept in a dew room at 22°C with 100% relative humidity for 48 h to permit spores to germinate and infect the leaf. The plants were then transferred to a greenhouse set at 24 °C for disease to develop. Fungicide formulation, application and disease assessment on the sprayed leaves followed the procedures as described in the Example A. [00137) Example I: Evaluation ofFungicidal Activity: Tomato Early Blight (Alternaria solani; Bayer code AL TESO): ) Tomato plants (variety Outdoor Girl) were ated in ess Metro mix, with each pot having one plant, and used when 12 to 14 days old. Test plants were inoculated with an aqueous spore suspension ofAlternaria solani 24 h after ide treatments. After inoculation the plants were kept in a dew room at 22 °C with I00% relative humidity for 48 h to permit spores 1002106834 to germinate and infect the leaf. The plants were then transferred to a growth room at 22 cc for disease to develop. Fungicide formulation, application and disease assessment on the sprayed leaves followed the procedures as described in the Example A.
[00139] e J: Evaluation ofFungicidal Activity: Cucumber cnose (Colletotrichum lagenarium; Bayer code COLLLA): Cucumber seedlings (variety Bush Pickle) were propagated in soil-less Metro mix, with each pot having one plant, and used in the test when 12 to 14 days old. Test plants were inoculated with an aqueous spore suspension ofColletotrichum lagenarium 24 hr after fungicide treatments. After inoculation the plants were kept in a dew room at 22 cc with 100% relative ty for 48 hr to permit spores to germinate and infect the leaf. The plants were then transferred to a growth room set at 22 cc for disease to develop. Fungicide formulation, application and disease assessment on the sprayed leaves followed the procedures as bed in the Example [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Table 1. Compound Structure, Preparation Method, and Appearance Prepared *Crnpd. According Structure Appearance No. To H3C O ?'' f ,,, Example l; 0 Example H 3C::Y Y \:Vhitc Solid CH 3 0 CH 3 3A: Example 4A 0 Example l; H3C O ?'' f ,,, Example 0 2A: 2 H 3C::Y Y Colorless Oil CH 3 0 CH 3 Example 0 e l; H3C O ?" ,,, Example ,., f 0 2A: _, H 3C::Y Y Colorless Oil CH 3 0 CH 3 E:--;ample Example 4A H,C Example l; OY?'' f ,,, 0 Example H 3C::Y 2A: Clear, 4 CH 3 0 CH 3 Example Colorless Oil E:--;arnple 4A 0 E:--;ample I: H3C O ?" ,,, f Example 0 2B; H 3C::Y Y Colorless Oil CH 3 0 CH 3 Example Example 4A ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 0 Example l; ::?:Y o Y?'"·? Example o 28: 6 Colorless Oil CH3 0 CH3 Example Example I: O Y?'"·? 0 : :?:Y Example 7 CH3 0 CH3 F Colorless Oil Example Example 4A 0 Example l; H3C O '' ?,,. Example 0 2C: 8 H3C:Y Y ess Oil CH3 0 CH3 Example 0 'CH3 Example I; ::?>(o!(?" ?o Example CH3 0 CH3 2A: 9 Colorless Oil Example Example 4A 0 Example l; ? Example H3C O '' ?,,. 2A; 0 Colorless Oil H3C:Y Y Example CH3 0 CH3 3A; Example 4A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example 0 Example 1: Example C O 11 ,,, 0 2A; Colorless Oil H3C H3 Y Y ?''f e CH3 0 CH3 Example 4A C O ,,, 0 Example 12 H3CH3 Y Y?''f 3E: Colorless Oil CH3 0 CH3 Example 4A Example 13 ::?Y0Y?,,.. fO 3E: Colorless Oil CH3 0 CH3 Example 4A ::?Y0Y?'"·fO Example I: 14 Example CH3 0 CH3 Colorless Oil Example 4A C O Example I; ,,, 0 Example H3C H3 Y Y?''f ess Oil CH3 0 CH3 3C; Example 4A [Annotation] an None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example ::?Y 0 Example 1: 0 Example CH3 Y?",r 16 0 CH3 Colorless Oil Example Example 4A 0 CH3 ?: ::?Y0Y?'",ro _,,, Example 18 3F: Colorless Oil Example 4A CH3 0 CH3 H3CYOY?" r,,. Example I: 0 Example H3C 2A; 19 CH3 0 CH3 Colorless Oil Example Example 4A :3?y o Example 3 y?Jl0 2A; CH3 0 Clear Oil Example Example 4A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Prepared *Cmpd. According Structure Appearance No. To Example Example 1: :3?:yoy?:(o Example 3 2A: 21 CH3 0 Clear Oil H3C Example Example 4A H3C Example l; O ?:c,,. 0 e HC3 :Y Y 2A: 22 CH3 0 Clear Oil H3C CH3 Example Example 4A Example l; ::?)( 1(?""·¢0 Example ~-)..,) CH3 0 CH3 Clear Oil 1/" I Example CH3 Example 4A Example I: Example 24 Sticky Wax Example 4A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Prepared *Cmpd. According Structure Appearance No. To 0 Example l; H3C O ?'' f,,, Example 0 Sticky Wax H3C)( r( CH3 0 CH3 Example 4A ..,..CH3 H3C O '' f,,, ? 0 Example l; H3C)( r( Example 26 CH3 0 CH3 Sticky Wax Example 4A o Example l; ? o 27 ?:?Y r( " ..f Example Stich Wax CH3 0 CH3 3C: Example 4A Example l; Example 28 Example White Foam 3D, Steps 11 Example 4A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. To 0 CH3 ::?)(o ?,, ?o Example 1: r( Example CH3 0 CH3 3C; 29 Example Sticky Wax . Steps Example 4A 0 CH3 ::?)( o _..,, ?".. ?o Example 31 r( Clear Oil CH3 0 CH3 3F: Example 4A HsC O ?'',,, ( 0 Cl Example l; H3C)( r( ...,..., Example ;):) CH3 0 CH3 White Solid Example 4A ::?)( o ?'.. (o F Example I: 34 CH3 0 CH3 Example White Solid Example 4A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example Example 1: ::?)(ol(?""fo CH3 Example ,., - 2A; .) ) CH3 0 CH3 White Solid Example CH3 Example 4A H,C O t f,,. e l; 0 Example 36 H3C)( y \Vhite Foam CH3 0 CH3 F 38: Example 4A 0 Example I: ::?)( o Example f 2A: Clear, CH3 0 CH3 Example Colorless Oil Example 4A 0 Example I: HsC O ?'' f,,. Example 0 2A: Clear, 38 H3C)( I( CH3 0 CH3 Example Colorless Oil Example 4A [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example Example I: Example 2A: Clear, Example Colorless Oil Example 4A Example l; Example 40 White Foam Example Example 4A H3c ?'' f,,, e l; )( r( 0 Cl e H3C 2A; 43 CH3 0 CH3 White Solid Example Cl Example 4A ? '•-f Example l; ::?)( o r( o F Example 44 CH3 0 CH3 White Solid Example F Example 4A [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 5, 45 White Solid Step 1 Example 5, 46 Colorless Step 1 Oil N ,,,,_ 47 ? O Example 5, Colorless Oil Step 1 N "'•· Example 5, Pale Yello\\ 48 CH3 Step 1 Oil Example 5, 49 Colorless Oil Step I Example 5, 50 Colorless Step 1 Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To E:xa111plc H2N ,, f,,. 51 CH3 F Colorless Oil Step 1 Example 5.
Colorless Oil Step I ,. Jl CH3 Example 5, 53 Colorless Oil Step 1 ,...0 H2N ,, f,,. E:xa111plc 5. 54 0 Colorless Oil Step 1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. To Example H2N ,, f,,, 0 Example 5, 55 Colorless Oil Step 1 H2N ,, f,,, 0 Example 5. (i Colorless Oil CH3 Step I Example 5. 57 Colorless Oil Step I 58 Example 5, ess Oil Step 1 Example 5, 59 Colorless Oil Step 1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example ,. Jl 60 Example 5, CH3 Colorless Oil Step 1 Example 5. 61 White Solid Step I H2N,, Jl Example 5. 63 Colorless Oil 'O Step 1 '•·rCH3 Example 5, 64 Colorless Oil Step 1 ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example Example 5, 65 Sticky Oil Step 1 Example 5, 66 Sticky Oil Step 1 H2N ,, f,,. 0 e 5, 67 Sticky Oil CH3 Step 1 H2N ,, f,,, 68 Example 5, Sticky Wax CH3 Step 1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 69 Sticky Wax Step I Example 5. 70 Sticky Wa:x Step I Example 5, 71 White Solid Step I Example 5, 72 White Solid Step 1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example Example 5, 73 White Solid Step 1 o F H2N ,,,,.? Example 5, H3C White Solid y Step 1 Example 5, 75 White Solid Step 1 Example 5, 77 White Solid Step l Example 5, 78 White Solid Step 1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According ure Appearance No. To Example H2N ,, r,,, 0 Me Example 5, 79 CH3 White Solid Step 1 Example l; H2N ,, r,,, Example 0 ?B: 80 CH3 F Example Sticky Oil Example 5.
Step I H2N ,, r,,, 0 Example 5, 81 Sticky Oil CH3 F Step 1 83 Colorless Oil Step l [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example H2N ,, f,,, 0 Example 5, Clear, CH3 Step I Colorless Oil H2N ,, f,,, 0 Example 5, Clear, CH3 Step I Colorless Oil H2N ,, f,,, 0 Example 5, 86 White Solid CH3 Step I H2N ""· f o Cl Example 5, 87 CH3 White Solid Step 1 [Annotation] an None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 0 Cl H2N ,, f,,. 0 F Example 5, 88 CH3 White Solid Step 1 ¢c; Cl ,....CH3 ?""fo0 Example 5, 89 White Solid Step 2 0 CH3 Example.:\ 90 White Foam Step 2 Example 5, 91 Colorless Oil Step 2 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example ?'"·? Example 5, 92 o \Vhitc Foam Step 2 0 CH3 Example 5, 93 \Vhitc Foam Step 2 Example 5, 95 Colorless Oil Step 2 Example 5, 96 White Foam Step 2 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. To Example 97 ?""? Example 5, Colorless Oil O Step 2 0 CH3 Example 5, 98 Colorless Oil Step 2 ex; 0 H3C.,, 0 F ?""? Example 5, 99 O Colorless Oil Step 2 0 CH3 H3C,ex; 0 Cl Example 5, 100 ?....?o Colorless Oil Step 2 0 CH3 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Prepared *Cmpd. According Structure Appearance No. To Example H3C,o:; Example 5, 101 ?".. ?o Colorless Oil Step 2 0 CH3 Example 5, 102 Colorless Oil Step 2 Example 5, 103 Colorless Oil Step 2 Example 5, 104 Colorless Oil Step 2 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. oc; To Example ?'"·?o Example 5, 105 ess Oil 0 Step 2 Example 5, 106 Colorless Gel Step 2 Example 5. 107 Colorless Gel Step 2 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example Exarnp e ·'·I , c I ()l) ('olorless Oil Step 2 110 Example 5, Clear, Step 2 Colorless Oil Example 5- Clear.
Step 2 Colorless Oil Example 5, Clear, Step 2 Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example Example 5, 113 White Solid Step 2 Example .:\ 11--l- White Solid Step 2 Example 5, 115 White Solid Step 2 ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example OH F ? O Example 5, 116 White Solid Step 2 0 CH3 CH3 ? oc; F 117 ?'"·fo0 Example 5, White Foam Step 2 0 CH3 Example 5, 118 \:Vhite Foam Step 2 Example 5, 119 White Foam Step 2 [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example H3C,oc; O F ?"..fo0 CH3 Example 5, 120 White Foam 0 CH3 Step 2 H3C,oc; 0 Cl 0 CH3 Example 5, 121 White Foam 0 CH3 Step 2 H3C,oc; 122 ?'"·fo Example 5, \\'hite Foam Step 2 0 CH3 F [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example H3C,¢c; :CH1/" t,,?o ID 0 Example 5, CH 3 White Foam Step 2 Example 5, \:Vhite Foam Step 2 Example 5, 125 White Solid Step 2 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example H3Coc; I 0 ?"..fo Example 5, 127 l C \:Vhite Solid Step 2 0 CH3 oc; Cl I 0 ?"..fo F Example .:\ 128 White Solid Step 2 0 CH3 oc; l I 0 ?'"··f 129 o CH3 e 5, White Solid Step 2 0 CH3 oc; CH3 O CH, o Example 5, Clear, 0 CH 3 Step 2 Colorless Oil ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example O F N,,,.?O Example 5, Clear, Step 2 Colorless Oil 0 CH 3 H3C,oc; 0 Cl ?'"·?o Example .:\ Colorless Step 2 Foam 0 CH3 H3C,oc; 0 CH3 t.?00 Example 5, Colorless Step 2 Foam 0 CH3 [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example H3C,0( Colorless 135 0 Example 5, 0 Tackv Semi- Step 2 CH3 Solid H3C,0( ?"--(o0 136 Cl Example 5, White Foam Step 2 0 CH3 H3C,0( ?'"·(o0 137 F Example 5, White Foam Step 2 0 CH3 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According ure Appearance No. To Example Colorless 138 Example 6B Semi-Solid 13lJ Example 6A ess Oil 140 Example 6A White Foam 141 Example 6B White Foam [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To l.:J-2 Example 6C White Foam 143 Example 6A Colorless Oil 14.:J. Example 6B Colorless Oil 145 Example 6A Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example l.:J-6 Example 6B Colorless Oil ].:j.7 Example 6B Colorless Oil l.:J-8 Example 6B Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To 149 Example 6B Colorless Oil 1.50 Example 6A Colorless Oil 1.52 Example 6A Colorless Oil 153 Example 6B Colorless Oil ation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 155 Example 6A Colorless Oil 15h Example hA Colorless Oil 157 Example 6A Colorless Oil 158 Example 6B Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example Example 6B ess Oil 160 Example 6B Colorless Oil 161 Example 6A Colorless Oil 162 Example 6A Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According ure Appearance No. To Example 163 Example 6B Colorless Oil 16-J. e 6B Colorless Oil 165 Example 6A Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 166 Example 6A ess Oil 167 Example 6A Colorless Oil 168 Example 6A Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. To Example 160 Example 6B Colorless Oil 170 Example 6B Colorless Oil 171 Example 6B Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. To 173 Example 6A Colorless Oil 174 Example 6A Colorless Oil 17:'i Example 6B Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example 176 Example 6B Colorless Oil Clear. 178 Example 6B Colorless Oil Clear, 170 Example 6B Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example O CH3 H 0 Clear.
N,,,,fo E:xarnple 6 B Colorless Oil 0 CH3 181 Example 6B White Foam 182 e 6A Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Prepared *Cmpd. According Structure Appearance No. To Example O CH3 H3C, (0 «o F 183 ?_____}lo Example 6 B White Solid 18--l- Example 6B White Solid 185 Example 6B White Solid [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example O CH3 H3C, (0 0 F 1/" H 186 I E:xarn ple 6 B White Solid 0 CH3 CH3 ? H 3c ,0( 0 CH3 187 o Example 6A White Solid 188 Example 6A White Solid [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Exa111plc 189 Example 6A e Solid H3c, 0 CH3 0 F 1/"' I H O CH3 :::-.... N, 190 plc 6A White Solid CH3 ? 191 Example 6B White Foam [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 192 Example 6B \Vhitc Foam 193 e 6B Sticky Wax 194 Example 6B White Foam [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example 195 Example 6B White Foam 196 Example 6B White Foam 197 Example 6B White Foam [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 198 Example 6B Sticky Wax I ()l) e 6B White Solid 201 Example 6B White Solid [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 202 Example 6B White Solid ] Example 6B White Solid [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example 200 Example hA \Vhitc Solid 207 Example 6A White Solid Clear 208 Example 6A Colorless Oil [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example F Slightly 209 Example 6A Cloudy Colorless Oil Slightly 210 Example 6A Cloudy Colorless Oil Clear 211 Example 6C Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example Colorless 212 F Clear Film Example 6C And Opaque Clear F Colorless 213 Example 6A Viscous Oil And Semi­ Solid [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example Clear. 21--l- Example 6B Colorless Oil Pale \ 21:'i Example 6A Pale Yellm\ 216 Example 6A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. To Example Pale Yello\\ 217 Example 6A Pale YellO\\ 218 Example 6B Pale Ycllo\\ 219 Example 6B [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example Pale Yellm\ 220 Example 6B 221 Example 6B White Foam 222 Example 6B White Foam ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example Cl Example 6A \:Vhite Foam 22--l- F Example 6A White Foam Slightly 225 Example 6B Opaque Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. To Example Example 1: F 2D, Steps 1- White Semi­ 226 2: Solid Example Example 4A F Example 5, 227 White Glass Step I F Example 5, Colorless Step 2 Foam F Clear, 229 Example 6A Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure ance No. To Example 230 Clear.
Example 6B F Colorless Oil 232 Example 5, White Semi­ Step 1 Solid Example l; Example Clear.
Colorless Example Viscous Oil Example 4A 234 F Example 1: Clear.
Example 2A; Colorless Oil Example 3A; Example 4A.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by an Prepared According Structure Appearance Example Example l· Clear Example 2A· Colorles; Oil Example 3A: Example 4A: _____ I Example-:_I Clear Example 2A. Colorles? Oil Example 3A Example 4A'.
Example l· Clear Example 2A· es; Oil Example 3A'.
Example 4A: ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 238 F Example l; Slightly Example 2A: Cloudv Example 3A: Colorless Example 4A Viscous Oil 239 F Example l; Slightly Example 2A: Cloudy Example 3A: Colorless Example 4A Viscous Oil 240 Example l; White Foam Example 2A: Example 3A: Example 4A 241 Example 3H ess Oil Steps 1-2; Example 4A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared According ure Appearance Example Example 3G Steps J and' 2: Example F. Example 3G Steps 1 and' 2· E, xample Example 4A Colorless Oil [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Prepared Structure According Appearance Example Example 1.
Cl Example 3c.
Example 4A: Example 1. \\11itc Foam Example 2A.
F Example 3A: Example 4A'.
Example 1. \\nite Foam Example 3C· Cl Example 4A'.
[Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared Structure According ance Example Example 1.
Example 2A· Example 3A: Example 4A: ----- ----r 0 Example 3?G White Foam Steps l and, 2; Example Example 1. White Example 2A· lid Example 3A'.
Example 4A' Example 1. White Example 2A· Semisolid Example 3A'.
Example 4A'.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] an Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 252 Example l; White Example 2A Semisolid Example 3A: ,...CH3 Example 4A 253 Example l; Clear, Example 2A Colorless Oil Example 3A; Example 4A. --l- Example I; Clear, Example 2A Colorless Oil e 3A; Example 4A. 255 Example l; Clear Example 2A Colorles; Oil Example 3A; Example 4A.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To 256 Example l; Clear, Example 2A; Colorless Oil Example 3A: Example 4A 257 Example l; Clear, 0 Example 2A; Colorless Oil o YH,,.fo /CH3 Example 3A: :;?>r e 4A.
CH3 0 CH3H3C 258 CH3 Example 3 L White Foam 0 Example 4A H,,,f o ::?)( CH3 l(0 CH3 /0 259 F Example l; White Foam 0 Example 2A: o Example 3A; o F Example 4A ::?)( )' ?',,.f CH3 0 CH3 0 O 'CH 3 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 260 Example l; Colorless Oil 0 Example 2A; Example 3A: ::?>( o ), J,,, (o CH3 Example 4A CH3 0 CH3H3C 261 CH3 Example I: Colorless Oil 0 Example 2A; o Example 3A; ?,,, (o ::?>( Example 4A.
CH3 0 CH3H3C 262 Example I: Colorless Oil 0 Example 2A; 0 Example 3A; ?,,,fo F ::?>( e 4A.
CH3 0 CH3H3C 263 Example l; Colorless Oil 0 Example 2A: o ?'', ?o ,....CH3 Example 3A; ::?>( 'r( Example 4A CH3 0 CH3 F [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 264 Example l; White Foam e 2A; Example 3A: Example 4A F Example I: Colorless Oil F Example 2A; F Example 3A; Example 4A.
F F 266 Example l; Sticky Wax Example 2A; F Example 3A: Example 4A.
[Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 267 Example l; Sticky .
Example 2A: Example 3A: Example 4A 268 _.....CH3 Example 3 L Oil 0 Example 4A o't(?''· ::?:Y fo CH3 0 CH3 H3C 269 CH3 Example 31, Oil Example 4A o't(?''·· ::?:Y fo CH3 0 CH3 _.....O [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 270 e l; Colorless Oil Example 2A; Example 3A: Example 4A 271 CH3 Example I: Colorless Oil Example 2A; Example 3A; 272 CH3 Example I: Colorless Oil Example 2A; 0 e 3A; Example 4A 'l( ?'',( ::?:Y CH3 0 CH3 ,,..0 0 H3C 'CH3 273 F Example l; Colorless Oil 0 Example 2A; o ,,..CH3 Example 3A; o 0 Y?'',? ::?:Y Example 4A CH3 0 CH3 CH3 F [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Prepared Structure According Appearance Example Example 1.
Example 2A· Example 3A: Example 4A, Example 3F.
Example 4A 27(-, NF Example 3F.
CH3 ,,,,y e 4A 277 F Example 3F· CH3 N,,,y Example 4A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared Structure According Appearance Example Example 3F· Example 4A Example 3p­ Example 4A NF T____ Example 3p- Colorless Oil CH3 .-''y e 4A F e 3p­ CH3 N,,,,y Example 4A ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared According Structure Appearance Example e 3F· Example 4A 283 Example-=-3F=--I Example 4A 284 NF Example 3F· Colorless Oil CH3 Example 4A .-,yo, 285 F Example 3F· CH3 N.-,y Example 4A [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Prepared According Structure Appearance Example Example 3F· Example 4A Example 3F· Colorless Oil Example 4A F Example 3F· White Foam CH 3 ,,,y ? Example 4A 1/" CH3 Example 3F· yellow Stich Example 4A Wax [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. To Example 290 F Example 3F· White Foam CH3 .--,y? Example 4A o....._ 291 Example 3F· yellow Stich Example 4A Wax 292 Example l· Colorless Oil Example 2i e 3A'.
Example 4A. 293 F Example I: Colorless Oil Example 2A· Example 3A'.
Example 4A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared According Structure Appearance Example Example 1.
Example 2A· Example 3A: e 4A, ----­ Example-=-3F=I_ Example 4A Example 3F· Colorless Oil Example 4A ----------- CH 297 Example 3F· Example 4A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Prepared According Structure Appearance Example Example 3F·A Example 4 Example 3F·A CH3 ,,,,y F Example 3p.A Colorless Oil ? Example 4 1/" CH3 Example 3F· Example 4A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared Structure ance Example Example 3F· Example 4A 303 Example 3F.
Example 4A --l- Example 3p.
Example 4A 305 Example 3p. Colorless Oil Example 4A [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared According Structure ance Example Example 3F· Example 4A 307 Example 3F· Example 4A ------ 3087 F Example 3F·T___ _Thick Oil CH3 N,,,,y Example 4A ,::;r F 309 Example 3F-A Colorless Oil Examplc 4 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 310 Example 5, \\11ite Powder Step 1. 311 Example 5, White Powder Step 1.
H3C CH3 312 CH3 e 5, Cleac Step 1. Colorless 0 Thick Oil H2N ,, (,, [Annotation] Mel.Chan None set by an ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 313 F Example 5, \\11ite Powder Step 1. 314 F Example 5 \\11ite Semi­ Step 1. Solid 315 F Example 5 \\11ite Semi­ Step l. Solid 316 Example 5, Clear Glass Step 1.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 317 F Example l; Pale Purple 0 Example 2A: Sticky Wax H2N? Example 3A: . 0 Example 4A, Fi- F Example 5, step I. 318 0 e 5 Colorless Oil Step 1. . 0 319 Example 5. ·white Foam Step I 320 F Example 5, White Foam Step 1 F F [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. To Example 321 0 Example 5, \:Vhite Solid Step 1 Example.:\ Colorless Oil Step 1. . 0 323 Example 5, Yellow Oil Step 1. . 0 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 324 Example 5, Yellow Oil Step 1.
CH3 0 325 e .:\ Yellow Oil Step 1. . 0 CH3 0 326 Example 5, Yellow Oil Step I. - 0 CH3 0 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According ure Appearance No. To Example 327 e 5, White Foam Step 1 328 Example 5, White Foam Step 1 329 Example 5, White Foam Step 1 330 Example 5, White Foam Step 1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example 331 F Example 5, White Foam Step 1 332 F Example 5, Clear, Step 1. Colorless Oil f0 H2N , '· .,....CH3 , 0 0 .,,.., :):):) H3C, Example 5, LightBrmrn 0 Step 1. Oil H2N ,, f'· .,....CH3 0 0 H3C, .,....CH3 0 0 334 CH3 Example 5, Pale Yello\\ Step I. Oil H N , '· .,....CH3 , f0 0 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example 335 e 5, PaleYello\\ Step 1. Oil H2N ,, (,, ,.,..CH3 0 0 336 CH3 Example 5, White 0 Step 1. PowderY H2N ,, ('· ,.,..CH3 Solid 0 0 337 0 Example 5, Clear, 0 'CH3 Step 1. Colorless Oil H2N ,, (,, 0 F 338 0 Example 5, White 0 'CH3 Step I. Powder.
H,N ,, (,, Solid 0 CH3 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To 339 Example 5, Clear, Step 1. Colorless Oil 340 Example 5, White Solid Step 1.
H,N,, ?,, .,....0 341 Example.:\ Thick Oil 0 Step 1.
H2N ,, ?,, 0 CH3 CH3H3C 342 Example 5, White Solid Step I. ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 343 Example 5, \:Vhite Solid Step 1. 344 Example.:\ White Solid Step l. 345 Example 5, \:Vhite Solid Step 1. 346 Example 5, Thick Oil F Step 1.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 347 Example 5, e Solid Step 1. . 0 348 Example .:\ White Solid Step 1. 349 Example 5, Oil Step 1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by an Prepared *Cmpd. According Structure Appearance No. To Example 350 0 Example 5, Oil Step 1 H2N ,, f,. ,.,..CH3 0 0 CH3H3C 351 CH3 Example 5, Oil Step 1 H2N ,, f,, CH3 ,.,..0 352 H3C, Example 5, Colorless Oil 0 Step 1 H2N ,, f,, ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example 353 Example 5, Colorless Oil Step 1 Example 5, Colorless Oil Step 1 355 F Example 5, Colorless Oil -"''Y r'l( Step 1 356 Example.:\ Colorless Oil Step 1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure ance No. To Example 357 Example 5, Colorless Oil Step 1 358 Example 5, Colorless Oil Step 1 359 Example 5, Colorless Oil Step 1 360 Example 5, Colorless Oil Step 1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared Structure According A nce Example ...,y F Colorless CH3 N Foam ,,,y F Example 5 Colorless CH3 N Step 1 ' Foam Example 5 Colorless Oil Step 1 ' Example 5 Step 1 ' [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According ure Appearance No. To Example 365 Example 5, White Foam Step 1 H2N ,, r'· 0 CH3 366 Example 5_ Stich Wax CH3 F Step 1.
H2N? Y - 0 ,.,,, :::::-.,_ CH3 ,.....0 CH3 367 Example 5_ Stich Wax 0 Step l. . 0 368 Example 5_ Stich Wax 0 Step 1. . 0 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example 369 Example 5 Sticky Wax Step I. 370 Example 5 White Foam Step 1 ' 371 Example 5 White Foam Step 1 ' 372 Example 5, White Foam Step 1 ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Prepared Structure According Appearance Example CH3 ('y,,,y 1/"' I ('yF Example 5 White Foam CH3 ,,,y Step 1 ' 1/"' F Example 5 Colorless Oil Step 1 ' Example 5 Colorless Oil Step 1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Prepared According ure Appearance Example Example 5 Thick Oil Step 1. , -r--------- 379 Example 5 \Vhite Solid Step I. 380 Example "i Thick Oil Step 1. -, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared Structure According Appearance Example - ------- 3;8;2 , e 5 White Foam Step 1. __::::::::,.., ________ 383-r F Example 5 White Solid CH3 --···Y Step 1. , ,:;,--- I 38--l- Example 5 \Vhite Foam Step 1. , [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 385 Example 5, White Foam Step 1. 386 H3C, e 5 e White 0 Step 2. Solid And F Clear Oil 0 gH3 0 ? CH3 387 Example 5 !\latte White Step 2. Solid And F Clear Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. To Example 388 Example 5, Clear, Step 2. ess Oil 38lJ Example .:\ Colorless Step 2. Foam 390 Example 5. Colorless Step 2. Foam [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 391 Example 5, Clear, Step 2. Colorless Oil 392 H3C ....__ Example 5, Semi Solid 0 Step 2. 0 F F oc; F 393 .__ Example 5, White Foam Step 2. ?0cH ,.,,o [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According ure Appearance No. To Example 394 Example 5 Colorless Step 2. Foamy Oil 395 Example 5, White Foam Step 2. 396 H3C, Example 5, White Foam 0 Step 2 ?,,'(Jl'O 0 CH3 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To 397 Example 5, White Foam F Step 2 F F 398 Example 5, \:Vhite Foam Step 2 399 Example 5, White Foam Step 2.
[Annotation] Mel.Chan None set by Mel.Chan ation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 400 H3C,oc; Example 5, White Foam 0 Step 2. 0 ? CH3 0 401 H3C, Example .:\ White Foam 0 Step 2. «o Cl 0 ? CH3 0 402 H3C,oc; Example 5, \:Vhite Foam 0 Step 2. 0 ? CH3 0 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 403 H3C,oc; H3C, Example 5, Colorless Oil 0 0 Step 2 a F ?''·f 0 CH3 CH3 F 40--l- H3C,oc; Example 5, Colorless Oil Step 2 a 0 ?'•·f 0 CH3H3C 405 e 5, \:Vhite Foam Step 2 ation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 406 Example 5, White Foam Step 2 407 Example.:\ White Foam Step 2 408 Example 5, \:Vhite Foam Step 2 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Prepared *Cmpd. ing Structure Appearance No. To Example 409 H3C,oc; Example 5, White Foam 0 F Step 2 ?''•·(o0 0 CH3 0 O 'CH3 H3C,... 410 oc; ,.,...CH3 ,.,...CH3 Example 5, White Foam 0 0 Step 2 ?'-(,. 0 0 CH3 ,...0 411 oc; ,.,...CH3 Example 5, White Foam 0 Step 2 ?''·(o0 0 CH3 H3C,...
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According ure Appearance No. To Example 412 .,...CH3 .,...CH3 Example 5, Oil 0 0 Step 2 ?''•? 0 CH3H3C 413 H3C, Example.:\ White Foam 0 F Step 2. ?''•? 0 CH3 ,..,O 414 H3C...._ Example 5, Thick Oil 0 CH3 Step 2. «?'-?0 0 CH3H3C [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 415 Example 5, White Foam Step 2. 416 Example 5, White Foam Step 2. 417 Example 5, White Foam Step 2.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Prepared *Cmpd. According Structure ance No. To Example 418 Example 5, White Foam Step 2. 419 Example 5, White Foam Step 2.
F F 420 Example 5, Colorless Step 2. Foam [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 421 H3C, H3C, e 5, Clear, 0 0 6=; Step 2. Colorless Oil H,,r'· 0 ,,.CH3 0 0 0 CH3 H3C, ,,.CH3 0 0 422 H3C, Example 5, Clear, 0 CH3 Step 2. Colorless Oil H,,.f o ,,.CH3 0 CH3 ,,.CH3 H3C 0 423 H3C,6=; Example 5, Colorless 0 Step 2. Foam H,,r'· 0 ,,.CH3 0 0 0 CH3 [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 424 Example 5, Colorless Step 2. Foam 42:'i Example 5, Cleac Step 2. Colorless Oil 426 Example 5, Clear, Step 2. Colorless Oil ation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 427 Example 5, Clear, Step 2. Colorless Oil 428 Example 5, White Foam Step 2. 42lJ Example .:\ Stich Wax Step 2.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example 430 Example 5, Colorless Gel Step 2 431 Example 5, Colorless Gel Step 2 .,,,,y ? 432 Example 5, Colorless Gel Step 2 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by an Prepared *Cmpd.
Structure According Appearance No. To Example 433 Example 5, Colorless Gel Step 2 43--l- Example .:\ Colorless Oil Step 2 CH3 ? .. ,,,y 435 H3C, Example 5, Colorless Oil 0 Step 2 0 CH3 ?,, Jl .••''Y? '·( 'o 0 CH3 CH3 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 436 e 5, Colorless Oil Step 2 437 e .:\ Colorless Oil Step 2 438 Example 5, Colorless Step 2 Foam .,,,,yr)' [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To 439 Example 5, Colorless Step 2 Foam CH3 ? .. ,,,y 440 Example .:\ Colorless Oil Step 2 441 Example 5, Colorless Oil Step 2 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According ure Appearance No. To Example 442 Example 5, White Foam Step 2 443 Example 5, White Foam Step 2. .,,,,y ? 444 Example 5, White Foam Step 2.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 445 Example 5, White Foam Step 2.
CH3 ? ..,,,y 446 Example 5, White Foam Step 2. 447 Example 5, \:Vhite Foam Step 2 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example 448 Example 5, White Foam Step 2 4lJ Example.:\ White Foam Step 2 450 Example 5, White Foam Step 2 [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 451 Example 5, White Foam Step 2 45.2 Example 5, Colorless Oil Step 2 453 Example 5, Colorless Oil Step 2 ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 454 Example 5, White Foam Step 2. 455 Example 5, White Foam Step 2. 456 Example 5, White Foam Step 2.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According ure Appearance No. To Example 457 Example 5, White Foam Step 2. 458 Example 5, White Foam Step 2. 459 Example 5, \:Vhite Foam Step 2.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To 460 Example 5, White Foam Step 2. 461 Example.:\ White Foam Step 2. 462 Example 6B. Slightly Opaque Colorless Viscous Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example 463 e 6B. Slightly Opaque Colorless Viscous Oil 464 Example 6B. Yellow Oil 465 Example 6B. Clear, Colorless Oil ation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 466 Example 6B. Pale Yello\\ 467 Example 6B. Pale Yello\\ 468 H3c, 0YCH3 Example 6A. Fluffy White N6 ?,.0 Powder ?N? 'f1 'O 0 CH3H3C [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example 469 Example 6A. Clear, Colorless Oil 470 H3c...__ o1cH3 Example 6A. Cleac O Colorless Oil t'( Jl0 'o 0 CH3 471 Example 6A. Clear, Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd.
Structure According Appearance No. To Example 472 Example 6B. White Foam 473 O CH3 e 6B. Sticky Wax H3C, (0 0 F F 47--l- O CH3 Example 6B. Colorless Oil H3C, (0 ? CH3 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example 475 Example 6A. White Foam 476 Example 6B. White Foam 477 Example 6A. White Foam ation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 478 Example 6A. White Foam F F 479 Example 6A. \:Vhite Foam 480 Example 6B. White Foam [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 481 Example 6B. White Foam 482 O CH3 Example 6B. White Foam H3C ....._ (0 0 CH3 0 483 O CH3 Example 6B. White Foam H3C, (0 « Cl 0 ?0CH3 0 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd.
Structure According Appearance No. To Example 484 Example 6B. White Foam 485 H 3 c, 0 3 Example 6A Colorless Oil ?b 0 CH ?N? '(1'O 486 e 6A Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 487 Example 6B Colorless Oil 488 Example 6A. e Foam 489 Example 6A. \Vhitc Foam [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 490 Example 6A. \\bite Wax 491 Example 6A. White Foam 492 Example 6A. White Foam [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 493 e 6B White Foam 49..J. Example 6C \:Vhitc Foam 495 Example 6A White Foam [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan 1002377274 *Cmpd. Structure Prepared Appearance No. According to Example 496 e 6A White Foam 497 H3C O CH3 Example 6A ess O Film O CH3 N CH3 N O O O CH3H3C CH3 498 Example 6A. White Foam ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example 499 Example 6A. White Foam 500 Example 6A. \:Vhite Foam 501 Example 6A. White Foam 502 Example 6A. White Foam [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 503 Example 6A. White Foam 504 Example 6A. White Foam F F 505 e 6A. Clear, Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure ance No. To Example 506 H3c, 0 CH3 Example 6A. Clear, Y Colorless Oil ? ?,, ?N>y 'f1'O 0 CH3 507 Example 6A. Clear, Colorless Oil 508 Example 6A. Clear, Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan *Cmpd. According Structure Appearance No. To Example 509 Example 6A. Clear, Colorless Oil 510 Example 6A. Cleac Colorless Oil 511 Example 6A. Clear, Colorless Oil [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To 512 Example 6A. Clear, Colorless Oil 513 Example 6B. Clear, Colorless Oil 514 Example 6B. Clear.
Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 515 Example 6B. Clear, Colorless Oil 516 Example 6B. Clcac Colorless Oil 517 e 6B. Clear, Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 518 Example 6B. Clear, ess Oil 519 Example 6B. Clear, Colorless Oil 520 Example 6B. Clear.
Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure ing Appearance No. To Example 521 Example 6A. White Foam. 522 Example 6A. Stich White 523 Example 6A Colorless Oil ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 524 Example 6A ess Oil 525 Example 6A Colorless Oil 526 Example 6A Colorless Oil [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 527 Example 6A Colorless CH3 ? ..,,,y Example 6A Colorless CH3 ? ..,,,y 529 Example 6A Colorless [Annotation] an None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 530 Example 6A Colorless 531 Example 6A Colorless Oil 532 Example 6A Colorless Oil ..,,,yrY [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by an Prepared *Cmpd. According Structure Appearance No. To Example 533 Example 6A Colorless Oil 53--l- Example 6A Colorless Oil 535 Example 6A. \:Vhite Foam [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd.
Structure According Appearance No. To Example 536 Example 6A. White Foam CH3 ? ..,,,y S-37 Example 6A. White Foam 538 Example 6A. \:Vhite Foam CH3 ? __,,,y [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure Appearance No. To Example 539 Example 6A. White Foam 540 Example 6A. White Foam 541 Example 6A. White Foam [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. ing Structure ance No. To Example 542 H30\OH3CYO Example 6A. White Foam l H \ N N , 543 Example 6A. White Foam Example 6A. White Foam [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared *Cmpd. According Structure ance No. To Example 545 Example 6A. White Foam 546 Example 6A. White Foam 547 Example 6A White Foam ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared * C132)pd. .
Structure Achcligdmg Appearance Example 548 H3C\O OYCHS Example 6A. White Foam / o I H \ N,, N " O 0 CH3 549 H3,C\O OYCHB e 6A. White Foam O CH 3 / 0 CH3 l H \ N h ‘\\\ N O ‘ 0 CH3 U1 ‘Ji 0 I 03O O OI w Example 6A. White Foam O o_/< [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared * Cmpd. According Structure ance No. To Example 55 l H3C \ Example 6A. White Foam 552 HSC \ Example 6A. White Foam UI Ul U) Example 6A Colorless [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Prepared * Cmpd. According Structure ance No. To Example 554 H C\3 O CH Colorless 3 e 6A O Y Foam / O \ N,, N " O 0 CH3 >“Cmpd. No. — Compound Number [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Table 2. ical Data Cmpd. MP IR NMR No. (CC) (c1111) (‘H, ”C, 19F) ‘H NMR (500 MHz. CDCL.) 5 7.53 4 7.41 (m, 4H), 7.32 4 7.23 (m. 4H), 7.23 4 HRMS—ESI 7.13 (m, 2H), 6.01 (q, J: 6.3 Hz, 1H), (m z) 4.98 (d. .1: 8.0 Hz. 1H). 4.13 (p. .1: 7.1 My Hz. 1H). 2.78 (s. 1H). 1.41 (s. 9H). 1.21 calcd for (d, J: 6.3 Hz, 3H). 0.53 (d, J: 7.3 Hz.
C23H29N05, 3H) 399.2046; found, ”C NMR (126 MHz, CDC13)5 172.55, 48 154.95,145.04.142.56, 128.32, 125.30. 127.17.127.11.125.59. 125.52.79.83. 79.54. 75.16. 49.13. 28.29. 17.95. 14.38 1H NMR (400 MHz, CDC13) 5 7.42 — 7.07 (m, 10H), 5.80 (dq,J= 10.1, 6.1 Hz, 1H). 4.97 (d. .1: 8.0 Hz. 1H). 4.19 4 4.06 (m, 1H), 4.03 (5,1: 101 Hz. 1H), 1.41 ESIMS (s, 9H), 1.23 (d, J: 6.1 Hz. 3H), 0.76 (d, 2 m z 3845 .1: 7.2 Hz. 3H) (1M+HJ+) 13C NMR (101 MHz, CDC13) 5 172.83. 154.96,141.52,141.26, 128.79, 128.50. 128.10. 128.08. 126.91. 126.67. 73.10. 57.98. 28.33, 19.31.1798 1H NMR (400 MHz, CDClg) 5 7.22 — 7. 15 (m. 2H). 7.00 (ddd. .1: 3.5. 1.2. 0.6 Hz. 1H). 6.97 4 6.89 (m. 3H). 5.52 (dq, .1 = 7.3. 6.2 Hz, 1H). 4.99 (d, J: 5.1 Hz.
ESIMS 1H). 4.63 (d. J: 7.3 Hz. 1H), 4.29 — 4.18 m z 396.5 . (m. 1H). 1.43 (s. 9H). 1.28 (d. .1: 6.2 Hz. 3 " ([M4Hr) 3H). 1.04 (d, J: 7.2 Hz, 3H) 13C NMR (101 MHz. CDC1~.) 5 172.64. 143.87. 142.87, 126.75. 126.55. . 125.39. 124.58. 124.56, 79.69. 74.40, 4931.47.46, 28.32, 15.74. 18.22 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 5 7.31 4 7.16 (m, 4H), 6.97 (td, J: 8.7, 7.0 Hz, 4H), 5.71 (dq, .1: 9.8. 6.1 Hz, 1H). 4.95 ESIMS (d, J : 8.0 Hz, 1H), 4.22 4 4,07 (m, 1H), m/Z 420.6 4.03 (d, J: 9.8 Hz, 1H), 1.42 (s, 9H), ([M+H]+) 1.22 (d, .1: 6.2 Hz, 3H). 0.84 (d. .1: 7.2 Hz, 3H) 19F NMR (376 MHz, CDC13) 5 411594 1H NMR (400 MHz, CDC13) 5 7.37 4 7.19 (m, 10H), 6.01 4 5.89 (m, 1H), 5.02 ESIMS (d, .1: 7.9 Hz, 1H), 4.27 4 4.10 (m. 1H), m z 450.6 3.38 (dq. .1 : 8.96.9 Hz, 1H), 3.25 4 ([M+Na]+) 3.13 (m, 1H), 1.40 (d, J: 2.1 Hz, 9H), 1.18 (t, J: 7.0 Hz, 3H), 1.15 4 1.06 (m, 1H NMR (400 MHz, CDC13) 5 7.38 4 ESIMS 7.21 (m, 10H), 6.01 4 5.82 (m, 1H), 5.01 6 m z 4366 (d, .1: 8.0 Hz, 1H), 4.27 4 4.12 (m. 1H), (1M4Nar) 3.15 (s, 3H). 1.40 (s. 9H), 1.15 4 1.07 (m, 1H NMR (400 MHz, CDC13) 5 7.36 (td, J : 8.5, 6.1 Hz, 1H), 7.26 4 7.15 (m. 1H), 6,914 6.68 (m, 4H), 5.86 4 5.73 (m, 1H), 4.92 (d,J= 8.0 Hz, 1H), 4.66 (d, J: 10.1 [52521655, Hz, 1H). 4.23 4 4.09 (m, 1H), 1.42 (s, 7 9H), 1.27 (d, .14 6.1 Hz, 3H) 19F NMR (376 MHz, CDC13)5 41 1 1.06 (d_ .1: 7.6 Hz), 41 1 1.55 (51.1: 75 Hz), 411 1,91 (dd, J: 7,9, 2.7 Hz), 4 112.72 (d, J: 5.9 Hz) 1H NMR (400 MHz. CDCL.) 5 7.48 4 7.41 (m. 4H), 7.38 4 7.19 (m, 6H). 5.97 (dq, J: 25.6, 6.5 Hz, 1H), 4.90 (d, J: ESIMS 7.8 Hz, 1H), 4.23 4 4.05 (m, 1H), 1.41 (s, 8 m z 424.5 9H), 1.29 (dd, .1: 6.5. 1.0 Hz, 3H). 0.75 ([M4Nar) (d, J : 7.2 Hz, 3H) ”P NMR (376 MHz. CDCL) 5 4169.03 [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NIVIR N0. (‘0 (cm'l) (1H, 13C. 191:) 1H NMR (400 MHz. CDC13) 5 7.22 4 7.09 (m. 4H). 6.91 4 6.65 (m. 4H). 5.70 (dq. .1: 9.8. 6.1 Hz. 1H). 4.94 (d. .1: 8.0 Hz. 1H). 4.19 4 4.05 (m. 1H). 3.93 (d.J: ESIMS 9.8 Hz. 1H). 3.76 (s. 3H). 3.74 (s. 3H). m 2 444.6 1.42 (s. 9H). 1.21 (d. .1: 6.2 Hz. 3H).
(| M+H 1+) 0.83 (d. .1: 7.2 Hz. 3H) ”C NMR (101 MHz. CDC13) 5 172.84. 158.34. 158.22. 133.99. 133.81. 128.96. . 113.84. 79.64. 73.33. 56.17. 55.22. 49.22. 28.31. 19.28. 18.19 1H NMR (400 MHz. CDC1~,) 5 7.33 4 7.21 (m. 2H). 7.14 4 7.02 (111.2H). 7.03 4 6.84 (m. 4H). 5.72 (dq. J: 2 Hz.
ESIMS 1H). 4.93 (d. .1: 8.0 Hz. 1H). 4.22 4 4.07 m 2 420.6 (m. 1H). 4.03 (d. .1: 9.8 Hz. 1H). 1.42 (s.
(UVHHY) 9H). 1.24 (d. J: 6.2 Hz. 3H). 0.84 (d. J: 7.1 Hz. 3H) ”P NMR (376 MHz. CDCL.) 5 -112.14. -112.59 1H NMR (400 MHz. CDC13) 5 7.33 4 7.11 (m. 8H). 5.71 (dq. .1: 10.0. 5.9 Hz. 1H). 4.94 (d. J: 8.0 Hz. 1H). 4.18 4 4.07 (m. 1H). 3.99 (d, J: 9.9 Hz. 1H). 1.42 ESIMS (d. .1: 1.7 Hz. 9H). 1.24 (d. J: 6.2 Hz. m Z 452.5 3H). 0.87 4 0.81 (111.3H) ([M+H]+) ”C NMR (101 MHz. CDC13) 5 172.79. 154.94. 142.68. 142.43. 134.73. 134.43. 130.21.129.93.128.39. . 127.49. 127.18. 126.28. 126.20. 79.79. 72.40. 57.09. 49.15. 28.30. 19.21.18.04 1H NMR (400 MHz. CD0.) 5 7.79 4 7.72 (m. 2H). 7.72 4 7.62 (m. 1H). 7.59 4 ESIMS 7.48 (m. 1H). 7.46 4 7.36 (m. 2H). 7.36 4 m 2 382.5 12 7.25 (m. 2H). 5.81 4 5.64 (m. 1H). 5.09 ([M+H1+) (s. 1H). 4.55 4 4.34 (m. 1H). 4.33 4 4.18 (m. 1H). 1.46 (s. 9H). 1.45 (d. J: 3.5 Hz. 3H). 0.70 (d. .1: 6.3 Hz. 3H) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. ”C. 191:) 1H NMR (400 MHz, CDC13) 5 7.33 4 ESIMS 7.21 (m, 4H), 7.15 4 7.04 (m, 4H), 5.15 4 m z 398.6 5.03 (m. 1H). 5.01 (d. .1: 8.0 Hz. 1H).
([M4Hr) 4.35 4 4.24 (m, 1H), 4.27 4 4.15 (m, 1H). 1.44 (s, 9H), 1.29 (d, J: 7.2 Hz, 3H), 1.03 (d. .1: 6.4 Hz. 3H) 1H NMR (400 MHz. CDCL.) 5 7.46 4 ESIMS 7.36 (m, 4H). 7.17 4 7.07 (m, 4H), 5.71 m z 5425 (dq, J: 9.7, 6.2 Hz, 1H), 4.91 (d, J: 7.9 (|M+Hr) Hz. 1H). 4.13 (p. .1: 7.2 Hz. 1H). 3.97 (d, J : 9.8 Hz, 1H). 1.42 (s, 9H), 1.22 (d, J: 6.1 Hz, 3H), 0.86 (d, J: 7.2 Hz, 3H) 1H NMR (400 MHz. CDC];) 5 6.73 (d. J : 3.4 Hz. 1H). 6.67 (d. .1: 3.4 Hz. 1H).
ESIMS 6.59 4 6.46 (m, 2H), 5.43 (dq, J: 7.4, 6.2 m z 4245 Hz, 1H), 5.03 (d, J: 8.1 Hz, 1H), 4.42 (|M+Hr) (d. .1: 7.3 Hz. 1H). 4.24 (p. .1: 7.1. 6.7 Hz, 1H), 2.41 (5,1: 1.1 Hz, 3H), 2.40 (d,J= 1.1 Hz, 3H), 1.43 (s, 9H), 1.27 (d, .1: 6.2 Hz. 3H). 1.09 (d. .1: 7.1 Hz. 3H) 1H NMR (400 MHz. CDCL.) 5 7.18 4 ESIMS (11:, 4H). 7.11 4 7.02 (m, 4H), 5.75 (dq.J— 10.2, 6.2 Hz, 1H). 4.95 (d, J— 16 ”1511346 8.0 Hz. 1H). 4.1 1 (p. .1 : 7.4. 6.5 Hz. 1H). (1 J ) 3.95 (d,J: 10.0 Hz, 1H), 2.27 (s, 3H), 2.25 (s, 3H), 1.41 (s, 9H), 1.22 (d, J: 6.1 Hz. 3H). 0.80 (d. J: 7.2 Hz. 3H) 1H NMR (400 MHz. CDCL.) 5 7.55 (d, .1 = 8.1 Hz, 2H), 7.41 (d, J: 8.0 Hz, 2H), 7.314 7.16 (m. 5H), 5.82 (dq.J= 9.9.6.2 7773334154286 Hz. 1H). 4.92 (d. .1: 7.9 Hz. 1H). 4.15 4 18 4.06 (m, 2H), 1.41 (s, 9H), 1.24 (d, J4 ([M+H]+) 6.2 Hz, 3H), 0.77 (d, J: 7.2 Hz, 3H) ”P NMR (376 MHz. CDC];) 5 -62.58 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NIVIR N0. (‘0 (cm'l) (1H, 13C. 191:) 1H NMR (400 MHz, CDClg) 8 7.30 4 7.22 (m, 4H), 7.22 4 7.15 (m, 4H), 5.71 (dq, .1: 9.6, 6.2 Hz, 1H), 4.91 (d, .1: 8.0 Hz, 1H),4.214 4.06 (m, 1H), 4.00 (d, J: ESIMS 9.8 Hz, 1H), 1.42 (s, 9H), 1.22 (d, J: 6.2 m 2 4525 19 Hz, 3H), 0.85 (d, J: 7.2 Hz, 3H) (| M+H r) 13C NMR (101 MHz, CDC13) 8 172.75, 154.96, 139.41, 139.25, 133.03, 132.77, 129.43, 129.35, 129.05, 128747981, 7251, 56.45, 49.17, 28.30, 1918,1809 1H NMR (400 MHz, CDClg) 8 7.25 4 7,14 (m, 4H), 7.06 4 6,87 (111,4H), 5,68 (dq, .1: 9.3, 6.2 Hz. 1H), 4.83 (s, 1H), 4.02 (d, J: 93 Hz, 1H), 3.82 (dd, J: 18.2, 5.9 Hz, 1H), 3.56 (dd,J= 18.2, 5.2 ESIMS Hz, 1H), 1.43 (s, 9H), 1.22 (d, .1: 6.2 Hz, m 2 406,5 3H) 13C NMR (101 MHz, CDC1~,) 8 16966, 161.74 (d, .1:245.9 Hz), 161.63 ((1.1: 245.7 Hz), 155.45, 136.74, 129.65 (d,J= 7.9 Hz), 115.70 (d,J= 21.3 Hz), 11541 (d, .1: 21.2 Hz), 79.97, 77.21, 73.15, 5584, 42.44, 28.29, 19.17 1H NMR (400 MHz, CDClg) 8 7.30 4 7,15 (m, 4H), 7.06 4 6,89 (m, 4H), 5,75 4 .62 (m, 1H), 4.90 (d, .1: 8.4 Hz, 1H), 4.11 (q, J: 67 Hz, 1H), 4.03 (d, J: 9.8 ESIMS Hz, 1H), 1.494 1.33 (m, 10H),1.30— m 2 434.6 1.08 (m, 4H), 0.54 (t, .1: 7.4 Hz, 3H) 13CNMR (101 MHz, CDC13) 8 172.10, 161.70 (d, .1: 245.6 Hz), 155.20, 136.97, 129.52, 115.7l(d,.1:21.3 Hz), 115.44 (d,J= 21.2 Hz), 79.73, 73.12, 56.08, 54.46, 28.30, 25.40, 19.26, 8.95 ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR Nh/IR N0. (‘0 (cm'l) (1H, 13C. 191:) 1H NMR (400 MHz, CDC13) 5 7.30 4 7.15 (m, 4H), 7.04 4 6.91 (m, 4H), 5.69 (dq. .1: 9.7.6.1 Hz. 1H). 4.86 (d. .1: 9.3 Hz, 1H), 4.09 (dd, J : 9.3, 4.2 Hz, 1H), 4.03 (d, J: 9.8 Hz, 1H), 1.69 4 1.57 (m, 1H). 1.42 (s. 9H). 1.21 (d. .l:6.2 Hz.
ESIMS 3H). 0.73 (d. .1: 6.9 Hz. 3H). 0.43 (d. .1: m 2 448.6 22 6.8 Hz, 3H) ([M—1—H]+) ”C NMR (101 MHz. CD(‘,1~,)5 171.77. 161.73 (d,J: 246.0 Hz), 155.60, 137.05, 129.61,129.52,129.44,115.71(d,J= 21.6 Hz). 11549 (d. .1: 21.4 Hz). 7969. 73.23. 58.49. 56.03. 30.92. 28.28. 19.31. 18.96, 16.54 1H NMR (400 MHz, CDC13) 5 7.30 4 7.20 (m. 4H). 7.04 4 6.92 H). 5.68 (dq, .1: 9.8, 6.2 Hz, 1H), 4.72 (d, J: 8.9 Hz, 10 (td,J= 9.2, 5.1 Hz, 1H), 4.02 (d. .1: 10.0 Hz. 1H). 1.41 (s. 9H). 1.22 (d. .1: 6.1 Hz. 3H). 0.96 (ddd. .1: ESIMS 13.7, 9.6, 5.5 Hz, 1H), 0.84 (m, 1H). 0.75 m 2 462.7 (d, J: 6.5 Hz, 3H), 0.70 (d, J: 6.6 Hz, (| M+H |+) 3H) ”C NMR (101 MHz, CDC13) 5 173.06, 161.72 (5.1: 245.8 Hz). 155.29. 137.17. 136.83. 129.49. 115.73 (d../: 21.4 Hz). 115.46 (d, J: 21.3 Hz), 79.74, 73.02, 56.27, 52.04, 41.48, 28.28, 24.41, 22.76, 21.53. 19.23 (Thin ?lm) HRMS-ESI 1H NMR (300 MHz, CDC13)8 7.50 4 3358. (m z) 7.37 (m. 1H). 7.29 4 7.19 (m. 1H). 7.20 4 2977. |M+Nar 7.06 (m. 2H). 6.92 4 6.75 (m. 4H). 5.91 1708 calcd for (dq,J= 10.1.6.4 Hz, 1H), 5.03 4 4.97 1491, C25H33NN€1064 (m, 1H), 4.98 (d, J: 9.9 Hz, 1H), 4.22 4 1243. 466.22; 4.04 (m. 1H). 3.84 (s. 3H). 3.76 (s. 3H). 1162, found, 1.41 (s, 9H), 1.23 (d, J : 6.2 Hz, 3H), 1051, 466.2191 0.82 (d,J= 7.2 Hz, 3H) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) (Thin 1H NMR (300 MHz, CDClg) 5 7.18 (dt, J ?lm) 111137178581 = 11.8, 7.9 Hz, 2H), 6.89 (dq, J: 7.6, 1.5 3368. Hz. 2H). 6.83 (dt. J: 4.0, 2.1 Hz. 2H).
| M+Nal+ 2978, 6.71 (dddd, J: 10.7, 8.2, 2.6, 0.9 Hz, calcd for 1707, 2H), 5.77 (dq, J: 10.2, 6.1 Hz, 1H), 4.96 OH «NNaO 1597. 3456 22, 6’ (d. .1: 8.0 Hz, 1H). 4.20 4 4.01 (m. 1H), 1488. fou11d‘ 3.96 (d. .1: 10.3 Hz. 1H). 3.77 (s. 3H). 1156, 3.75 (s, 3H), 1.42 (s, 9H), 1.24 (d,J= 6.2 466 2193 1043 ' Hz, 3H), 0.79 (d, J: 7.2 Hz, 3H) (Thin 38! 1H NMR (300 MHz. CDCL.) 5 7.14 4 7.02 (m, 2H), 6.99 4 6.84 (m, 4H), 5.67 ?lm) 3368 ([M+H]+) (dq, J: 9.8, 6.2 Hz, 1H), 4.95 (d, J: 7.9 ‘ mlcd‘ Hz, 1H). 4.22 4 4.05 (m, 1H). 3.94 (d. .1: 26 I?” “?led for 9.8 Hz. 1H). 2.20 (d. J : 2.1 Hz. 3H). ?g; C25§;6F§T1§?O4= 2.19 (d, J: 2.2 Hz, 3H), 1.42 (s, 9H), ' ‘ 1.284 1.17 (m, 3H). 0.86 ((1.1: 7.2 Hz. 1032 found, 470.2122 ‘3 H) (Thin 1111371782331 1H NMR (300 MHz, CDC13) 5 7.22 (dd, J : 4.6, 1.9 Hz, 2H). 7. 13 (t, .1: 7.9 Hz. ?lm) (1M+HJ+) 2H), 7.04 (ddd,J: 7.6, 5.1, 1.9 Hz, 2H), 3366 calcd 27 2978’ 5.67 (dq, J: 10.0, 6.2 Hz, 1H), 4.96 (d,J calcd for 1706 : 7.9 Hz. 1H). 4.22 4 4.05 (m, 1H). 3.91 (,er CleNaO4‘ “62‘ ’5‘ 562 1,22, (5.1: 9.9 Hz, 1H), 2.31 (s, 3H). 2.29 (s, 1051’ fo1u1d * 3H), 1.42 (s, 9H), 1.22 (52.1: 6.0 Hz, 33 3H), 0.87 (d,J= 7.2 Hz, 3H) (1:11;; ”1127475231381 1H NMR (300 MHz, CDCl;) 5 7.45 4 7.37 (m, 4H), 7.26 4 7.18 (m, 4H), 5.75 3285 [M+Na]+ 2979’ (dq. J: 10.0, 6.1 Hz. 1H). 4.91 (d. .1: (?led for 28 2107‘ 7.9 Hz, 1H). 4.20 4 4.06 (m, 1H). 4.04 (d, C) H“ NNaO 1702’ {5:989 4’ J: 9.9 Hz, 1H), 3.05 (s, 1H), 3.04 (s, 1501’ d 3 1H) 1.42 (s, 9H), 123 (5:1: 6.2 Hz, 3H). 0.82 (d. .14 7.2 Hz, 3H) 1160 4541993 (Thin HRMS—ESI 1H NMR (300 MHz, CDC13) 5 7.22 4 ?lm) (777 z) 7.16 (m, 4H). 7.13 4 7.03 (m, 4H), 5.76 3362. |M+Nar (dq. .1: 10.2, 6.1 Hz. 1H). 4.95 (d. .1: 2964, calcd for 7.8 Hz, 1H), 4.17 4 4.02 (m, 1H), 3.96 (d, 1712, C27H3-NNaO4, J: 10.2 Hz, 1H), 2.67 4 2.45 (m, 4H), 1510. 4622615; 1.41 (s, 9H). 1.23 (d. .1: 6.2 Hz. 3H). 1163. found, 121 4 1,10 (m, 6H). 0.73 (d. .1: 7.2 Hz. 1053 462.2622 3H) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR MASS NMR N0. (‘0 (cm'l) (1H. 13C. 191:) 1H NMR (400 MHz. CDC13) 5 7.32 — 7.20 (m. 6H). 7.20 — 7.14 (m. 1H). 6.97 (1. .1: 8.7 Hz. 2H). 5.75 (dq. .1: 10.0.6.2 Hz. 1H). 4.92 (61.1: 8.0 Hz. 1H).4.11(t.
J: 7.4 Hz. 1H). 4.02 (d. J: 10.0 Hz.
ESIMS 1H). 1.41 (s. 9H). 1.23 (d. .l:6.2 Hz. m Z 402.6 3H). 0.77 (d. .1: 7.2 Hz. 3H) ([M+H]+) ”C NMR (126 MHz. CDC13) 5 172.81. 161.71 (d. .1:245.7 Hz). . 141.23. 137.03 (d. J: 3.5 Hz). 129.56 (d. J: 7.9 Hz). 128.59. 127.99. 126.82.115.62(d.J : 21.3 Hz). 79.70. 72.94. 57.09. 49.16. 28.31. 14.13 1H NMR (400 MHz. CDC13) 5 7.58 (t. J = 2.1 Hz. 2H). 7.38 (dd. J: 8.4.3.9 Hz. 2H). 7.29 4 7.25 (m. 1H). 7.20 (dd. .1: 8.5. 2.2 Hz. 1H). 5.84 (q. J : 6.2 Hz. 1H). 4.94 (d. J: 7.8 Hz. 1H). 4.14 (t. J: 7.4 Hz. 1H).3.05 (s. 1H). 1.41 (s. 9H). 1.18 ESIMS (d. .1: 6.3 Hz. 3H). 1.00 (d. .1: 7.2 Hz.
DJ U) 96 (1M-H201+) 3H) ”C NMR (126 MHz. CD(‘,1~.)5 172.37. 155.04. 144.43. 142.16. 132.90 (d.J: 2.7 Hz). 131.93. 131.87. 130.51. 130.46. . 127.70. 125.08. 124.99.80.20. 78.55. 74.10. 49.16. 34.67. 28.25. 14.28 1H NMR (400 MHz. CDC13) 5 7.37 — 7.28 (m. 4H). 7.18 (ddd. J: 8.4. 2.2. 0.8 Hz. 1H). 7.09 (ddd. J: 8.4.2.209 Hz. 1H). 5.86 (q. J: 6.2 Hz. 1H). 4.93 (d. J: 7.8 Hz. 1H). 4.14 (t. J: 7.4 Hz. 1H). 3.06 (s. 1H). 1.41 (s. 9H). 1.18(d..1:6.3 Hz. 3H). 0.98 (d. .1: 6.8 Hz. 3H) ESIMS m 2 486.5 ”C NMR (126 MHz. CDC13) 5 172.28.
(I M-HzOF) 158.09 (d. .1: 249.9 Hz). 158.06 (d. .1: 2495 Hz). 155.05.145.31(d..1: 5.7 Hz). 142.98. 130.64 (d. J: 10.0 Hz). 121.90 (d. .1: 8.8 Hz). 120.38 (d. .1: 12.3 Hz). 120.24 (d. .1: 12.3 Hz). 114.59 (d. J: 22.6 Hz). 114.20 (d. J: 22.9 Hz). 8019. 78.60. 74.13. 49.13. 34.67. 28.25. 14.30 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by an Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) 1H NMR (400 MHz, CDC13) 5 7.24 (dd, J = 10.4, 8.1 Hz, 2H), 7.09 (dd,J= 5.5, 2.2 Hz, 2H), 7.02 (td, J: 86,23 Hz, 2H), ,69 (dq,J: 10.1, 6.1 Hz, 1H), 4.94 (d,J = 7.9 Hz, 1H), 4.13 (t, J: 7.5 Hz, 1H), 3,92 (d, .1: 10.0 Hz, 1H), 2.33 (s, 3H), ESIMS 2.31 (s, 3H), 1.42 (s, 9H), 1.21 (d, .1: 6.1 m 2 4806 Hz, 3H), 0.84 (d, J: 7.2 Hz, 3H) ([MT) "C, NMR (126 MHz, CD(‘,1~,) 5 172.81, 154.92, 139.66, 139.44, 136.53, 136.10, 133.08,132.72,130.69, 130.57, 129.43, 129.12, , 126.46, 79.77, 7261, 5649,4917, 28.29, 20.16, 20.09, 19.23, 1H NMR (300 MHz, CDC13_) 5 7.82 (ddd, (Thin .1: 8.6, 7.3, 1.8 Hz, 1H), 7.51 (a, .1: 7.9, Hz, 1H), 73 4 7.12 (m, 3H), 7.09 2980, (td, J: 7.6, 1.4 Hz, 1H), 6.94 (dd, J: 36 1669’ 8,1, 1.4 Hz, 1H), 6.90 (dd, .1: 8.1, 14 1486‘ Hz, 1H), 6.23 (qd, .1 : 6.3, 1.6 Hz, 1H), ”52’ 5.02 (d, J: 79 Hz, 1H), 4.30 — 4.13 (m, 1H), 3.21 (s, 1H), 1.42 (s, 9H), 1.26 (d, J 1160 {,7 : 6.2 Hz, 3H), 1.07 (d, .1: 7.2 Hz, 3H) (Thin 3375, 2981, 1703, 1 , 1609 HNMR(500_MHz, CDC13)8 7.18 — 1515’ 6,9] (m, 6H), 5.63 (dq, .1: 9.4, 6.2 Hz, 1573‘ HRMS-ESI 1H), 4.92 (d, .1: 8.0 Hz, 1H),4,241 4 4.06 1433? (m z) (m, 1H), 3.98 (d,J= 9.5 Hz, 1H), 1.42 (s, 1380’ [M+Na] 9H), 1.23 (d, J: 6.1 Hz, 3H), 0.91 (d, J: calcd for 7.2 Hz, SH) ___ 1:367‘ 1284‘ C23H35F1NNaO1, 1250’ 478.1612; F N1V_IR (471 MHz, CDC13) 5 1208 found, 43625 (dt, .1: 20.6, 9.7 Hz), 4781624 43669 (dt, .1: 20.4, 9.9 Hz), 11 62‘ “13> -139.30(dd,J=21.3,10.5Hz), 105?; -139.70(dd,J=21.1,10,1Hz) 1023, 967, 909, 873, 821, 754, [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS.
N0. (0C) (cm'l) (H. 13C. 191:) (Thin 3440. 2981. 1704. 128(7) 1H NMR (300 MHz. CDC];) 5 7.32 4 1452‘ HRMS-ESI 7.22 (m. 2H). 7.18 4 7.02 (m. 4H). 5.64 13'79’ (m z) (dq. J: 9.6. 6.2 Hz. 1H). 4.93 (d. J: 8.0 1367, [M+Na] Hz. 1H). 4.25 4 4.03 (m. 1H). 3.98 (d. J: calcd for 9.6 Hz. 1H). 1.42 (s. 9H). 1.23 (d. .1: 6.2 ___ 1306‘ - C33H25C13F3NNaO4. Hz. 3H). 0.92 (d. J = 7.2 Hz. 3H) 1250. 510.1021; found. W F NMR (471 MHz. CDC];) 0a 1 162‘ _‘ 510.1033 -116.98(q.J:6,9 Hz).-117,44(q.J: 1095. 6 8 Hz) 1054. ' 1023. 907. 867. 822. 799. 780. 731. 719.
(Thin 3364. 2980. 2931. 1HNMR (300 MHz. CDC13) 5 7.13 —,, ,, ”97‘ 6.98 (m. 4H). 6.90 (td. .1: 9.1. 7.4 Hz. 1%01‘ HRMS-ESI 2H). 5.67 (dq. J: 10.1.6.1Hz. 1H). 4.93 14513 (m z) (d. J: 8.0 Hz. 1H). 4.22 — 4.02 (m. 1H). ”'79’ [M+Na] 3.91 (d. .1: 10.1 Hz. 1H). 2.23 (d. .1: 2.0 1366‘ calcd for Hz. 3H). 2.21 (d. J: 2.0 Hz. 3H). 1.42 (s. 39 ___ 1307’ F3NNaO4. 9H). 1.21 (d. J: 6.1 Hz. 3H). 0.83 (d. J: ’ 470.2113; 7.2 Hz. 3H) 1248.. found. 1 207 470.2120 w 1163‘ F NMR (471 MHz. CDC13) oA ’ -119.99 (q.J=6.8 Hz). -120.57 (q.J= 1118. 7 0 Hz) 1052. ‘ 1023. 959. 908. 881. 821. 781. ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 5 7.53 (ddd.
J: 13.6, 6.7, 4.2 Hz, 8H), 7.45 — 7.37 (m. 8H). 7.35 4 7.29 (m. 2H). 5.87 (dq../ : 12.3. 6.1 Hz. 1H), 4.94 (d,J: 7.1 Hz, 1H), 4.18 — 4.09 (m, 2H), 1.41 (s, 9H), ESIMS 1.31 (d. .1: 6.2 Hz. 3H). 0.80 (d. .1: 7.1 m z 536 Hz, 3H) 40 ___ ___ +) ”C NMR (126 MHz, CDC13) 5 172.93. 154.96. 140.72. 140.60. 140.56. 140.21. 139.92,139.68,128.76, 128.75, 128.51, 127.58,127.30,127.27, 127.23, 127.00, 126.96. 79.70. 73.12. 57.33. 49.22. 28.31. 19.39. 18.04 1H NMR (400 MHz, CDC13) 5 7.38 (1..) = 8.1 Hz, 2H), 7.32 (dd, J: 13.6, 2.1 Hz, 2H). 7. 10 (dd. .1: 8.4. 2.1 Hz. 1H). 7.07 HRMS-ESI (dd. J: 8.4.2.1Hz, 1H). 5.65 (dq, J: (m z) 9.5, 6.2 Hz, 1H), 4.93 (d, J: 7.9 Hz, 1H), [M+Na1+ 4.22 4 4.09 (m. 1H). 3.97 (d. J: 9.5 Hz. calcd for 1H). 1.42 (d. .1: 0.9 Hz. 9H). 1.24 (d. .1: C33H25C14NNaO4, 6.1 Hz. 3H), 0.93 (d, J: 7.2 Hz, 3H) 542.0430; found. ”C NMR (126 MHz. CD(‘,1~.)8 172.73. 542.0442 154.93,140.37,140.26, 133.10, 132.76, 131.66,131.34,130.97,130.67,130.23, 130.06. 127.34. . 79.92. 71.96. 55.79. 49.16. 28.29.1914. 18.11 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. 13C. 191:) 1H NMR (400 MHz, CDC13) 8 7.38 — 7.28 (m, 2H), 7.06 (dd, J: 10.0, 1.8 Hz, 1H). 7.04 4 6.94 (m. 3H). 5.66 (ddt. .1: 9.1, 6,9, 5.5 Hz, 1H), 4.92 (d,J: 8.0 Hz, 1H), 4.22 — 4.08 (m, 1H), 4.01 (d, J: 9.4 HRMS—ESI Hz. 1H). 1.42 (d. .1: 1.3 Hz. 9H), 1.24 (m z) (dd. .1 : 6.2. 1.3 Hz. 3H). 0.92 (d. .1: 7.2 [M41921]+ Hz, 3H) calcd for 44 ___ ___ i hFZNNdm. "C NMR (126 MHz. CD(‘,1~,)5 172.68. 510.1021; 158.17(d,J:250,1Hz),158,03(d,J: found, 250.1 Hz), 154.93, 141.08 (d, J: 6.1 510.1030 Hz). 140.95 (d..I:6.1Hz). 131.11. 130.80. 12451 (d. .1: 3.3 Hz). 124.36 (d.
J: 3.6 Hz), 120.08 (d, J: 17.6 Hz), 11978 (d, J: 17.6 Hz), 11648 (d, J: 16.8 Hz). 116.24. 79.92. 72.02, 56.07. 49.15,28.28,19.10,18.10 ESIMS m z 300 4i ___ ___ ___ ‘ (lM+HJ+) ESIMS m Z 284.3 (1M+H1+) ESIMS mwz 296.3 (119141110 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, 13C, 191:) (Thin 3395, 2885, 1741, 1603, 1508, HRMS-ESI 1H NMR (400 MHz, CD(713)5 8.55 (s, 1459, (m 2) 3H), 7.22 (dt, J: 9.0, 4.8 Hz, 4H), 6.98 1381, ([M+H]+) (q,J= 8.2 Hz, 4H), 5.71 (dq,J= 11.8, 1324, calcd 6.1 Hz, 1H), 4.05 (d, .1 : 9.8 Hz, 2H), 48 1224, calcd for 1.23 (d, J: 5.9 Hz, 3H), 1.13 (d, J: 6.7 1159, C18H30F3N02, Hz, 3H) 1137, 3201457; 1118, found, ”F NMR (376 MHz, CDC];) 5 1049, 7 -115.32,-115,70 1015, 955, 881, 826, 793, 779, 755, 746, 721, 693, ESIMS 49 ——— ——— m z 341 ,5 --- ([M+Naj+) ESIMS m z 3 14,6 SO ___ ___ ___ “ (lM+HJ+) ESIMS 777 Z 35644 51 ___ ___ ___ ([M+H] ) ESIMS m z 3024 19F NMR (376 MHz, CDCl3) 8 “52 ([M+H]+) -169.31 ESIMS m z 344,; i“) ___ ___ ___ ‘ ‘ (lM+HJ ) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR MASS NMR N0. (‘0 (cm'l) (1H. 13C. 191:) ESIMS 171 Z 3204 (| M+H r) ESIMS m z 352 .4 (lM+HJ+) ESIMS m Z 2824 ([M—s—H]+) ESIMS m Z 2984 ([M+H]+) ESIMS 117 Z 442.4 (UVHHY) ESIMS m Z 324.4 ([M—s—H]+) ESIMS mwz 312.3 ([M+H]+) ESIMS 172 Z 436 (| M+H |+) ESIMS m Z 3755 ([M+Na]+) ESIMS 64 m2 375 .5 ([M+Na]+) [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR MASS NMR N0. (‘0 (cm'l) (1H. 13C. 191:) ESIMS 171 Z 3445 (| M+H r) ESIMS m 2 344.5 (1M+HJ+) ESIMS 177 Z 3485 ([M+H]+) ESIMS m 2 38015 ([M+H]+) ESIMS m 2 332.5 (1M+HJ+) ESIMS m Z 340.5 ([M+H]+) (Thin HRMS-ESI ?lm) (m z) 2959, ( 1M+H1+) 1749. cralcd 71 1508, calcd for 1401, F2N02, 1229. 306. 1300; 1 159. found. 1055, 830 306.1298 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. 13C. 191:) (Thin 31:12) SI ’ 7. _‘ (m z) 2833. 1742/ ([M+H]+) 16013 calcd 72 ——— 1506 calcd for --- ‘ 1454~ ,, C19H22FZNOZ; 12'20’ 335.1646; found. 1 ”9’5 ‘ 335 1646 1136; ' 1046, 824 ($111? HRMS-ESI (”7 Z) 2966 1 1736, ([M+H] ) 1602, ”led 73 ——— ”07‘ calcd for --- 1&121> C20H24F2N02: 1158, 349.1803; found. 1 1720‘ 1046 8‘25 3491804 HRMS—ESI (/77 Z) 2959. 173 9/ 16033 calcd 74 ——— calcd for --- 1; 077‘ 1219‘ C21H26F2N02> 11583 363.1959; found. 1046" 212%1 122’ 363.1959 (Thin 3'1]? HRMS—ESI 7 ‘ (m 2) ([MH]+) 1740’ 1605, calcd 75 ——— ”079‘ calcd for --- 1:153) C18H21FNOZ: 122,; 302.1551; found. 1 1377 ‘ 302 15513 1116, ' 1049. 700 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd MP IR NLASS NMR 140. (‘0 (cnfb (1H. 13C. 191:) (11mm 33 3. 2941, 1743, 1467. 1385. E51848 1236, 0 1201. ([1V14—11]+) 1173. 1136, 1117, 1061. 1029,992. 824,755, 723,675 3361, 2942. 1742. 1582, ESIBIS 78 1486. n724040 1419. (I M 1') 1240, 1207, 1141. 1116. 1057,800 (T1?n 3218, f?thS-ESI 2980, (n72) 2945. ([84+TJTU 1742. cmcd 79 1522, calcd.?3r 1481. C20H24C12N02, 1245. 3801179; 1216, fbund, 1136, 3801181 1118. 1048. 758 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. 13C. 191:) ESIMS m 2 404.4 (| M+Hr) ESIMS m 2 336.5 <1M+HJ+> ESIMS m 2 408,5 ([M+H]+) (Thin 2881. 2193. 2130, 1H NMR (300 MHz, ol-d4) o 7.46,, - 1609, HRMS—ESI 7 7.30 (m, 2H). 7.28 7 7.14 (m, 4H). 5.84 1516‘ (m z) (dq, J: 10.1, 6.2 Hz. 1H), 4.24 (d. J: 1&57’ ([M+H]+) 10.1 Hz, 1H), 3.96 (q, J: 7.3 Hz, 1H), 14343 cralcd 3.31 (pd, J: 1.6, 0.5 Hz, 3H), 1.27 (d,J 84 : 6.1 Hz. 3H). —-— 13%;“; calcd for 1.02 (d. .1: 7.2 Hz. 3H) 1532555 C18H18F4N02, 12853 356.1268; F NMR (471 1\/H-Iz,methanol-d4) o -a 1208 found, 139.39 (ddd. .1: 19.8, 11.5. 7.5 Hz), 1118‘ 3561273 - 39.57 7 -139.84 (m). -142.33 7 -142.56 (111), -142.66 — -142.93 (In) 1049 966 906, 875. 821, 754, 710, 692, 681, 656 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, 13C, 191:) (Thin 3409, 2928, 2026, 1H NMR (300 MHz, methanol-d4) 5 7.54 1957, , (dt, J: 7.0, 2.7 Hz, 2H), 7.37 (ddt, .1: HRMS‘ESI 1743, 8.6, 4.3, 2.1 Hz, 2H), 7.21 (td, J: 8.8, 1597, “Sign 4.7 Hz, 2H), 5.93 — 5.75 (m, 1H), 4.24 (d, 1499, J: 10.1 Hz, 1H), 3.96 (q, J: 7.3 Hz, cr'11cd 1458, 1H), 3.31 (t, J: 1.7 Hz, 3H), 1.28 (d, .1: ___ cal‘cd for Egg, 6.1 Hz, 3H), 1.03 (d, J7 7.3 Hz, 3H) C18H18C13F2N02, ’ 388.0677; 1249‘,. found 1‘ 1208, )F NMR (471 MHz, methanol-d4) 5 388 0677 1118, ' -119.62—-119.72(m), -119.99— 1061, 917, -120.08 (111) 866, 822, 798, 780, 753, 718, 690, 663 (Thin 3374, 2928, 1742, 1596, 1H NMR (300 MHz, methanol-d4) 5 7.30 1501, HRMS-ESI 7 7.12 (m, 4H), 6.95 (td, .1: 8.9, 6.6 Hz, 1457, (m 2) 2H), 5.91 7 5.74 (m, 1H), 4.07 (d, .1: 1379, +) 104 Hz, 1H), 3.99 — 3.83 (1n, 1H), 330 1323, calcd (dtd, J: 3.3, 16, 0.6 Hz, 3H), 2.23 (t, J: 86 ——— 1233, calcd for 2.6 Hz, 6H), 1.25 (d, .1: 6.1 Hz. 3H), 1206, C30H24F3N02, 0‘94 (dd, J : 73, 0.7 Hz, 3H) 1118, 348.1770; 1052, found, 19F NMR (471 MHZ, methanol-d4) 5 1003, 956, 348.1771 -122.0() 7 -122.37 (In), -122.69 (11.1: 933, 886, 6.1, 2.9 Hz) 824, 780, 752, 721, 711, 690, 681, 671, 664, 655 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, 13C. 19F) (Thin 2879, 1746, 1587, (”7 Z) ‘ + (| M+H| ) 1317,_ calcd 87 --- 1395’ calcd for --- 1227’ CIXHIXChNOg, ‘ 6; 1194,,, found, _,,’ 4200090 1033, 1029, 871. 822, 747, 727, 669 (Thin 2858, 1747, 1580, HRMS-ESI 1486, (m z) 145 8, ([M+H]+) 1383, calcd 88 ——— 1368, calcd for --- 1278, C18H18C13F3N03, 1236, 3880677; 1206, found, 1119, 388.0688 1048, 970, 871, 824, 779, 761, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. ”C. 191:) 1H NMR (500 MHz, CDC13) 8 11.97 (d, J = 0.5 Hz, 1H). 8.33 (d, J: 8.1 Hz, 1H), 7.96 (d. J: 5.2 Hz. 1H). 7.47 (ddt. J: HRMS-ESI 8.5. 6.4. 1.3 Hz. 4H), 7.33 4 7.13 (m. (m 2) 5H), 6.89 4 6.81 (m. 1H). 6.03 (q, J: 6.3 [MT Hz. 1H). 4.62 4 4.49 (m. 1H). 3.93 (s. calcd for 3H). 2.74 (s. 1H). 1.23 (d. J : 6.3 Hz.
Cstz?Nzoé, 3H), 1.07 (d. J: 7.2 Hz. 3H) 450.1791; found. ”C NMR (126 MHz. CD(‘,1~.)8 171.30. 450.1794 168.61.155.37.148.71.144.85, 142.71, 140.44.130.29,128.33, 128.32. 127.22, 127.16.125.51.125.45. 109.44. 79.57. 75.54. 56.08. 47.85. 17.62. 14.32 1H NMR (400 MHz, CDC13) 8 12.10 (d, J = 0.6 Hz, 1H). 8.34 (d, J: 8.0 Hz, 1H), 7.98 (d. J: 5.2 Hz. 1H). 7.38 4 7.06 (m. “mi-ES] 1011). 6.86 (dd. J: 5.3. 0.7 Hz. 1H). 583 (dq,J= 10.1. 6.1 Hz, 1H). 4.52 (dq. J: ([M+H]+) 8.1. 7.2 Hz. 1H). 4.06 (d. .1: 10.2 Hz. 1H). 3.93 (s. 3H). 1.26 (d. J: 6.1 Hz. 90 “?ed for 3H) 0 97 (d J: 7 2 Hz 3H) C25H2‘N205, 3 5 " 5 " 11961202 ”C NMR (101 MHz. CD(‘,1~.)8 171.67. 43; 192*; 168.53.155.3414872,141,38, , *' “ 140.40.130.48,128.80, 128.50. 128.10, 128.03. 126.95. 126.70. 109.39. 73.57. 57.93. 56.07. 47.85. 19.24. 17.61 1H NMR (400 MHz, CDC13) 8 12.10 (d, J = 0.6 Hz, 1H). 8.41 (d, J: 8.0 Hz, 1H), 7.98 (d. J: 5.2 Hz. 1H). 7.18 4 7.16 (m. “mi-ES] 2H). 7.01 (ddd. J: 3.6, 1.3. 0.6 Hz. 1H). 6.94 4 6.88 (m, 3H). 6.86 (dd. J: 5.3. 0.7 ([M+H]+) Hz. 1H). 5.56 (dq. J: 7.4. 6.2 Hz. 1H). calcd 4.70 4 4,58 (m. 2H). 3.94 (s. 3H). 1.30 (d. 91 calcd for J4 6.2 Hz, 3H), 1.24 (d. J4 7.2 Hz. 3H) C21H23N20582, 4:233:8‘ ”C NMR_(_101_ MHz. CDCE.) 8 171.48. 168.62.155.33.148.74, , 142.69, 447.1047 140.43. 130.48, 126.77, 126.57, 126.05, 125.43. . 124.58. 109.44. 74.83. 56.08. 47.98. 47.42. 18.69. 17.80 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDClg) 5 12.06 (d, J HRMS—ESI = 0.7 Hz, 1H), 8.32 (d, J: 8.0 Hz, 1H), (m z) 7.98 (d. J: 5.3 Hz. 1H). 7.26 4 7.18 (m.
([M+HJ+) 4H), 7.01 4 6.89 (m, 4H), 6.87 (d, J: 5.3 calcd Hz, 1H), 5.73 (dq, J: 9.7, 6.1 Hz, 1H), 92 ——— ——— calcd for 4.59 2 4.49 (m. 11-1). 405 (d. J: 9.8 Hz.
CZSHEFZNZOS. 1H). 3.94 (s. 3H). 1.25 (d. J: 6.2 Hz. 471.1731; 3H), 1.07 (d,J= 7.2 Hz, 3H) found, 471.1735 ”F NMR (376 MHz. ~,)5 6, —115.80 1H NMR (400 MHz, CDClg) 5 12.03 (d, J : 0.7 Hz. 1H). 8.40 (d. .1: 8.1Hz. 1H). 7.97 (d. J: 5.2 Hz. 1H). 7.41 4 7.09 (m. 10H), 6.85 (d,J= 5.2 Hz, 1H), 5.97 (q, J HRMS—ESI = 6.3 Hz, 1H), 4.61 (dq, J: 8.2, 7.2 Hz, (/77 z) 1H). 3.94 (s. 3H). 3.39 (dq. J: 9.1. 6.9 [2M+Nar Hz, 1H), 3.18 (dq,J: 9.2, 6.9 Hz, 1H), calcd for 1.30 (d, J: 7.2 Hz, 3H), 1.17 (t, J: 6.9 C54HMN4NaOIZ. Hz. 3H). 1.13 (d. J: 6.3 Hz. 3H) 979.4106; found, 13C NMR (101 MHz, CDC13) 5 171.45, 979.4119 168.56,155.34,148.71, 141.84, 140.56, . . 128.25. 127.87. 127.81. 127.69,127.33,127.21, 109.41, 84.05, 74.30, 59.93, 56.08, 48.05, 18.02, 15.67, 14.95 1H NMR (300 MHz. CDCL.) 5 1204 (d. J = 0.6 Hz, 1H), 8.41 (d, J: 8.0 Hz, 1H), 7.97 (d,J= 5.2 Hz, 1H),7.41— 7.18 (m, HRMS'ESI, 10H). 6.85 (d. J: 5.4 Hz. 1H). 5.97 (q. J [MfgCZHr : 6.3 Hz, 1H), 4.75 4 4.49 (m, 1H), 3.94 (3, 3H), 3.15 (s, 3H), 1.29 (d, J: 7.2 Hz, calcd f0} 95 3H). 1.13 (d. .1: 6.3 Hz. 3H) 4311761 13C NMR (101 MHz, CDC13) 5 171.42, found, 168.58,155.35,148.72,141.11.140.39, 433.1763 139.89. 130.37. 128.51. 128.11. 127.86. 127.69. 127.52, 127.31, 109.42, 84.47, 74.02, 56.08, 52.55, 48.05, 17.97, 14.97 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NIVIR N0. (‘0 (cm'l) (1H, 13C. 191:) 1H NMR (400 MHz, CD03) 5 12.03 (d, J = 0.6 Hz, 1H), 8.31 (d, J: 7.9 Hz, 1H), 7.97 (d, .1: 5.2 Hz, 1H), 7.35 (td, .1: 8.5, 6.2 Hz, 1H), 7,23 (td, J : 8.4, 6.2 Hz, 1H), 6.91 4 6.74 (m, 4H), 6.69 (ddd, J: .4, 8.8, 2.6 Hz, 1H), 5.88 4 5.74 (m, 1H), 4.69 (d, .1: 9.9 Hz, 1H), 4.64 4 4.48 (m, 1H), 3.95 (s, 3H), 1.30 (d,J= 6.1 Hz, 3H), 1.17 (d,J= 7.2 Hz, 3H) ”P NMR (376 MHz, CDC13)8 -110.97 (d,J= 7.7 Hz), -111.39 (d, J: 76 Hz), 41 1 1.98 (dd, .1: 7.7, 2.6 Hz), 4 112.83 (dd, .1: 7.6, 2.6 Hz) 1H NMR (400 MHz, CDC13) 5 12.06 (s, 1H), 8.31 (d,J= 7.9 Hz, 1H), 7.98 (61.1: .2 Hz, 1H), 7.49 4 7.40 (m, 4H), 7.37 4 7,24 (m, 5H), 7,23 4 7.18 (m, 1H), 6.86 (d, J: 5.2 Hz, 1H), 6.00 (dq, J: 25.4, 97 6.4 Hz, 1H), 4.63 4 4,51 (m, 1H), 3.94 (s, 3H), 1.32 (dd, .1: 6,5, 1.0 Hz, 3H), 0.96 (d, J: 7.2 Hz, 3H) ”P NMR (376 MHz, CD(‘,1~,) 5 -169.17 1H NMR (400 MHz, CDClg) 5 12.11 (s, 1H), 8.35 (d, .1: 8.0 Hz, 1H), 7.97 (d, .1: .2 Hz, 1H), 7.22 4 7.12 (m, 4H), 6.90 4 HRMS—ESI 6.73 (m, 5H), 5.73 (dq, J: 9.8, 6.1 Hz, (m z) 1H), 4.64 4 4,44 (m, 1H), 3.96 (d, J: 9.9 (| M+H F) Hz, 1H), 3.93 (s, 3H), 3.75 (s, 3H), 3.73 calcd (5,311), 1.24 (d, .1 : 6.2 Hz, 3H), 1.05 (d, 98 calcd for J: 7.2 Hz, 3H) N2074 495 .2 13 l ; ”C NMR (101 MHz, CDCL.) 5 171.65, found, 168.54,158.36,158.20,155.34,148.70, 24 140.40,133.83,133.69, 130.45, 128.97, 128.92, 11411, 113.81, 109.39, 7377, 5611, 56.04, 55.20, 55.19, 47.90, 1920, 17.75 [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13)8 12.05 (s, SI 1H), 8.34 (d, J: 8.0 Hz, 1H), 7.98 (d, J: (m z) 5.3 Hz, 1H), 7.32 4 7.19 (m, 2H). 7.1 1 4 ([M4Hr) 703 (111,211), 7.02 4 6.83 (m, 5H), 5,75 calcd (dq,J= 9.8, 6.1 Hz, 1H), 4.65 4 4.46 (m, 99 calcd for 1H), 4.06 (d, .1: 9.9 Hz, 1H), 3.94 (s, CZSHEFZNZOS, 3H), 1.27 (d, .1: 6.1 Hz, 3H), 1,07 (d, .1: 471.1731; 7.2Hz, 3H) found, 4711724 ”F NMR (376 MHz. CD(‘,1~,) 5 7, -112.48 1H NMR (400 MHz, CDClg) 5 12.04 (s, 1H), 8.32 (d, .1: 7.7 Hz, 1H), 7‘98 (01, .1: .3 Hz, 1H). 7.31 4 7.10 (m, 8H), 6.86 (d, HRxSZfSI J: 5.2 Hz, 1H), 5.73 (dq, J: 9.9, 6.2 Hz, 1H), 4.60 4 4.48011, 1H), 4.01 (d, J: ([NHHT) .0 Hz; 1H), 3.94 (s. 3H), 1.27 calcd (51, .1: 6.2 Hz, 3H), 1.08 (d, J4 7.1 Hz, 3H) 100 calcd for C$3€11E)0 13C NMR (101 MHz. CDC1,)5 17155, ‘ found ‘ 168.60, 155,36, 14872. 142.54, 142.33, 140.47, 134.73, 134.42, 130.33, 130.23, 503 1137' 129.94,128.42,128.33, 127.52, 127.21, 126.18, 125.98, 109.47, 72.83, 57.03, 56.08, 47.85, 1911,1766 HRMS—ESI 1H NMR (400 MHz, CDClg) 5 12.23 4 (m z) 11.94 (m. 1H), 8.64 4 8.39 (m. 1H), 8.11 (119141115 4 7.92 (m. 1H), 7.78 4 7.60 (m, 3H), 7.59 calcd 4 7.48 (m, 1H), 7.46 4 7.35 (m, 2H), 7.36 101 calcd for — 7.26 (m, 1H), 7.27 4 7,20 (m, 1H), 6.91 (725113514205, 4 6.84 (m. 1H), 5.87 4 5.69 (m, 1H), 4.94 433.1763; 4 4.76011, 1H), 4.35 4 4,22 (m, 1H), 400 found, — 3.93 (m, 3H), 1.69 — 1.51 (m, 3H), 0.95 4331749 4 0.59 (m. 3H) HRMS-ESI (m z) 1H NMR (400 MHz, CDC13) 5 12.16 (s, ([M+H]+) 1H),8.514 8.38011, 11— 7.82 (m, calcd 1H), 7.34 4 7.15 (m. 4H), 7.15 4 6.94 (m, 102 ——— ——— calcd for 4H), 6.91 2 6177 (m, 1H), 5120 2 5.09 (m, C25H35N306, 1H), 4.78 4 4.64011, 1H), 4.33 4 4.17 (m, 449.1712; 1H), 3.96 4 9.92 (m, 3H), 1.55 4 1.42 (m, found, 3H), 1.104091 (m. 311) 449.1707 [Annotation] an None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. ”C. 191:) 1H NMR (400 MHz, CDC13) 5 12.06 (s, 1H), 8.33 (d,J= 7.9 Hz, 1H), 7.97 (d,J= .2 Hz. 1H). 7.50 4 7.31 (m. 4H). 7.24 4 “113717551381 7.01 (m, 4H), 6.87 (d, J: 5.2 Hz, 1H), .73 (dq, J: 9.6, 6.1 Hz, 1H), 4.55 (p,J ([M+H]+) : 7.3 Hz. 1H). 4.01 (d. .1: 9.7 Hz. 1H). calcd 3.93 (s. 3H). 1.25 (d;./: 6.1 Hz. 3H). 103 calcd for 1.09 (d, J— 7.2 Hz, 3H) CstszerzOs, 5910130; 12, (, NMR_(_101 MHz. CD(,1~,) 5 171.50.4 4 4 4 _ found 168.61.155.3914874,140.47, 139.69, 591 012‘;' “ 139.59,132.00,131.69, 130.31, 129.80, 129.73.121.12.120.84. 109.52.72.81. 56.45. 56.08. 47.86. 19.09. 17.67 1H NMR (400 MHz, CDC13) 5 12.13 (s, 1H), 8.44 (d,J= 8.0 Hz, 1H), 7.99 (d,J= .2 Hz. 1H). 6.87 (d. .1: 5.2 Hz. 1H).
HRMS-ESI 6.73 (d, J: 3.4 Hz, 1H), 6.67 (d, J: 3.4 (m z) Hz, 1H), 6.54 4 6.35 (m, 2H), 5.54 4 5.40 (1M4Hr) (m. 1H). 4.78 4 4.59 (m. 1H). 4.45 (d. .7: calcd 7.1 Hz. 1H). 3.94 (s. 3H). 2.39 (s. 6H). 104 calcd for 1.30 (d, J: 2.8 Hz, 3H), 1.28 (d, J: 3.7 C33H3-Ngossg, Hz, 3H) 475.1361; found, ”C NMR (101 MHz, CDC13) 5 171.50, 475.1368 168.60,155.35,148.74, 141.52, 140.47, 140.41. 139.03. 139.00. . 125.76. 125.08. . 124.42. 109.41. 74.68. 5607,4800, 47.84, 18.65, 17.88, 15.25 1H NMR (400 MHz, CDC13) 5 12.14 (s, 1H). 8.38 (d. .1: 8.0 Hz. 1H). 7.94 (d. .1: .2 Hz, 1H),7.214 7.10 (m, 4H), 7.09 4 6.97 (m, 4H), 6.82 (d, J: 5.2 Hz, 1H), HRSiSZfSI, 5.79 (dq. .1: 10.1. 6.2 Hz. 1H). 4.53 (p. .7 : 7.3 Hz. 1H). 3.98 (d. .1: 10.0 Hz. 1H). (1MMy) 3.88 (s, 3H), 2.25 (s, 3H), 2.23 (s, 3H), calcd _ 1.25 (d, J: 6.3 Hz, 3H), 1.01 (d, J: 7.2 105 ——— ——— calcd for Hz 3H) C27HEINZOS~ ‘ 5 42312131 ”C NMR (101 MHz, CDC13) 5 171.66, 168.57. 155.32. 148.71. 140.43. 138.63. 463.2242 . 136,37. 136.05. 130.45. 129.44. 129.11,127.91,127.85, 109.45, 73.66, 57.08. 56.02, 47.92, 20.97, 20.93, 19.24, 17.64 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. ()0 (cm'l) (H, ”C, 191:) 1H NMR (400 MHz, CDClg) 5 12.09 (s, , 1H), 8.35 (d,J= 8.0 Hz, 1H), 7.97 (01.1: HRR’IS'ESI .2 Hz, 1H), 7.54 (d, .1: 8.1 Hz, 2H), ([?ig? 7,42 (d, J: 8.1 Hz, 2H), 7.34 4 7.21 (m, 4H), 7.21 4 7.13 (m, 1H), 6.86 (d, J: 5.2 calcd Hz, 1H), 5.85 (dq, .1: 9,8, 6.1 Hz, 1H), 106 calcd for 4.614 4,46 (m, 1H), 4. 15 (d, .1 : 9.9 Hz, C) H) F~N7O- 50361794 1H), 3.93 (s, 3H), 1.27 (5,11: 6.2 Hz, 3H), 1.00 (d, J— 7.2 Hz, 3H) found 3011794 ”P NMR (376 MHz, CDC13)8 -62.53 1H NMR (400 MHz, CDC1~,) 5 12.05 (s, 1H), 8.32 (d, .1: 8.0 Hz, 1H), 7,97 (d, .1: HRMS—ESI 5.2 Hz, 1H), 7.38 4 7.10 (m, 8H), 6.87 (d, (777 z) J: 5.2 Hz, 1H), 5.73 (dq, J: 9.9, 6.2 Hz, (| M+H|+) 1H), 4.62 4 4.45 (m, 1H), 4.03 (d, .1: 9.6 calcd Hz, 1H), 3.94 (s, 3H), 1.25 (d, J: 6.1 Hz, 107 calcd for 3H), 1.09 (d, J: 7.2 Hz, 3H) C25H25C12N2054 503.1140; ”C NMR (101 MHz, CD07.) 5 171.52, found, ,155.41,148.74, 140.45, 139.26, 503.1139 139.15,133.04,132.77,1303212941, 129.36, , 128.73, , 7295, 5635, 56.08, 47.86, 19.08, 17.67 1H NMR (400 MHz, CDClg) 5 12.10 (s, 1H), 8.36 (d, .1: 7.9 Hz, 1H), 7.95 (d, .1: .2 Hz, 1H), 7.57 4 7.46 (m, 8H), 7.43 4 7.38 (m, 7H), 7.34 4 7.29 (m, 2H), 6,81 (d,J= 5.2 Hz, 1H), 5.90 (dq,J= 12.2, 6.1 Hz, 1H), 4.56 (p, .1: 7.2 Hz, 1H), 4.16 (d, J: 100 Hz, 1H), 3.89 (d, J: 1.9 ESIMS Hz, 3H), 1.34 (51,]: 6.1 Hz, 3H), 1.02 W Z 587 109 (d, .1: 7.2 Hz, 5H) (I M+H|+) 13C NMR (101 MHz, CDC13) 5 171.71, 168.59,155.33,148.72, 140.65, 140.58, 140.43, 140.11, , 139.66, 130.44, 128.77,128,73,128.67, 128.53, 127.58, 127.30,127.26,127.21, 127.00, 126.94, 109.40, 73.58, 57.25, 5604, 47.91, 19.33, 17.66 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) (Thin 3374, 2984, 1H NMR (400 MHz, CDC13)8 11.80 (s, 1735, 1H), 8.30 (d,J= 8.0 Hz, 1H), 8.07 (dd,J 1649, : 4.3, 1.5 Hz, 1H), 7.40 4 7.15 (m, 6H), 1602, 7.05 4 6,85 (111,4H), 5.73 (dq, .1: 9.8, 6.2 1577, Hz, 1H), 4.65 — 4.45 (m, 1H), 4.05 (d, J: 1530, HRMS—ESI 9.8 Hz, 1H), 1.25 (d, J: 6.1 Hz, 3H), 1507, (m z) 1.07 (d, .1: 7.2 Hz, 3H) 1449, (1M4Hr) 1380, calcd ”C NMR (101 MHz, CDC13) 5 171.60, 1 10 1329, calcd for 168.26, 16 1 .76 (d, .1: 246.1 Hz), 161.64 1296, (734H13F3N304, (d, .1: 2457 Hz), 157.79, 139.65, 136.82 1222, 441.1620; (d,J= 3.3 Hz), 136.71 (d,J= 3.5 Hz), 1188, found, 13104, 129.50 (d,J= 7.9 Hz), 128.80, 1159, 4411620 , 115,74(d,.1: 21.3 Hz), 115.41 1130, (d,J: 21.3 Hz), 7334, 56.14, 47.84, 1105, 19.12, 17.69 1049, 1015, 906, ”P NMR (376 MHz, CD(‘,1¢.)5 826, 809, -115.44, -11576 792, 778, 731, 704, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) (Thin 3370, ‘HNMR (400 MHz, CD(‘,1~,)5 1206 (d, J 2984, : 06 Hz, 1H), 8.33 (d, J: 8.0 Hz, 1H), 2936, 7.95 (d, J: 5.2 Hz, 1H), 7.35 — 7.14 (m, 2256, 4H), 7.04 4 6,87 (m, 4H), 6.84 (d, .1: 5.2 1735, Hz, 1H), 5.73 (dq,.1: 9.7, 6.1 Hz, 1H), 1647, 8 (m, 1H), 4.16 (q,J= 7.0 Hz, 1604, “Eff“, 2H), 4.05 (d, J: 9.7 Hz, 1H), 1.51 (t, J: 1574, 7.0 Hz, 3H), 1.24 (d, .1: 6.1 Hz, 3H), 1:32 1,06 (d, J 72 Hz, 3H) ([M+H]+) 1483, 1 11 0,333?“ 13C NMR (101 MHz, 5 171,58, 1469, 168.66, 161.75(d,.1: 2461 Hz), 161.64 C7 H7—F7N70- 1452, ‘28; 1883- (d,J= 2457 Hz), 154.75, 148.82, 1381, 16mm = 140.38,136.82(d,J= 3.3 Hz), 13673 (d, 1323, .1: 3.3 Hz), 130.41, 12951 (d, .1: 7.6 48, 1m) 1281, 5' Hz), 115.72(d,J:21.411z), 115.39(d,J 1262, = 21.2 Hz), 110.13, 467, 5612, 1222, 4784,1911, 1769,1437 1 158, 1109, ”F NMR (376 MHz, CDC13) 8 1048, -115.47, -115.80 1015, 990, 904, 824, 800, 730 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) (Thin 3370, 2984, 1H NMR (400 MHz, CDC13)8 12.05 (s, 1729, 1H), 7.43 — 7.33 (m, 2H), 7.30 — 7.17 (m, 1641, 4H), 7.05 4 6,90 (m, 5H), 6.88 4 6,77 (m, 1601, 2H), 5.75 (dq, .1: 9,9, 6.1 Hz, 1H), 4.57 1531, (p,J=7.l Hz, 1H),4.06(d,J=9.9 Hz, 1507, HRMS—ESI 1H), 1.25 (d, J: 6.1 Hz, 3H), 1.00 (d, J: 1491, (m z) 7.1 Hz, 3H) 1450, (1M4Hr) 1361, calcd ”C NMR (101 MHz, CDC13) 5 172.22, 112 1305, calcd for , 16 1 .79 (d, .1: 246.2 Hz), 161.70 1281, CZSHNFJNOd, (d, .1: 2459 Hz), 161.59, 136.83 (d, .1: 1254, 440.1668; 3.4 Hz), 136.61 (d,J= 3.4 Hz), 134.49, 1222, found, 12949 (d, J: 8.1 Hz), 12946 (d, J: 7.9 1177, 4401676 Hz), 125.62, 118.70, 118.58, 11579 (d, .1 1158, :21.4Hz), 115.50 (d,J:21,3 Hz), 1135, 113.72, 73.62, 56.17, 48.29, 19.15, 17.79 1087, 1048, ”P NMR (376 MHz, C190,) 5 08, -115.30,-115.60 824, 778, 752, 731, 1H NMR (400 MHz, CDClg) 5 11.98 (d, J : 0.6 Hz, 1H), 8.30 (t, .1: 5.7 Hz, 1H), 7.99 (d, .1 : 5.2 Hz, 1H), 7.24 4 7.15 (m, 4H), 7.03 — 6,85 (m, 5H), 5.71 (dq, J: 9.2, 6.2 Hz, 1H), 4.11 (dd,J= 18.1, 6.0 Hz, 1H), 4.04 (d, .1: 9.2 Hz, 1H), 3.95 (s, ESIMS 3H), 3.90 (dd, J: 18.1, 5.6 Hz, 1H), 1,25 m/Z 457.6 (d, J: 6.3 Hz, 3H) (HWHT) ”C NMR (101 MHz, CDCI3) 5 169.18, 168.43,161.74(d,J= 246.1 Hz), 161.63 (d,J=245.5 Hz), 155.42, 148.71, 140.55, 136.68, 130.30, 129.68, , 115.67 (d,J: 29.2 Hz), 115.46 (d,J: 29.1 Hz), 109.55, 73.65, 56.11, 55.77, 40.91, 19.12 [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NIVIR N0. (‘0 (cm'l) (1H, 13C. 191:) 1H NMR (400 MHz, CDC13) 5 12.08 (s, 1H), 8.32 (d,J= 8.5 Hz, 1H), 7.98 (61.1: .2 Hz, 1H), 7.46 4 7.04 (m, 4H), 7.1 1 4 6.65 (m, 5H), 5.71 (dq, J : 9.8, 6.2 Hz, 1H), 4.51 (ddd,J= 8.5, 7.0, 5.4 Hz, 1H), 4.05 (d, .1: 9.6 Hz, 1H), 3.95 (s, 3H), 1.704 1,57 (m, 1H), 1.49 4 1.36 (m, 1H), ESIMS 1.24 (d, J: 6.2 Hz, 3H), 0.67 (t, J: 7.5 m 2 485.6 Hz, 3H) (| M+H |+) ”C NMR (101 MHz, CDC13) 5 170.87, 168.79,161.74(d,J= 245.9 Hz), 161.66 (d, .]:245.8 Hz), , 148.73, 140.42, 136,80, 13036, 129.55 (d, .1: 2.7 Hz), 129.47 (d, J: 2.7 Hz), 115.67 (d, J: 32.4 Hz), 115.45 (d, J: 32.4 Hz), 109.44, 73.48, 56.09, 56.03, 53.16, 25.16, 19.18, 9.27 1H NMR (400 MHz, CDClg) 5 12.08 (d, J : 0.6 Hz, 1H), 8.32 (d, .1: 9.4 Hz, 1H), 7.98 (d, .1: 5.2 Hz, 1H), 7.31 4 7.07 (m, 4H), 6.97 (t, J: 8.6 Hz, 2H), 6.93 — 6.86 (m, 3H), 5.72 (dq, J: 9.7, 6.2 Hz, 1H), 4.48 (dd, .1 : 9.4, 4.7 Hz, 1H), 4.05 (d, .1 : 9.7 Hz, 1H), 3.95 (s, 3H), 1.93 4 1,82 (m, 1H), 1.23 (d, J: 6.1 Hz, 3H), 0.82 ESIMS (d, .1: 6.9 Hz, 3H), 0.65 (d, J: 6.8 Hz, m 2 499.6 (UVHHY) ”C NMR (101 MHz, CDC13) 5 , 168.95, 16173 (d, .1: 2464 Hz), 161.65 (d,J:245.6 Hz),155.43, 148.71, 140.42, 136.85, 130.40, 129.54 (d,J= 4.7 Hz), 12947 (d, .1: 4.7 Hz), 11571 (d, .1: 21.3 Hz), 11540 (d, .1: 21.3 Hz), 109.43, 73.51, 57.09, 56.09, 55.98, 30.96, 19.22,19.10,17.10 [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 8 12.07 (d, J = 0.6 Hz, 1H), 8.15 (d, J: 8.9 Hz, 1H), 7.97 (d. .1: 5.2 Hz. 1H). 7.31 4 7.04 (m. 4H), 7.08 4 6.74011, 6H), 5.70 (dq, J: .0, 6.1 Hz, 1H), 4.54 (ddd, J: 9.7, 8.8, .0 Hz. 1H). 4.04 (d. .1: 9.8 Hz. 1H). 3.94 (s. 3H). 1.46 4 1.36 (m. 1H). 1.33 4 1.18 (111,4H), 1.08 (ddd: J: 13.9, 9.0, 5.0 ESIMS Hz, 1H), 0.82 (EU: 6.5 Hz, 3H), 0.77 m Z 5137 116 (d. .14 6.6 Hz. 3H) (I WHF) ”C NMR (101 MHz, CDC13) 8 171.62, 168.81. 161.75 (d. .1:246.2 Hz). 161.66 (d..1:245.6 Hz). 155.43. 148.74. 140.39,137.02,136.76, 130.34, 12951 (d, J: 3.4 Hz), 129.44 (d, J: 3.5 Hz), 115.73 (d..]:21.4 Hz). 115.41 (61.1: 21.3 Hz), , 73.37, 56.21, 56.09, 50.52, 41.00, 24.57, 22.76, 21.49, 19.14 1H NMR (300 MHz.CDC1~.)5 1215 (d. J (Thin : 0.6 Hz. 1H). 8.38 (d. .1: 8.0 Hz. 1H). ?lm) 7.97 (d, J: 5.2 Hz, 1H), 7.45 (dd, J: 3368, (“$313 7.6, 1.7 Hz, 1H), 7.30 4 7.20 (m, 1H), 2937. 7.12 (dddd..1: 13.5. 8.1. 7.5. 1.7 Hz. calcd for 117 1732, 2H), 6.92 4 6.80 (m, 4H), 6.76 (dd,J: C H N 0 1648, $953136?) 8.2, 1.1 Hz, 1H), 5.97 (dq,J= 9.0, 5.7, 1527. {6111161 ‘ 5.2 Hz. 1H). 5.01 (61.1: 10.1 Hz. 1H). 1241. 4.70 4 4,39 (m. 1H). 3.93 (s. 3H). 3.85 (s. 49, 2164 1144 " 3H), 3.75 (s, 3H), 1.25 (d, J: 6.2 Hz, 3H), 1.01 (d, J: 7.2 Hz, 3H) :W1(iii?2““25‘301’S1hi'11‘ii?"z. .35 : £13122 HR?SZ'ESI . . . . . . 7.98 (d, J: 5.2 Hz, 1H), 7.21 (t, J: 8.0 2937’ Hz. 1H). 7.15 (LJ: 7.9 Hz. 1H).6_934 (1M+H|+) 1773 4‘ 6.81 (m. 5H). 6.74 (ddd../: 8.2. 2.6. 0.9 calcd 118 1648’ Hz, 1H), 6.68 (ddd,J= 8.2, 2.6, 0.9 Hz, C77H~ N707 ”27’ 419;;12‘6‘ = 1H), 5.80 (dq,J= 10.3, 6.1 Hz, 1H), 4.60 1‘26 1‘ 156111161 ‘ 4 4.43 (m. 1H). 3.99 (d. .1: 10.3 Hz. 1H). 3.94 (s, 3H), 3.77 (s, 3H), 3.75 (s, 3H), 1 148‘ 49, 2106 1041’ " 1.26 (d,J= 6.0 Hz, 3H), 1.00 (d,J= 7.2 Hz. 3H) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) (Thin ?lm) 1HNMR (300 MHz, CDClg) 5 11.92 (s, HRMS'ESI, 3367, 1H), 8.36 (d, .1: 8.1 Hz, 1H), 7.95 (d, .1: 2985, “Sign 52 Hz, 1H), 777 (t, J: 8.5 Hz, 1H), 1738, 7.37 (t, J: 8.5 Hz, 1H), 7.15 (ddd, J: Galed for 119 1647, 8,5, 2.1, 07 Hz, 1H), 70846.89 (m, (,rHerRMO 1575, 5‘55 0896; "* 3H), 6.86 (5,.1: 5.3 Hz, 1H), 6.10 (q, .1: 1481, “ 151111 * 62 Hz, 1H), 4.66 (p, J: 7.3 Hz, 1H), 1263, 3.95 (s, 3H), 3.22 (s, 1H), 1.36 (d,J= 7.2 555 0909 1153, “7' Hz, 3H), 1.24 (d, .1: 6.3 Hz, 3H) 1058, 914 ($111; 1H NMR (300 MHz, CDClg) 5 12.06 (d, J : 0.6 Hz, 1H), 8.34 (d. .1: 8.0 Hz. 1H), 3369 (m Z) ‘2‘934‘ 7,98 (d, J: 52 Hz, 1H), 7.16 4 7.01 (m, ([M+H]+) 173; 2H), 7.01 4 6.79 (m, 5H), 5.70 (dq, J: 031Cd for 120 1648’ 99,61 Hz, 1H), 4.70 4 4.43 (m, 1H), (,7 H71 RN70 1576* [4992039 3.97 (d, .1: 9.3 Hz, 1H), 3.94 (s, 3H), 1ng fo11nd * 2.20 (d,J= 19 Hz, 3H), 2.17 (d, J: 1.9 i- ’ : , Hz,3H), 1.25 (d,J= 6.1 Hz, 3H), 1.09 1451, 4992050 (d 1:?2HZ 3H) 1261 *' ‘ “ mm 1H NMR (300 MHz CDClg) 5 12 14 4 £1112? HR?’IS')ESI 1 1.95 (m, 1H), 8.33 (d, .1: 8.0 Hz, 1H), 2980‘ (MEN) 7.98 (d, .1 : 5.2 Hz, 1H), 7.21 (d. .1: 1.5 1735’ Hz, 2H), 7.19 4 6.99 (m, 4H), 6.86 (d, J: calcd for 121 1648= 5.2 Hz, 1H), 5.69 (dq, J: 9.8, 6.1 Hz, C7 H71C17N70- ”27* 533,1) 1448 1H), 4.55 (p,./: 7.3 Hz, 1H), 3.94 (51,7: 1450* ”fo'und * 99 Hz, 1H), 3,94 (s, 3H), 2.31 (s, 3H), 1262= 531 14328 2.27 (s, 3H), 1.25 (d, J: 6.0 Hz, 3H), ' ' ' 1,10(d,.]:7,2Hz,3H) 1H NMR (300 MHZ, CDC13)8 12.00 (d, J (Thin = 0.6 Hz, 1H), 8.41 (d, J: 8.1 Hz, 1H), 7,97 (d, .1: 5.2 Hz, 1H), 7.87 4 7,75 (m, 3,67 HRMSESI 3986* 1H), 7.48 (11.1: 8.0. 1.5 Hz, 1H). 7.28 4 (W Z) 1737’ 7.12 (m, 3H), 7.10 4 6.98 (m, 1H), 6.99 4 ([M+H]+) 164; 6.86 (m, 2H), 6.90 4 6.82 (m, 1H), 6.26 calcd for 122 1611* (qd, .1: 6.3, 1.5 Hz, 1H), 4.73 4 4.57 (m, _F7N7O 1482* [187:107? "* 1H), 3.94 (s, 3H), 3.19 (dd,J: 2.8, 1,9 = ' ” Hz, 1H), 1.28 (d,J= 6.3 Hz,3H), 1.27 1432,_, found, (d I: 7 2 Hz RH) 1215, 4871686 *' ' *‘ 1110:: 19F NMR (471 MHz, CDC13) 5 -111.85 4 4112.11 (1H),-112.15 4 4112.47 (111) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. ”C. 191:) ($11“ 1H NMR (400 MHz. CDC13) 8 12.06 (d, J 32;“? HRMS ESI (/77 2') : 0.6 Hz. 1H). 8.33 (d. .1: 8.0 Hz. 1H). ‘298‘1‘ 7.98 (d. .1: 5.2 Hz. 1H). 7.45 4 7.40 (m. (1MMy) 2107’ 2H), 7.40 — 7.35 (m. 2H). 7.28 — 7.18 (m, calcd for 123 = 4 4H), 6.86 (d, .1: 5.2 Hz, 1H), 5.78 (dq, J 1736. C29HerO5. — . . , ,49.8. 6.1 Hz. 1H).4.61 44.45 (m. 1H). 1648 4. “28‘ f01111d * 4.07 (d, J: 9.8 Hz, 1H). 3.94 (s. 3H). {263’ 3.05 (s. 1H). 3.03 (s. 1H), 1.25 (d.J= 6.2 483 19 1’9 ’ ' - Hz. 3H). 10401.1: 72 Hz. 3H) (Thin £122 1H NMR (400 MHz. CDC13) 5 12.12 (s, 2963* HRMS-ESI 1H). 8.37 (d. .1: 8.0 Hz. 1H). 7.98 (d. .1: 1735* (/77 z) 5.2Hz,1H),7.244 7.18 (111,411). 7.144 164E; ([M+H]+) 7.08 (m. 2H). 7.08 — 7.02 (m, 2H). 6.85 124 ”27’ calcd for (d..1:5.2 Hz. 1H). 5.80(dq..I: 10.1. 1480‘ CnggNzOs. 6.2 Hz. 1H). 4.63 4 4.40 (m. 1H). 3.99 (d. 1450’ 491.2540; J: 10.2 Hz. 1H), 3.93 (s, 3H), 2.65 — 1280’ found, 250 (m. 4H). 1.25 (d. J: 6.1 Hz. 3H). 126.; 491.2551 1.1851,]:76 Hz.3H)_ l.l4£t..]:7.6 Hz. 3H). 0.94 (4.14 7.2 Hz, 3H) 1142, ‘H NMR (400 MHz. CD(‘,1~,)5 1208 (d. .1 : 0.6 Hz. 1H). 8.33 (d. J: 8.0 Hz. 1H). 7.98 (d. J: 5.2 Hz. 1H), 7.32 — 7.20 (m, 5H). 7.19 4 7.10 (m. 1H). 6.97 (1. .1: 8.7 Hz. 2H). 6.86 (d. .1: 5.2 Hz. 1H). 5.78 HRgisz'fSl (dq, J: 10.0. 6.2 Hz. 1H). 4.58 — 4.45 ([M+H]+) (m. 1H). 4.05 (d, J: 10.0 Hz, 1H). 3.94 (s. 3H). 1.26 (d. .1: 6.2 Hz. 3H). 0.98 (d. calcd for 12$ ___ ___ J: 7 2 Hz 3H) FNZOS: ‘ 5' 431931130 13C NMR (126 MHz. CDCL.) 8 171.63. 168.54. 161.72 (d..1:245.7 Hz). 155.35. . -4 ; 433.1851 148.71,141.10,140.41.136.91(d.J= 3.5 Hz).130.42,129.58(d. J: 7.8 Hz), 128.59. 127.95. 126.84. 115.64 (d. .1: 21.3 Hz). , 73.39, 57.04, 56.07, 4783.19.15, 17.59 [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NIVIR N0. (‘0 (cm'l) (1H, 13C. 191:) 1H NMR (400 MHz, CD03) 8 11.77 (d, J = 0.6 Hz, 1H), 8.25 (d, J: 8.0 Hz, 1H), 7.96 (d. .1: 5.2 Hz. 1H). 7.53 (dd. .7: .0, 2.2 Hz, 2H), 7.35 (dd, J: 8.5, 1.8 Hz, 2H), 7.18 (ddd,J= 10.9, 8.5, 2.3 Hz, 2H). 6.88 (d. .1: 5.2 Hz. 1H). 5.80 (q. .7: ESIMS 6.3 Hz. 1H). 4.68 4 4.47 (m. 1H). 3.95 (s. m 2 589.5 3H), 1.27 (d, J: 7.3 Hz, 3H), 1.20 (d, J: ([M+H]+) 6.4 Hz, 3H) ”C NMR (126 MHz, CDC13)8 17098, 168.86,155.52,148.74,1441814199, 140.57. 132.92. 132.87. 132.02. 131.86. 130.48. 130,37. 12991. 128.15. 127.74. 125.09, 124.82, 109.64, 78.58, 74.60, 56.11, 48.05, 1756,1413 1H NMR (400 MHz. CD(‘,1~,)8 1 1.78 (d. .1 : 0.6 Hz, 1H), 8.25 (d, J: 8.0 Hz, 1H), 7.96 (d, J: 5.3 Hz, 1H), 7.33 — 7.27 (m, 2H). 7.22 (dd. .1: 10.4. 2.2 Hz. 1H). 7.08 (dddd. .1: 19.0. 8.5. 2.1. 0.8 Hz. 2H). 6.88 (d,J= 5.2 Hz, 1H), 5.82 (q, J: 6.3 Hz, 1H), 4.65 — 4.51 (m, 1H), 3.95 (s, 3H). 3.00 (s. 1H). 1.26 (d. .1: 7.2 Hz.
ESIMS 3H), 1.20 (d, J: 6.3 Hz, 3H) m/z 333 .6 ([M+H]+) 13C NMR (126 MHz. CDC1~,) 8 . 168.87. 15804 (d. .1: 249.8 Hz). 157.99 (d,J=249.5 Hz), 155.54, 148.76, 145.02 (d,J= 5.5 Hz), 142.77 (d,J= 6.0 Hz), . 130.65. 130.55. 129.94. 122.05 (d,J: 3.7 Hz), 121.65 (d,J: 3.6 Hz), 120.45 (d, J: 17.8 Hz), 120.25 (d, J: 17.7 Hz). 114.56 (d. .1: 22.7 Hz). 114.26 (d. .1: 23.0 Hz). 109.62. 78.63. 74.64. 56.12, 48.02, 17.52, 14.30 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) 1H NMR (400 MHz, CDC13) 5 12.06 (s, 1H), 8.32 (d,J= 8.0 Hz, 1H), 7.98 (d,J= .2 Hz, 1H), 7.25 (d, .1: 9.7 Hz, 1H), 719 (d, J: 8.2 Hz, 1H), 7‘09 (dd, J: , 4.0, 2.3 Hz, 2H), 7.02 (td,J= 8.5, 2.3 Hz, IHU("IS')ESI 2H), 6.87 (d, .1: 5.2 Hz, 1H), 5.71 (dq, J (MEN) : 10.0, 6.1 Hz, 1H), 4.54 (p, .1: 7.3 Hz, 1H), 3.99 — 392 (m, 4H), 2.33 (s, 3H), calcd for 129 2.29 (s, 3H), 1.24 (d, J: 6.1 Hz, 3H), C H27 29 C1 N 02 2 5. 1.07 (d, .14 7.2 Hz, 3H)2 '3 531.1448; found, 13CNMR(126MHz,CDC13)o171.61,2 531.1454 168.57, 155.39, 148.74, 140.44, , 139.35, , 136.15, 133.12, 132.77, 130.63,130.59,130.34, 129.45, 129.12, 126159, 126.41, 109.44, 73105, 56.45, 56.08, 47.85, 20.17, 2008, 19.15, 17.69 [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. ”C. 191:) (Thin 3376. 2986, 2360, 1H NMR (400 MHz. CDC13) 8 12.63 (s, 2107. 1H). 8.32 (d. .1: 7.9 Hz. 1H). 7.88 (d. J: 1736. 4.9 Hz. 1H). 7.62 (d. .1: 4.9 Hz. 1H). 1652, 7.29 — 7.15 (m, 4H). 7.05 — 6.85 (111,4H), 1604. 5.74 (dq. J: 9.9, 6.2 Hz. 1H). 4.61 — 1558. 4.48 (m. 1H). 4.05 (d. .1: 9.9 Hz. 1H). 1530, 1.25 (d,J: 6.1 Hz, 3H), 1.06 (d, J: 7.2 HRMS—ESI 15083 HZ, 3H) ,. (m z) 1452.
([M+HT) 1‘ 1427. "C NMR (101 MHz. CDCL.) 8 171.39. calcd for 130 1381, 167.69,161.76(d,J=246.1Hz).161.65 C H BrFN 0 1329, 245310769? 4’ (d,J=246.0Hz),155.39,139.43,136.82 1287. 5 161m * (d. .1: 3.4 Hz). 136.63 (d. .1: 3.1 Hz). 1262, 5210713 132.21,131.44,129.47(d,J: 8.0 Hz), 1247, ' 129.44 (c1, J: 7.9 Hz), . 115.76 (d, 1223. .1: 21.3 Hz). 115.42 (d. .1: 21.3 Hz). 1187. 73.47. 56.15. 48.05. 19.1 1. 17.61 1159, 1137, 19F NMR (471 MHz. CDC13) 5 -115.26 — 1116. —115.47(m).—115.64(ddd../: 13.7.8.9. 1049, 5.2 Hz) 1015, 911, 826. 792. 779. 729. 680, 668 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. 13C. 191:) (Thin 33 3. 2940. 1739, 1651. 1 H NMR (300 MHz. CD(,1~.) 0 1201. . - (d. .1 -’ 881211281311115:1888»..=3.z...—.m, ?g 'FSI 5H). 6.88 (d. .1: 5.2 Hz. 1H). 5.66 (dq. J 1454‘ : 9.4. 6.2 Hz. 1H). 4.64 4 4.49 (m_ 1H). (1110111) 4 ”'36: calcd for 4.01 (d, J: 9.4 Hz, 1H). 3.95 (s. 3H). 1382‘ C25H23F4N205~ 1:12 — 1.21 (111.4H). 1.16 (d. J— 7.2 Hz.3 ) 1324. 5071538; 3:; 43331433 19F NMR (471 MHz. CDC13)5 -136.05 — 1210’ ' ' ' -136.27 (111). —136.61 (ddd. J: 20.1. 11.4. 1149‘ 8.1 H21. — 39.144 —139.32 (In). 1120; 439.43 — -l39.68 (m) 1054. 954. 924. 872. 850. 824, 801. 754.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd MP IR NLASS NMR N0. (‘0 (cm'l) (1H. 13C. 191:) (11mm 3372. 2983, 1737, 1649. 1601. 1H NMR (300 MHZ,CDC13)512.02(d,J 1576, = 0.6 Hz, 1H), 8.31 (d, J: 7.9 Hz, 1H), 1529, PDRBIS-ESI 7.97 (d. .1: 52 Hz. 1H). 7.27 (td, .1: 7.3. 1498. (/77 22) 2.1 Hz. 2H). 7.194 6.98 (m. 4H). 6.88 (d. 1481, (1M+HJ+) J: 5.2 Hz, 1H), 5.66 (dq, J: 9.5, 6.1 Hz, 1453, calcd for 1H), 4.66 4 4.48 (m, 1H), 4.01 (d, J: 9.6 1439. C25H23C12F2N205.
Hz. 1H). 3.95 (s. 3H). 1.26 (d. .1: 6.2 Hz. 1381. 7; 3H),1,17(d,J: 7.2 Hz, 3H) 1323, fbund, 1245, 5590954 ”F NMR (471 MHz. CDCI.) 5 -116.83 4 1184. —1 16.94 (m). —1 17.22 4 —1 17.34 (m) 1145, 1096, 1060.953. 909.864. 849,824, 800,730, [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) (Thin 3372, 2935, 2257, 1735, 1649, 1576, 1H NMR (300 MHz, CDC13) 8 12.08 (d, J 1528, = 0.5 Hz, 1H), 8.34 (d, J: 8.0 Hz, 1H), 1501, 1112371752331, 7.97 (d, .1: 5.2 Hz, 1H), 7.12 4 6.98 (m, 1481, 5H), 6.97 4 6.79 (m, 3H), 5.70 (dq, J: ([M+H]+) 1452, 10.1, 6.1 Hz, 1H), 4.65 4 4.46 (m, 1H), calcd for 133 1439, 3,94 (s, 3H), 2.21 (dd, .1: 9.8, 1.9 Hz, C H (F N 0- 1380, 31952635, " 6H), 1.24 (d, .1: 6.1 Hz, 3H), 1.06 (d, .1: 1324, ' ‘ 7.2 Hz, 3H) found, 1281’ 499 2046 1262, ' ”P NMR (471 MHz, CD(‘,1~,)5 -119.78 4 1241, 4120.04 (m), 4120,30 4 4120.53 (In) 1206, 1 149, 1 1 18, 1051, 952, 908, 849, 821, 800, 1H NMR (300 MHz, CDC13) 8 12.08 (d, J : 0.6 Hz, 1H), 8.20 (d, .1: 8.0 Hz, 1H), 8.00 (d, .1: 5.2 Hz, 1H), 7.26 4 7.13 (m, 4H), 7.02 4 6.83 (m, 5H), 5.69 (dq, J: HRMS—ESI 90,62 Hz, 1H), 4.53 (dq, J: 8.0, 7,2 (m z) Hz, 1H), 4.05 (d, .1: 9.1 Hz, 1H), 3.96 (s, (1M4Hr) 3H), 1.34 (d, J: 7.2 Hz, 3H), 1.22 (d, J: calcd for 6.2 Hz, 3H) 135 ___ ___ F2N2054 471.1726; ”C NMR (126 MHz_CDC1~,)5171.27, found, 168.54,162.68,162.58, 160.73, 160.63, 471.1742 155.43,148.77,140.44,136.81,136.78, 136,46, 136,43, 130.33, 129.72, 129.66, 129.63,129.57,115.74,115,57,115,43, 115.26,109.49, 73,33, 5611, 55.65, 47.80, 18.95, 17.74 [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 19F) 1H NMR (300 MHz, CDC13) 8 12.00 (s, 1H), 8.30 (d,J= 7.8 Hz, 1H), 7.98 (CLJ: .1 Hz. 1H). 7.42 4 7.28 (m. 4H). 7.09 (ddd,J: 10.1, 8.3, 2.2 Hz, 2H), 6.87 (d, @1752?“ J: 5.2 Hz, 1H), 5.65 (dt,J= 12.2, 6.1 Hz. 1H). 4.57 (6.1: 7.3 Hz. 1H). 4.00 (IM+HI+) (d, ./_: 9.6 Hz. 1H). 3.95 (s, 3H). 1.27 (d, calcd for 136, J— 5.9 Hz, 3H), 1.17 (d, J— 7.2 Hz, 3H) C25H23C14N205, 371910338 ”C NMR (126 MHz. CD(‘,1~,)5 171.45. 571101367 16864, 155.42, 148.74, 140.51, , ' 140.16,133.11,132.76,131.70,131.38, 13097. 1306713027. 130.20. 13008, . 127.17. 109.53. 72.38, 56.09, 5571,47.87,19.03,17.71 1H NMR (300 MHz, CDC13) 8 11.99 (s, 1H). 8.30 (d, .1: 8.0 Hz. 1H). 7.98 (d, .1: 52 Hz, 1H), 7,42 4 7.19 (m, 2H), 7.08 4 6.94 (m, 4H), 6.90 4 6.84 (m, 1H), 5.67 (dq, J: 9.4. 6.2 Hz. 1H). 4.65 4 4.48 (m.
HRMS-ESI 1H). 4.03 (d, .1: 9.4 Hz. 1H). 3.95 (s, (m z) 3H), 1.27 (d, J: 6.1 Hz, 3H), 1.16 (d, J: ([M+H]+) 7.2 Hz, 3H) 13 ? ___ ___ cal0d for CZSHBCIZFZNZOS, 1,:C NMR (126 MHz, CDC13)0 171.41,n ,, 539.0947; 168.64,158.16(d,J= 250.2 Hz), 158.01 found, (d, .1: 2501 Hz). 155.42. 148.75. 140.91 539.0953 (d, .1 : 61 Hz). 14083 (d, .1: 6.3 Hz). 140.51,131.12,130.81,130.20,12'-'1167— 12396 (111), 12011 (d, J: 17.5 Hz), 119.82 (c1. .1: 17.7 Hz). 116.78 2 116.06 (111), 109.52, 72144, 56.09, 47.85, 18199, 17.71 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (500 MHz, CDC13)8 8.27 (d, J = 5.4 Hz, 1H), 8.13 (d, J: 8.0 Hz, 1H), 7.50 4 7.44 (111,414). 7.27 (ddd, J: 1 1.5, 8,5, 7.0 Hz, 4H), 7.20 4 714011211), SI 6.94 (d, J: 5.4 Hz, 1H), 6.01 (q, J: 6.3 (m z) Hz. 1H). 5.75 4 5.62 (m, 2H). 4.63 4 4.52 [Ml' (m, 1H). 3.90 (s, 3H). 2.94 (s, 1H)_ 2.06 calcd for (s, 3H), 1.22 (d, J: 6.3 Hz, 3H), 1.03 (d, C28H31.N308, J: 7.2 Hz, 3H) 522.2002; found, ”C NMR (126 MHz, CDC13)5 171,88, 06 170.27,163.03,160.26, 145.73, 144.99, 143.90, 142.88, 142.57. 128.31. 128.28, , 127.07, 125.56. 125.54. 109.58. 8949, 79.55, 75.21, 56.19, 48.10, 3093, 2087,1775, 1436 ‘H NMR (400 MHz. CD(‘,1~,)8 8.41 (d. .1 : 78 Hz, 1H), 8.30 (d, J: 5.4 Hz, 1H), 7.38 — 7.10 (m, 10H), 6.97 (d, J: 5.4 Hz, 1H). 5.82 (dq. .1: 10.0. 6.2 Hz, 1H). 4.52 HRMS'ES', (dt. .1: 8.2. 7.1 Hz. 1H), 4.05 (d. .1: 10.1 ($171314) Hz, 1H), 3.87 (s, 3H), 2.37 (s, 3H), 1,24 (d,J= 6.1 Hz, 3H), 0.89 (d,J= 7.1 Hz, calcd for 139 ___ ___ 3H) (TZ7H36NZO(.. 41312135 ’ ”C NMR (101 MHz, CDC13) 5 17223, 168.89. 162.28. 159.42. 146.66. 141.55, 4772019 141.44, 141,25, 137.45. 128.77. 128.50. 128.13,128.11,126.89,126.67,109.73, 73.32, 57.90, 56.27, 47.85, 20.75, 19.25, 17.92 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDClg) 8 8.35 (d, J = 7.7 Hz, 1H), 8.30 (d, J: 5.4 Hz, 1H), 7.34 4 7.09 (m, 10H), 6.95 (d, J: 5.5 Hz, 1H), 5.81 (dq, J: 10.0, 6.2 Hz, 1H), 4.62 1111103175 )ESI_ — 4.44 (m, 1H), 4.05 (d, J: 10.0 Hz, 1H), 3.85 (s, 3H), 2.93 (hept. .1: 7.0 Hz. 1H).
(I MHZ” 1.34 (d, .1: 7.0 Hz, 6H), 1.24 (d. .1: 6.2 calcd for 140 Hz, 3H), 0.88 (d, J: 7.2 Hz, 3H) C29H33N206, 3(£213 2 ”C NMR (101 MHz CD(‘,1~,) 8 174.69, 50%,2‘4 172.33, 162.28, 159.39, 146.56, 141.95, “' 3 141.45,141.27,137.61,128.76,128.50, 128.14. 128.12.126.89. 126.67, 109.58. 73.28, 57.90, 56.27. 47.83, 33.94. 19.24, 18.82, 17.96 1H NMR (400 MHz, CDClg) 8 8.25 (d, J : 5.4 Hz. 1H). 8.22 (d. .1: 7.9 Hz. 1H). 7,34 4 7.09011, 10H), 6.92 (d, J: 5.4 Hz, , 1H), 5.83 (dq,J= 10.1, 6.2 Hz, 1H), 5.72 HRE‘ISBESI (d, .1: 0.7 Hz, 2H). 4.60 4 4.49 (m. 1H), (MEN) 4.06 (d, .1: 10.1 Hz. 1H). 3.88 (s. 3H). 2.05 (s, 3H), 1,25 (d, J: 6.1 Hz, 3H), calcd for 141 0.91 (d, J: 7.2 Hz, 3H) “£23151; ”C NMR (101 MHz, CDCl;) 8 172.33, _ 170.25,162.88,160.24, 145.70, 143.91, 507.2125 142.54. 141.48.141.25. 128.76, 12849, 128.12, 128.09, 126.89. 126.65. 109.56. 8950, 73.27, 57.92, 56.17, 48.07, 20.86, 19.25, 17.73 [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) 1H NMR (400 MHz, CDC13) 5 8.28 (d, J = 7.9 Hz, 1H), 8.25 (d, J: 5.3 Hz, 1H), 7.36 4 7.08 (m. 10H), 6,92 (d, .1: 5.4 Hz. 1H), 5.83 (dq,J: 10.1, 6.2 Hz, 1H), 5.79 HRMS—ESI 4 5.69 (m, 2H), 4.62 4 4.44 (m, 1H), 4.06 (m z) (5. .1: 10.1 Hz. 1H), 3.86 (s. 3H), 2.53 (| M+H r) (hcpt, .1 : 7.0 Hz. 1H). 1.25 (d, .1 : 6.2 calcd for Hz, 3H), 1.13 (d, J: 7.0 Hz, 6H), 0.91 N307, (d. J: 7.2 HZ, 3H) 535.2444; found, ”C NMR (101 MHz, CDC13) 5 17622, 535.2431 172.34,162.85,160.23, 145.55, 144.16, . 141.48. , 128.76, 128.49, 128.12. 128,09. 12689. 126.65. 109.48. 89.90, 73.26, 57.93, 56.12, 48.07, 3385, 1926,1868, 1774 ‘H NMR (400 MHz. CD(‘,1~,) 5 8.49 (d, .1 : 8.1 Hz, 1H), 8.31 (d, .1: 5.5 Hz, 1H), 7.214 7.13 (m, 2H), 7.03 4 6.97 (111,2H), HRMS—ESI 6.95 4 6.86 (m. 3H), 5.54 (dq, .1: 7,3. 6.2 (177 z) Hz. 1H). 4.70 4 4.61 (m, 2H). 3.88 (s.
([M+H]+) 3H), 2.39 (s, 3H), 1.28 (d, .1: 6.2 Hz, calcd for 3H), 1.17 (d, .1: 7.2 Hz, 3H) (inH?Nzo?sz, 489.1154; ”C NMR (101 MHz, CDC13) 5 172.03, found, 168.89,162.33,159.44, 146.66, 143.85, 489.1154 142.75. 141.50. 137.48, 126.75. 126.56, 126.06. 125,43. 12460. 124.55. 109.78. 74.58, 56.28, 47.96, 47.41, 20.76, 18.68, 18.14 ‘H NMR (400 MHz. CD(‘,1~,) 5 8.30 (d, .1 : 7.9 Hz, 1H), 8.26 (d, .1: 5.4 Hz, 1H), 7.214 7.13 H), 7.02 (ddd,J= 3.5, 1.2. 0.6 Hz, 1H). 6.96 4 6.88 (111,411).
HREfZBES', 5.73 (d, .1: 0.7 Hz. 2H). 5.55 (dq_ .1: ([M+H]+) 7.4, 6.2 Hz, 1H), 4.75 4 4,60 (m, 2H), calcd for 3.895(5, 3H), 2.06 (s, 3H), 1.29 (d, .1: 6.3 144 Hz. 3H). 1.19 (d, .14 7.2 Hz. 5H) (721H57N207SZ. 3 #:1111259 ”C N1_V1R (101 MHz, CDC1_3) 5 172.13, 5191258 .162.91,160.26_ 145.69. 143.96. 143.86, 142,81, 142.46. 126.74, 126.55, 126.03, 125.42, 124.58, 124.54, 109.59, 89.52, 74.55, 56.19, 48.18, 47.42, 20.87, 18.70, 17.95 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 5 8.48 — SI 8.37 (m, 1H), 8.30 (d, J: 5.4 Hz, 1H), (m z) 7.29 4 7.18 (m, 4H). 7.05 4 6.90 (m, 5H), (1M4Hr) 5,72 (dq, J : 9,7, 6.2 Hz, 1H), 4.55 (dq, J calcd for = 8.3, 7.2 Hz, 1H), 4.05 (d, J: 9.6 Hz, C27Hl—F3N306. 1H). 3.88 (s. 3H). 2.38 (s, 3H). 1.22 (d. J 5131837; : 6.1 Hz. 3H). 1.00 (d. .1: 7.2 Hz. 3H) found, 513.1835 19F NMR (376 MHz, CDC13) 5 -115.58,-115.93 1H NMR (400 MHz, CDCl;) 5 8.26 (d, J HRMS—ESI = 5.4 Hz, 1H), 8.22 (d, J: 7.8 Hz, 1H), (m 2) 7,32 4 7.16 (m, 4H), 7,05 4 6.89 (m, 5H), (1M4Hr) 5.78 4 5,68 (m, 1H). 5.72 (3,211). 4.64 4 calcd for 4.50 (m, 1H), 4.06 (d, J: 9.7 Hz, 1H), C38H29F3N307, 3.90 (s, 3H), 2.06 (s, 3H), 1.24 (d, J: 6.1 5431943; Hz, 3H). 1.00 (d. .1: 7.2 Hz, 3H) found, 543.1938 19F NMR (376 MHz, CDC13)5 —1 1559—11597 1H NMR (400 MHz.CDC1~,)5 8.34 (d. .1 = 7.9 Hz, 1H), 8.25 (d, J: 5.4 Hz, 1H), 7.39 — 7.16 (m, 10H), 6.94 (d, J: 5.4 Hz, 1H). 5.97 (q, .1: 6.2 Hz, 1H). 5.78 4 5.61 HRMS-ESI (m, 2H), 4.74 4 4.56 (m, 1H), 3.90 (s, (m z) 3H), 3.42 (dq, J: 9.2, 7.0 Hz, 1H), 3.21 ([M4Hr) (dq. J: 9.2. 7.0 Hz. 1H). 2.05 (3.311), calcd for 1.25 (d. .1: 7.2 Hz, 3H), 1.19 (t. .1 : 6.9 C30H35N308, Hz, 3H), 1.12 (d, J: 6.3 Hz, 3H) 551.2393; found. ”C NMR (101 MHz. CD(‘,1~,) 5 172.13. 96 17023,162.87,160.27, 145.64, 144.02, 142.35,142.09,140.72, 128.24, 127.84, 127.81. 127.70, 127.27. , 10957, 89.52, 84.04, 74.08. 59.96, 56.18. 48.26, 2086,1823, 1570,1495 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 8 8.26 (d, J = 5.3 Hz, 1H), 8.22 (d, J: 7.8 Hz, 1H), 7.38 (td. J: 8.6, 6.2 Hz, 1H), 7.24 (td, J HRMS-ESI : 84,63 Hz, 1H), 6.96 (d, J: 5.5 Hz, (777 2) 1H), 6.88 — 6.69 (m, 4H), 5.88 — 5.75 (m, ([M4Hr) 1H), 5.73 (s. 2H), 4.69 (d, .1: 9.8 Hz; calcd for 1H), 4.65 4 4.55 (m, 1H), 3.91 (s. 3H); C28H37F4N307, 2.07 (s, 3H), 1,29 (d, J: 6.2 Hz, 3H), 579.1754; 110 (d,J= 7.2 Hz, 3H) found. 579.1756 ”P NMR (376 MHz, CDC13) 8 -111.11 (d, J: 7.6 Hz), -111.57 (d, J: 75 Hz). —1 1 1.99 (dd, .1: 7.7, 2.6 Hz), — 112.76 (dd. J: 7.6, 2.5 Hz) 1H NMR (400 MHz, CDC13) 8 8.33 (d, J = 7.9 Hz, 1H), 8.25 (d, J: 5.4 Hz, 1H), 7.40 4 7.18 (m, I()H)_6,94(d..1: 5.4 Hz, HRMS-ESI 1H), 5.97 (q, J: 6.2 Hz, 1H),5.814 5.63 (m z) (m, 2H), 4.72 — 4.52 (m, 1H), 3.90 (s, [M—OCHq+ 3H), 3.17 (s. 3H), 2.05 (s, 3H). 1.24 (d. J calcd for : 7.2 Hz. 3H), 1.12 (c1. J: 6.3 Hz. 3H) C28H29N207: 505.1975; ”C NMR (101 MHz, CDC13) 8 , found, 17024, 162.88, 160.27. 145.65. 144.02, 75 142,35,141.39,140.04, 128.50, 128.08, 127.87,127.71,127.45, 127.28, 109.57, 8953,8446, 73.815619525948125; .86, 18.18, 14.98 1H NMR (400 MHz, CDC13) 8 8.39 (d, J = 8.1 Hz, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.37 (td. J: 8.5, 6.1 Hz, 1H), 7.23 (td, J SI : 8,5, 6.2 Hz, 1H), 7.00 (d, J : 5.5 Hz, (777 2) 1H), 6.90 — 6.68 (m, 4H), 5.89 — 5.71 (m, ([M4Hr) 1H), 4.69 (d, J: 9.8 Hz, 1H), 4.62 4 4.51 calcd for (m, 1H). 3.90 (s, 3H). 2.39 (s, 3H)_ 1.28 C27H35F4N206, (d, J: 6.2 Hz, 3H), 1.09 (d, J: 7.2 Hz, 48; 3H) found. 549.1645 ”P NMR (376 MHz, CDC13) 8 -111.11 (d,J=7.7 Hz), -111.55 (d,J= 75 Hz),-112101 (dd, J: 7.7, 2.6 Hz), — 112.80 (dd. J: 7.6, 2.6 Hz) [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) 1H NMR (400 MHz, CDC13) 5 8.38 (d, J HRMS—ESI = 8.2 Hz, 1H), 8.30 (d, J: 5.4 Hz, 1H), (m z) 7.50 2 737 (m, 4H), 7.37 2 7.19 (m, 6H), ([M4Hr) 6.98 (d, J: 5.5 Hz, 1H), 5.98 (dq, J: calcd for 25.1, 6.4 Hz, 1H), 4.63 4 4.54 (m, 1H), C27H13FN306, 3,87 (s, 3H), 2.37 (s, 3H), 1.30 (d, .1: 6.5 495.1931; Hz, 3H). 0.88 (d, .1: 7.2 Hz, 3H) found, 26 19F NMR (376 MHz, CDC13) 5 4168.48 1H NMR (400 MHz, CDCl;) 5 8.26 (d, J = 5.3 Hz, 1H), 8.20 (d, J: 7.7 Hz, 1H), HREiSZ'FSI, 7.49 4 7.40 H), 7,36 4 7.21 (111,611), 6.93 (5,.1: 5.5 Hz, 1H), 5.99 (dq. .1: (1M+HJ+) .2, 6.4 Hz, 1H), 5.71 (s, 2H), 4.68 4 calcd for 153 4.49 (m, 1H), 3.89 (s, 3H), 2.05 (s, 3H), C H‘ W 0 33‘ 3“ ,3 7‘ 1.31 (d,.1: 6.5 Hz, 3H), 0.90 (d, .1: 7.2 Hz 3H) found, ’ 32320” ”P NMR (376 MHz. CDC1~,) 5 -168.67 1H NMR (400 MHz, CDC13) 5 8.42 (d, J = 8.1 Hz, 1H), 8.30 (d, J: 5.4 Hz, 1H), 7.26 4 7.13 (m, 4H), 6.97 (d, .1: 5.5 Hz, 1H), 6.85 4 6.71 (m, 4H), 5.71 (dq, J: HRMS—ESI 9.9, 6.2 Hz, 1H), 4.64 4 4.47 (m, 1H), (m z) 396 (d, .1: 9.8 Hz, 1H), 3.87 (s, 3H), (|M+Hr) 3.74 (s, 3H). 3.72 (s. 3H), 2.38 (s. 3H), calcd for 1.22 (d, J: 6.1 Hz, 3H), 0.98 (d, J: 7.2 155” ' C29H33N208; Hz, 3H) 537.2237; found, ”C NMR (101 MHz, CDC13)8 172,21, 537.2226 168.88,162.28,159.42, 158.33, 158.20, 146.66, 1411.53, 137.43, 133.90, 13382, 129.02, 129.00, 114.09, 113.83. 109.74. 73154, 5626.56.08, 55.19, 47.90, 20.74, 19.22, 18.08 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 8 8.41 (d, J HRMS—ESI = 7.6 Hz, 1H), 8.31 (d, J: 5.5 Hz, 1H), (m z) 7.32 2 7.18 (m. 2H). 7.12 2 6.82 (m. 7H). (1M4Hr) 5.73 (dq, J : 9.7. 6.2 Hz, 1H), 4.64 4 calcd for 4.43 (m, 1H), 4.06 (d, J: 9.8 Hz, 1H), C27H2—F3N30.,. 3.89 (s. 3H). 2.38 (s. 3H). 1.25 (d. .1: 6.2 513.1837; Hz. 3H). 0.99 (d. .1: 7.2 Hz. 3H) found, 513.1833 19F NMR (376 MHz, CDC13) 8 -112.15.-112.56 1H NMR (400 MHz, CDC13)8 8.41 (d, J = 7.7 Hz, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.314 7.10 (m. 8H). 6.99 (d. J: 5.5 Hz. 1H). 5.72 (dq. .1: 9,8. 6.0 Hz. 1H). 4.59 “1137473231351 — 4.50 (m, 1H), 4.01 (d, J: 9.8 Hz, 1H), 3.88 (s, 3H), 2.38 (s, 3H), 1.24 (d, J: 6.1 ([M+H1+) Hz. 3H). 1.00 (d. .1: 7.1 Hz. 3H) calcd for 157 ___ ___ C73331231606 ”C NMR (101 MHz, CDC13) 8 172.10, 7 181111 ‘ 168.87. 162.33. 159.43. 146.68. . 142.44. 141.40. . 134.67. 134.38. 7545 1239" 130.21,129.95,128.46,128.34,128.10, 127.45,127.17,126.23, 126.13, 109.80, 72.61. 56.98. 56.28. 47.82. 20.75. 19.12. 17.98 1H NMR (400 MHz, CDClg) 8 8.26 (d, J : 5.4 Hz. 1H). 8.23 (d. .1: 8.0 Hz. 1H). 7.24 4 7,14 (m. 4H). 6.93 (d. .1 : 5.4 Hz. 1H), 6.85 — 6.75 (m, 4H), 5.77 — 5.68 (m, HRMS—ESI 1H), 5.72 (s, 2H), 4.63 — 4.50 (m, 1H), (m z) 3.97 (d. .1: 9.9 Hz. 1H). 3.89 (s. 3H). (1M4Hr) 3.75 (s, 3H), 3.73 (s, 3H), 2.05 (5,311), calcd for 1.23 (d, J: 6.2 Hz, 3H), 0.99 (d, J: 7.2 (130143501209. HZ 3H) 567.2342; found, 13C NMR (101 MHz, CDC13) 8 172.34, 38 170.24,162.88,160.24, 158.33, 158.20, 145.70. 14391. 142.54. . 133.82. 129.00,114.09,113.83,109.55,89.51, 73.49, 56.17, 56.10, 55.20, 48.12.2085, 19.23. 17.90 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 8 8.26 (d, J = 5.4 Hz, 1H), 8.23 (d, J: 7.9 Hz, 1H), 7.32 4 7.18 H). 7.14 4 7.03 (m, 2H), (£4313 7,04 4 6.80 (m, 5H), 5.82 4 5.67 (m, 1H), .72 (s, 2H), 4.65 4 4.48 (m, 1H), 4.07 (d, calcd for 159 .1: 9.9 Hz, 1H), 3.90 (s. 3H), 2.06 (s, (,7 H71 RN70 72451943 7‘ 3H), 1.26 (d, .1: 6.1 Hz, 3H), 1.00 (d, .1: * ' * 7.2 Hz, 3H) found, 3411941 ”P NMR (376 MHz. CD(‘,1~,) 8 41 12.16, 411259 1H NMR (400 MHz, CDClg) 8 8.26 (d, J : 5.3 Hz. 1H), 8.22 (d, .1: 7.6 Hz. 1H), .33 4 7,10 (m, 8H). 6.94 (d, .1: 5.4 Hz, , 1H), 5.80 4 5,65 (m, 1H), 5.72 (s, 2H), PRFHIYSZ'FSI 4.60 4 4.52 (m, 1H), 4.03 (d, J: 9.8 Hz, 1H), 3.90 (s. 3H), 2.06 (d, .1: 1.8 Hz, (I M+H|+) 3H), 1.26 (d, J: 6.0 Hz, 3H), 1.02 (d, J: calcd for 160 ___ ___ 7.1 Hz 3H) C28H29C12N207, ’ 57f“)? ”C NMR (101 MHz.CDCl¢,)5172.34, 572%,19 170.24,162.88,160.24, 158.33, 158.20, " 145.70,143.91,142.54,1339513382, 129.00, 114.09, 113.83. 109.55. 89,51, 7349, 56.17, 56.10, 55.20, 48.12, 20.85, 19.23, 17.90 HRMs—ESI 1H NMR (400 MHz. CDC1,) 8 8.77 4 (m z) 8.53 (m. 1H), 8.40 4 8.29 (m, 1H). 7.79 4 ([M+H]+) 7.62 (m, 3H), 7.61 4 7.47 (m, 1H), 7,47 4 calcd for 7.34 (m, 2H), 7.34 4 7.20 (m, 2H), 7.05 4 C27H37NZO(,, 6.94 (m. 1H), 5.83 4 5.66 (m, 1H). 4.93 4 475.1869; 477 (m, 1H), 4,37 4 4.21 (m, 1H), 3.89 found, (3, 3H), 2.47 4 2.37 (m, 3H), 1.63 4 1.47 4751865 (111,3H).0.84 4 0.67 (m, 3H) ”1134775231381 1H NMR (400 MHz, 8 8.58 , 8.43 (m, 1H), 8.40 4 8.32 (m, 1H), 7.36 4 ([M+H]+) 7.19 (m. 4H), 7.13 4 7.03 (111,4H), 7.02 4 calcd for 162 6.97 (m. 1H), 5.17 4 5.05 (m, 1H). 4.77 4 C7 H7—N70 4791-18 187? 4.64 (m, 1H), 4.35 4 4.19 (m, 1H), 396 4 161111d 7 3.85 (m, 3H), 2.40 (d, J: 3.6 Hz, 3H). 491.183 1.504 1.41 (111,3H). 1.07 4 0.93 (m, 3H) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) HRMS'ESI 1H NMR (400 MHz, CDC13) 8 8.52 7 (“$214) 837 (m. 1H). 8.32 7 8.24 (m. 1H). 7.80 7 7.63 (m. 3H). 7.61 7 7.47 (m. 1H). 7.45 7 calcd for 163 --- --- 7.22 (m, 4H), 7.01 — 6.92 (m, 1H), 5.83 — C H «N O 36%; 973;? 5.68 (m, 3H), 4.97 7 4.73 (m, 1H), 4.38 7 ‘ 16666“ 4.19 (m. 1H). 3.92 (s. 3H). 2.07 (s. 351). 1.64 71.49(m,3H),0.90 7 0,66 (16,5H) 5051961 HREiSZ'FSI 1H NMR (400 MHz. CDCL.) 5 8.39 7 8.25 (m. 2H). 7.39 7 7.20 (m. 4H). 7.15 7 (1MMy) 7.00 (m, 4H), 6.99 7 6.92 (m, 1H), 5.817 calcd for 164 5.72 (m, 2H), 5.16 7 5.09 (m, 1H), 4.79 7 (.7 END 53213924?“ 4.67 (m. 1H). 4.37 7 4.17 (m. 1H). 3.91 ‘ foHnd * (s, 3H), 2.08 (s, 3H), 1.51 7 1.43 (m, 3H), 1.09 7 0.93 (m, 3H) 521.1913- ‘H NMR (400 MHz. CDCL.) 8 8.39 (d. .1 : 6.8 Hz, 1H), 8,31 (d, J: 5.4 Hz, 1H), 7.45 7 7.31 (m, 4H), 7.18 7 7.06 (m, 4H), 7.00 (d. .1: 55 Hz. 1H). 5.71 (dq, .1: 9.5.6.2 Hz. 1H). 4.65 7 4.46 (m. 1H). ($171314) 4.00 (d, J: 95 Hz, 1H), 3.89 (s, 3H), 2.38 (s, 3H), 1.22 (d, J: 6.2 Hz, 3H), “a C1 d for 165 1.02 (d. .1: 7.2 Hz. 3H) 7BFZN2064 633 .0236; ”C NMR (101 MHz, CDC13) 8 172.05, found, 168.89. 162.33. 159.47. 146.65. 141.39. 633 .0230 39.74. 139.71. 137.49. 131.97. 131.68. 129.89,129.78,121.06, , 109.84, 72.56, 56.41, 56.30, 47.83, 20.76, 19.09, 17.98 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDClg) 8 8.51 (d, J = 8.1 Hz, 1H), 8.32 (d, J: 5.4 Hz, 1H), 6.99 (d. .1: 5.5 Hz. 1H). 6.74 (d. .1: 3.4 Hz, 1H), 6.67 (d, J: 2.6 Hz, 1H), 6.60 4 PRxSZfSI 6.42 (m, 2H), 5.53 4 5.59 (m, 1H), 4.72 4 4.38 (m. 1H). 4.44 (d. .1: 7.1 Hz. 1H).
”WHF) 3.88 (s. 3H). 2.41 4 2.38 (m. 9H). 1.27 (d. calcd for 166 J— 6.2 Hz, 3H), 1.22 (d, J— 7.2 Hz, 3H) Cstngzo?sz, 3 11,3111“ ”C NMR (101 MHz. CDCL.) 8 172.07. 168.90,16233,159.44, 146.66, , 517 1465' “ 141.56,140.54,138.98,138.92,137.47, 125.77. 125.08.124.66. 124.42. 10976. 74.45. 56.28. 48.01. 47.83. 20.75. 18.64. 1821, 15.25 1H NMR (400 MHz, CDC13) 8 8.42 (d, J : 8.0 Hz. 1H). 8.29 (d. .1: 5.4 Hz. 1H). 7.20 4 7.10(111,4H), 7.10 4 6.99 (m, 4H), 6.96 (d, J: 5.5 Hz, 1H), 5.77 (dq, J: HRMs—ESI 10.0. 6.2 Hz. 1H). 4.65 4 4.45 (m. 1H). (m z) 3.98 (d. .1: 10.0 Hz. 1H). 3.85 (s. 3H).
([M+H]+) 2.37 (s, 3H), 2.26 (s, 3H), 2.23 (s, 3H), calcd for 1.23 (d, J: 6.1 Hz, 3H), 0.93 (d, J: 7.1 NZO(,. Hz. 3H) 505.2338; found, ”C NMR (101 MHz, CDC13) 8 172.23, 505.2345 168.90. 162.28.159.42. 146.67. 14158. 138.67, 138.57, 137.44. . 136.02. 129.41,129.11,127.94,127.91,109,74, 7344, 57.06, 56.27, 47.91, 20.97, 2094, .76, 19.26, 17.99 ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 8 8.36 (d, J = 8.8 Hz, 1H), 8.29 (d, J: 5.4 Hz, 1H), 7.19 4 7.12 (111,4H). 7.10 4 6.98 (111,411). 6.94 (d, J: 5.5 Hz, 1H), 5.76 (dq, J: SI 10.0, 6.2 Hz, 1H), 4.60 — 4.45 (m, 1H), (m z) 3.97 (d, .1: 9.9 Hz, 1H), 3.84 (s, 3H), (1M4Hr) 3.00 4 2,85 (m, 1H). 2.26 (s, 3H). 2.24 (s, calcd for 3H), 1.34 (d, J: 7.0 Hz, 6H), 1.22 (d, J: C31H3-N306, 6.1 Hz, 3H), 0.93 (d, J: 7.2 Hz, 3H) 533.2651; found, ”C NMR (101 MHz, CDC13) 8 174,69, 533.2655 ,162.28,159.39, 146.57, 141.98, .138.59,137.60_ 136.31. 13601, 129.40, 129.10, 127.95. 127.93, 109.58, 7340,5705, 5627,4789, 3395,2097, 2094, 19.25, 18.84, 18.04 ‘H NMR (400 MHz. CD(‘,1~,)5 8.26 (d, .1 : 5.4 Hz, 1H), 8.21 (d, J: 7.8 Hz, 1H), 7.45 — 7.33 (m, 4H), 7.22 — 7.03 (111,4H), 6,95 (d, .1: 5.4 Hz, 1H), 5.83 4 5.61 (m, HRMS'ES', 1H), 5.72 (s. 2H), 4.56 (p, .1: 7.3 Hz, ($171314) 1H), 4.01 (d, J: 9.6 Hz, 1H), 3.90 (s, 3H) 2.06 (s, 3H), 1.24 01:1: 6.2 Hz, 621168 for 169 5H), 1.02 (d, .14 7.2 Hz, 3H) (szquBerzoz.
”C NMR (101 MHz, CDC13) 8 172.18, found, 170.25, 162.91, 160.27, 145.69. 143.97, 66303 142.36, 39.81,139,71_131.97_ 131.68, 129.87,129.76,121.06, 120.77, 109.63, 89.49, 72.51, 56.46, 56.20, 48.06, 20.87, 19.12, 17.81 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDClg) 8 8.31 (d, J = 7.9 Hz, 1H), 8.27 (d, J: 5.3 Hz, 1H), 6.94 (d. .1: 5.4 Hz, 1H). 6.75 (d, .1: 3.4 Hz, 1H), 6.70 4 6.62 (m, 1H), 6.57 4 6.50 HRMS—ESI (m, 2H), 5.77 4 5.70 (m, 2H), 5.52 4 5.40 (777 2) (m, 1H), 4,75 2 4.58 (m, 1H), 4.45 (d, J: (119141113 7.1 Hz, 1H)_ 3.90 (s. 3H). 2.40 (d. .1: 1.2 calcd for Hz, 3H), 2.39 (d, J: 1.1 Hz, 3H), 2.06 (s, C36H31N30783, 3H), 1.36 4 1.14 (m, 6H) found, ”C NMR (101 MHz, CDC13)5 172.17, 547.1585 170.25,162.90,160.26, , 143.95, . 141.64. . 138.96. . 125.73, 125.07, 124.65. 124.41. 109.55. 89.54, 74.42, 56.18, 48.23, 47.85, 2087, 1866,1803, 1524 ‘H NMR (400 MHz. CDCL.) 8 8.33 4 8.15 (m, 2H), 7,2 4 7.10 (m, 4H), 7,10 4 6.99 (m, 4H), 6.92 (d, J: 5.4 Hz, 1H), 5844569 (In, 3H).4.55 (11-1: 7.3 Hz.
HRMS'ES', 1H). 3.99 (c1, .1: 10.0 Hz, 1H). 3.87 (s, ($171314) 3H), 2.27 (s, 3H), 2.24 (s, 3H), 2.05 (s, 3H), 1.24 (d, J: 6.2 Hz, 3H), 0.95 (d, J: “?led for 171 7 2 Hz 3H) CmstNzOm ‘ ‘ 5 3312:? ”C NMR (101 MHz, CDC13) 8 172.34, 170.24, 162.87. 160.24. 145.70. 143.90, 535 24419 142.59, 138,70. 138.58. 136.32. 135.99. 129.40,129.10,127.93, 127.90, 109.55, 89.51, 73.38, 57.07, 56.17, 48.12, 20.96, .93, 20.86. 19.26, 17.81 1H NMR (300 MHz, CDC13)8 8.42 (d, J HRMS—ESI = 7.7 Hz, 1H), 8.31 (d, J: 5.4 Hz, 1H), (m 2) 7,60 , 7‘50 (m, 2H), 7,47 2 7.37 (m. 2H). (119141113 7.34 4 7,13 (m, 5H). 6.99 (d. .1 : 5.4 Hz. calcd for 1H), 5.83 (dq, J: 9.6, 6.2 Hz, 1H), 4,65 C38H38F3N306, 4 4.45 (m, 1H), 4.14 (d, J: 9.7 Hz, 1H), 5451899; 3.88 (s, 3H). 2.38 (s. 3H). 1.25 (d. .1: 6.2 found, Hz, 3H), 0.92 (d, .1: 7.2 Hz, 3H) 545.1902 ”F NMR (376 MHz. CDCL.) 8 -62.56 ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (300 MHz, CDClg) 5 8.40 (d, J = 8.1 Hz, 1H), 8.30 (d, J: 5.5 Hz, 1H), 7.314 7.12 (m, 8H). 6.99 (d, J: 5.5 Hz, HRMS-ESI 1H), 5.72 (dq, J: 9.5, 6.1 Hz, 1H), 466 (m z) 4 4.47 (m, 1H), 4.03 (d, J: 9.5 Hz, 1H), ([M4Hr) 3.88 (s,31—1)_ 2.38 (s, 3H), 1.22 (d, .1: 6.1 calcd for Hz, 3H). 1.01 (d, J: 7.1 Hz, 3H) C27H27C12N2065 545.1246; ”C NMR (75 MHz, CDC13) 5 172.06, found, , 162.33, 159.45. 146.66. 141.36, 545.1244 139,32,13927,137.47, 132.94, 132.69, 129.51,129.41,129.01,128.72,109.85, 72.70, 56.30, 56.27. 47.83, 20.75, 19.09, 17.98 1H NMR (300 MHz, CDC13) 5 8.26 (d, J = 5.4 Hz, 1H), 8.22 (d, J: 7.8 Hz, 1H), HRS/7178;“, 7.58 4 7.49 (m, 2H). 7.42 (d, J : 8.2 Hz, 2H), 7.35_4 7,12 (m, 5H), 6.95 (d, J : 5.4 ([M+H]+) _ calcd for Hz, 1H), 5.84 (dq, J: 9.8, 6.2 Hz, 1H_), 175 5,72 (s, 2H). 4.62 4 448 (m, 1H). 415 (d, OH RN70 [8575112005 7‘ J: 9.8 Hz. 1H), 3.90 (s. 3H), 2,06 (s, " “ 3H), 1.26 (d,J= 6.1 Hz, 3H), 0.93 (d,J= found, 7 2 Hz 3H) 575.201 1 ‘ ’ ”P NMR (376 MHz, CDC13)8 -62.57 1H NMR (300 MHz, CDClg) 5 8.26 (d, J : 5.4 Hz. 1H), 8.22 (d, J: 7.8 Hz, 1H), 7.34 4 7,09 (m, 8H). 6.95 (d, J : 5.4 Hz, SI 1H), 5.81 4 5.58 (m, 3H), 4.67 4 4.44 (m, (m z) 1H), 4.04 (d, J: 9.5 Hz, 1H), 3.90 (s, (|M+Hr) 3H), 2.06 (s. 3H), 1.24 (d, J: 6.2 Hz, calcd for 3H), 1.02 (d, J: 7.1 Hz, 3H) C28H29C12N207: 575.1352; 13C NMR (75 MHz,CDC1~,)5 172.19, found, 170.28, 162.91, l6(),27_ 145.71. 143.95, 575.1352 142.32,139.38,139.28, , 132.67, 129.49, 129.40, 129.01, 128.71, 109.64, 89.47, ?2.65, 56.32, 5622, 56.18. 48.05, 2089, 20.86, 19,12,1781 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. ()0 (cm'l) (H, ”C, 191:) (Thin 3387, 2984, 1737, 1H NMR (400 MHz, CDC13) 5 8.35 (dd, J 1673, : 4.5, 1.3 Hz, 1H), 8. 15 (d, J: 78 Hz, 1603, SI 1H), 7.52 (dd, .1: 8,4, 1.4 Hz, 1H), 7.42 1579, (m z) (dd, J: 84,45 Hz, 1H), 7.33 — 7.14 (m, 1506, ([M+H]+) 4H), 7.05 — 6.86 (m, 4H), 5.82 (s, 2H), 1451, calcd for 5.72 (dq, .1 : 9.7, 6.1 Hz, 1H), 459 (p, .1 1368, C27H17F3N206, : 73 Hz, 1H), 4.06 (d, J: 9.7 Hz, 1H), 1304, 5131832, 2.11 (s, 3H), 1.24 (d, J: 6.2 Hz, 3H), 1268, found, 101 (d, .1: 72 Hz, 3H) 1199, 5131833 1159, 1”F NMR (376 MHz, CDC13) 5 1136, -115.57,-115.97 1045, 1007, 969, 825, 779, (Thin 3380, 2985, 1737, 1674, 1603, 1H NMR (400 MHz, CDC];) 5 8.23 (d, J 1578, : 5.3 Hz, 1H), 8.18 (d, .1: 7.8 Hz, 1H), HRMS'ESI 1507, 7.23 (ddd, J: 13.9, 6.9, 2.6 Hz, 4H), 1473, 314) 705 — 6.84 (111,5H), 5.78 — 5.66 (m, 3H), 1455, 4.56 (p, .1: 7.3 Hz, 1H), 4. 12 (q, .1: 7.0 calcd for 179 1366, Hz, 2H), 4.05 (d,J: 9.7 Hz, 1H), 2,06 (s, C H F N 0 1312, 22531289; 7’ 3H), 1.47 (t, J: 7.0 Hz, 3H), 1.24 (d,J= 1274, * ' ' ‘ 62 Hz, 3H), 1.00 (d, .1: 7.2 Hz, 3H) found. 1222* 557 2089 1200, ~ ' ' 1”F NMR (376 MHz, CDC13) 5 1158, -115.60,-115.98 1 104, 1043, 1003, 968, 910, 886, 824, 792, [Annotation] Mel.Chan None set by Mel.Chan ation] an MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) (Thin 3404, 2983, 1737, 1652, 1 H NMR (400 MHz, CD(,1~.) 5 8. 13 (dd, .1, , , 1508‘ :79, 1.8 Hz, 1H), 8.06 (d,J:6.9 Hz, 1482’ SI 1H), 7.45 (ddd, J: 8.5, 7.4, 1.8 Hz, 1H), 1453, (777 2) 7,29 2 7.05 (m, 6H), 7.04 2 6.90 (m, 4H), 1369‘ (| M4Hr) 5.92 (d, .1: 6.4 Hz, 1H), 5.83 (d. .1: 6.4 calcd for Hz, 1H), 5.73 (dq, J: 9.9, 6.2 Hz, 1H), 180 1305’ 1222’ CstngzNo?, 4.57 (p, J: 7.1 Hz, 1H), 4.06 (d, J: 9.7 512.1879; Hz, 1H), 2.14 (s, 3H), 1.25 (d, .1: 6.0 Hz, 1 197‘ _ found, 3H), 1,00 (d, J: 7.2 Hz, 3H) 1159, 512.1889 ’ 19 F NMR (376 MHz, CDC1~,) 5 41562 —11601 1088, ‘ ~ ~ ~ 1049, 1010, 976, 91 1, 828, 792, 759, ‘H NMR (400 MHz, CD(‘,1~,)5 8.24 (t, .1 : 77 Hz, 2H), 7.57 4 7.49 (m, 8H), 7,45 — 7.37 (m, 8H), 7.32 (dt, J: 9.3, 5.8 Hz, 2H), 6.90 (d, .1: 5.4 Hz, 1H), 5.89 (dq, J HRMS-ESI : 12.4, 6.1 Hz, 1H), 5.71 (s, 2H). 4.58 (p, (m z) J: 7.3 Hz, 1H),4.16 (d,J= 10.0 Hz, ([M+H]+) 1H), 3.88 (s, 3H), 2.05 (s, 3H), 1.33 (d, J calcd for : 6.1 Hz, 3H), 0.96 (d, .1: 7.2 Hz. 3H) C411H39N2073 659.2752; ”C NMR (101 MHz, CDC13) 5 172.38, found, 170.26, 162.88, 160.23, 145.68, 14394, 6592758 142.52, 140.73, 140.61. 140.52. 140.23, 139.89,139.63,128.74,128.71,128,55, 12755, 127.26, 127.17, 126.99, 12696, 109.50, 89.54, 73.27, 57.25, 56.15, 48.12, 20187, 19.34, 17.79 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd. MP IR NMR “L133, No. (0C) anrb CH,”C_”F) IHNMRomOMMLCDC9584u¢J =51H;1H1&%M¢J=54HL1H1 7577747mL8Hy74ldeé93.60 1u.&41732(dd21:121,111u,311 694(d“]=55]?;11D,588(dq¢]= In?deSI/ 123.61H11H1457@“P:72HL (W??f) 1HL4U(dJ:HMHt.Hu387@ ?DJ38®3HL1M1¢J=61Hz mkdbr 1& u- u— ¢J=11H;J? QJkN?m 612L316; ”C NMR (101 MHZ, CDC13)8 17224. 6292651 16229,15940,14663.14152 ' ' 14062.140A7_14023.13988. 13962.13745.12875_12871.12856. 12725,12716,12700,12696, 10969,7330,5722,5625,4790,2075, m3Ln97 ‘HNmemOMHLCDcmsgzng =54HL1H1815¢J:56H21H1 7257?15m14ny7037689m15Hy 5757566mL3H141lde:181 57H21H14mu¢J=91HL1H1 , 392(&3}D,389(dd¢l=183.5411; I??gifSI 1H121M(g3H1124¢1J:621u. (1M+H1+> C ‘31:? $0 13C NMR (126 MHZ. CDC1~,) 5 170.32. ’gnéléli “ 16911.16172(d”1:246()Hz)16162 Zb'nde (d“1==245.4I{z),160.31,145.73, -?u ’ 1M0213211%67@WEQ6ZHA 5301809 129.72. 129.66. 1 15.68 (d. .1: 21.5 Hz). 11541 (d, J: 22.1 Hz), 109.65, 89148., 73.37, 56.16, 55.69, 41.33, 20.87 wFNMRQ?lMHzCDGQé -115.60 (111), -115.94 (111) [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (500 MHz, CDC13) 5 8.26 (d, J = 5.4 Hz, 1H), 8.22 (d, J: 8.4 Hz, 1H), 7.28 4 7.18 (m. 4H). 7.01 4 6.90 (m. 5H). .77 4 5.65 (m, 3H), 4.56 (ddd, J: 8.4, 6.7, 5.3 Hz, 1H), 4.05 (d, .1: 9.6 Hz, 1H), 391 (s, 3H). 2.06 (s. 3H). 1.63 4 1.52 (m. 1H). 1.40 4 1.29 (m. 1H). 1.23 (61.7: 6.2 ”11374735381 Hz, 3H), 0.61 (t, J = 7.4 Hz, 3H) (3:111); ”C NMR (126 MHz. CD(‘,1~,)5 171.56. 184 170.27,163.06,161.72(d,J:246.0 Hz), C H F N 0 225;;12312; 7’ 161.66 (d,J= 2452 Hz), 160.32, 145.66, ”10116d ‘ 144.03. 142.38. 136.92. 129.60 (d. .1: .6 Hz). 129.54 (d. .1: 10.4 Hz). 115.63 “558 2133' (d,J=35.4 Hz), 115.46 5.4 Hz), 109.55, 89.59, 73.22, 56.19, 56.02, 55.26, .24. 20.87. 19.22, 9.16 19F NMR (471 MHz, CDC13)8 4115.59 4 41 15.70 (m). 41 16.06 (ddd. .1: 14.0. 8.7. 5.3 Hz) 1H NMR (500 MHz, CDC13) 5 8.29 4 8.21 (m, 2H), 7.29 4 7.14 (m, 4H), 7.00 4 6.88 (m. 5H). 5.85 4 5.51 (m. 3H). 4.55 (dd, J: 9.3, 4.6 Hz, 1H), 4.05 (d, J: 9.6 Hz, 1H), 3.91 (s, 3H), 2.06 (s, 3H), 1.87 4 1.75 (m. 1H). 1.22 (d. .1: 6.2 Hz. 3H). 0.78 (d. .1 : 6.9 Hz. 3H). 0.58 (d. .1: 6.8 HRMS-ESI Hz, 3H) (777 z) (3:111); ”C NMR (126 MHz. CD(‘,1~,) 5 171.17. 185 170.27, 163.21, 161.70 (d,J:246.1 Hz), C H~~F7N 0 ; 7’ 161.66 (d, J: 2453 Hz), 160.38, 145.62, * fo11nd‘ ‘ 144.11. 142.32. ; 129.54.429.54 (4.1: 14.9 Hz). 1 15.6.» (d. .1: 32.3 Hz). 572.2286 115.46 (d, J: 32.3 Hz), 109.54, 89.63, 7325,5714, 597, 3109,2088, 1927. 19.10. 17.06 19F NMR (471 MHz, CDClg) 5 -115.69(ddd..l: 13888.55 Hz). 41 16.12 (5615.7: 138. 8.7. 5.5 Hz) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 19F) 1H NMR (500 MHz, CDC13) 5 8.25 (d, J = 5.4 Hz, 1H), 8.07 (d, J: 8.8 Hz, 1H), 7.28 4 718011.411). 7.01 4 6.91 (m. 5H). .74 4 5.66 (m. 3H), 4.57 (ddd, J: 9.6, 8.7, 5.1 Hz, 1H), 4.04 (d,J= 9.9 Hz, 1H), 3.90 (s. 3H). 2.06 (s. 3H). 1.41 4 1.31 (m. 1H). 1.23 (d..1:6.1 Hz. 3H). 1.224 1.17 y (m, 1H), 1.04 — 0.96 (m, 1H), 0.79 (d, J: HREVHIYSZ'FSI 6.5 Hz, 3H), 0.74 (d, J: 6.6 Hz, 3H) ); ”C NMR (126 MHz, CDC13) 5 172.38, 186 170.29, 163.06, 161.73 (d, J: 245.7 Hz), C H _F N 0 28:92:10; 7’ 161.67 (d. .1: 2454 Hz). . 145.57. 7 161115 ‘ 144.14. 142,22. 13717. . 129.57 (d,J= 12.1Hz), 129.50 (d,J= 11.8 Hz), 58; 2409" 115.64(d,J=35.1Hz),115.47(d,J= .0 Hz). 109.55. 89.60. 73.08.5620. 56.19, 50.69, 41.20, 24.56, 22.80, 21.63, .87, 19.19 ”P NMR (471 MHz.CDC1~.)5 -115.66 (td,J= 9.1, 4.7 Hz), -116.21 (ddd,J= 13.9, 8.7, 5.3 Hz) ‘H NMR (500 MHz. CDCL.) 5 8.38 4 8.23 (m, 2H), 7.27 4 7.12 (m, 4H), 7.10 4 6.83 (m, 5H), 5.69 (dq, J: 9.1, 6.2 Hz, 1H). 4.13 4 3.95 (m. 2H). 3.92 (s. 4H). .39 (s. 3H). 1.23 (61.1 : 6.2 Hz. 3H) HRMS—ESI (m 2) ”C NMR (126 MHz, CDC13) 5 168.98, (|M+H|+) 168.92. . 161.71 (d../:245,8 Hz). calcd for 16162 (d, J: 245.4 Hz), 159.51, 146.67, C26H35F3N306, 141.23, 137.55, 136.79, 136.53 (d,J= 499.1675; 3.4 Hz). 12972 (d. .1: 2.9 Hz). 129.65 found. (d. .1 : 2.7 Hz). 1 1567 (d. .1: 21.3 Hz). 499.1664 115.40 (d, J: 21.3 Hz), 109.89, 73.42, 56.31, 55.71, 41.17, 20.73.1911 ”P NMR (471 MHz, CDC13) 5 -115.55 4 -115.66 (m), -115.95 (rt, .1: 8.3. 4.0 Hz) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) 1H NMR (500 MHz, CDC13) 5 8.39 (s, 1H), 8.32 (d, J: 5.5 Hz, 1H), 7.33 4 7.04 (m, 4H), 7.06 4 6.86 (m, 5H), 5.70 (dq, J : 9,4, 6.1 Hz, 1H), 4.54 (ddd, J: 8,6, 6.5, 5.4 Hz, 1H), 4.04 (d, J: 9.4 Hz, 1H), 3,91 (s, 3H), 2.38 (s, 3H), 1.62 4 1.49 (m, 1H), 1.40 4 1.30 (m, 1H), 1.22 (d, .1: 6.1 “1157475231351 Hz, 3H), 0.59 (t, J: 7.4 Hz, 3H) (321C112); ”C NMR (126 MHz, CD(‘,1~,)5 171.41, 188 168.90, 162.46, 161.71 (d,J:245.9 Hz), C H F N 0 22279198; 6’ 161.66 (d,J= 245.4 Hz), 159.46, 146.63, ' foHnd ‘ 141.46, 137.48, 136.88, 129.63 (d, .1: 7.8 Hz), 129.53 (d, .1: 7.8 Hz), 115.67 '527 1981' (d,J=21.3Hz),115.40(d,J=21.1Hz), 109.74, 73.25, 56.30, 55.96, 53.02, 25.54, .76, 19.20, 9.04 19F NMR (471 MHz, CDC13) 5 4115.62 4 41 15.72 (m), 41 16.07 (td, .1: 9.3, 8.9, 4.1 Hz). 1H NMR (500 MHz, CDC13) 5 8.35 (s, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.35 4 7.16 (m, 4H), 7.08 4 6.80 (m, 5H), 5.70 (dq, .1 : 9,5, 6.1 Hz, 1H), 4.51 (dd, .1: 9.5, 47 Hz, 1H), 4.04 (d,J= 9.5 Hz, 1H), 3.91 (s, 3H), 2.38 (s, 3H), 1.89 4 1.68 (m, 1H), 1.21 (d, .1: 6.3 Hz, 3H), 0.76 (d, .1: 6.9 SI Hz, 3H), 0.58 (d, J: 6.9 Hz, 3H) (777 z) (|M+H|+) ”C NMR (126 MHz, CDCL.) 5 , calcd for , , 161.69 (d, J: 245.9 Hz), C29H31F3N206, 161.65 (d, J: 244.8 Hz), 159.46, 146.61, 541.2145, 1415413748, 13697 (d, 7:33 Hz), found, 136.88 (d, .1: 3.4 Hz), 129.65 (d, .1: 7.9 541.2143 Hz), 129.52 (d,J= 8.0 Hz), 115.66 (d,J = 21.3 Hz),115,41(d,J= 21.3 Hz), 109.71, 73.25, 56.95, 56.30, 55.91, 20.77, 19.25, 18.99, 17.09 19F NMR (471 MHz, CDC1~,) 5 4115.67 4 4115.78(m), -116.06 4 -116.17 (In) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (500 MHz, CDC13) 8 8.30 (d, J = 5.5 Hz, 1H), 8.18 (d, J: 8.2 Hz, 1H), 7.35 4 7.13 (m, 4H). 7.04 4 6.80 (m, 5H), .68 (dq, J : 9.8, 6.2 Hz, 1H), 4.54 (td, J = 9.2, 5.2 Hz, 1H), 4.03 (d, J: 9.7 Hz, 1H), 3.90 (s. 3H), 2.38 (s, 3H). 1.20 (dd, .1: 16.3. 6.1 Hz, 4H). 1.04 (ddd. .1: 13.9, 8.7, 5.2 Hz, 1H),0.914 0.81 (m, HRMS—ESI 1H), 0.78 (d, J: 6.4 Hz, 3H), 0.73 (d, J: (m z) 6.6 Hz, 3H) (lM+HJ+) calcd for ”C NMR (126 MHz, CDC13) 8 172.20, NZOG, 168.87, 162.46, 161.7] (d, .1: 2457 Hz), 555.2301; 161.66 (d. .1: 245.4 Hz), 159.46. , found, 141.50, 137.48, 137.07 (d,J= 3.3 Hz), 555.2292 13689 (d, J: 3.3 Hz), 12960 (d, J: 8.0 Hz), 129.50 (d,.1: 8.0 Hz), 11568 (d,./ : 21.3 Hz), 115.40 (d, J: 21.3 Hz), 109.71, 73.08, 56.23, 50.54, 24.54, 22.76, 21.71,20.76,19.16 1”F NMR (471 MHz, CDC13) 5 415.59 4 -115.77 (111), -116.14 4 41 16.29 (111) (11m 1H NMR (300 MHz, CDC13)8 8.32 4 ?lm) HRMS—ESI 8.19 (m, 2H), 7.47 (dd, J: 7.7, 1.8 Hz, 338]. (m z) 1H), 7.23 (s. 1H), 7.24 4 7.04 (m, 2H), 2937, (| M+Hr) 6.93 (d, .1 : 5.5 Hz, 1H), 6.93 4 6.77 (m, 1735, calcd for 3H), 6.78 (dd, J: 8.3, 1.2 Hz, 1H), 5.95 1676, C30H35N309, (dq, J: 9.9, 6.2 Hz, 1H), 5.78 4 5.66 (m, 1492, 5672335; 2H), 5.01 (d, .1: 9.8 Hz, 1H), 4.62 4 4.48 1245, found, (m, 1H), 3.90 (s, 3H), 3.85 (3,311), 3.76 1203, 567.2337 (3, 3H), 2.06 (s, 3H), 1.24 (d, J: 6.2 Hz, 1042 3H), 0.95 (d, .1: 7.2 Hz, 3H) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 19F) 1H NMR (300 MHz. CDC13) 8 8.27 (d, J (Thin = 5.4 Hz. 1H), 8.23 (d. J: 7.8 Hz. 1H), HRMS-ESI 7.26 4 7.14 (m. 1H). 7.16 (LJ: 7.9 Hz. 2938‘ (m 2) 1H). 6.93 (d, J: 5.4 Hz, 1H), 6.92 4 6.87 1737’ ([M+H]+) (m, 2H), 6.87 — 6.80 (m. 2H), 6.73 (ddd, 1675, calcd for J: 8.2. 2.6. 0.9 Hz. 11-1). 6.69 (ddd. J: 192 ___ 1583‘ (T;UH~.5N30«,. 8.2. 2.6. 0.9 Hz. 1H). 5.79 (dq. J: 9.7. 1%04’ 567.2341; 5.8 Hz, 1H). 5.73 — 5.69 (m, 2H).4.71— 1488, found, 444 (m. 1H), 3.99 (d. J: 10.2 Hz. 1H), 1202‘ 567.2337 3.90 (s. 3H). 3.77 (s. 3H). 3.76 (s. 3H). 1041‘ 2.06 (s, 3H), 1.25 (d, J: 6.1Hz,3H), 0.94 (d, J: 7.2 Hz, 3H) (Thin 1H NMR (400 MHz. CDC1~.) 5 8.24 (dt. J ?lm) HRMS-ESI : 5.4. 1.3 Hz. 1H). 7.99 (d../: 8.1 Hz. 3378, (m 2) 1H), 7.81 (t. J: 8.5 Hz. 1H), 7.36 (t, J: 2983, ([M+H]+) 8.5 Hz, 1H), 7.19 — 7.10 (m, 1H). 7.07 — 1741. calcd for 6.98 (m. 1H). 6.99 4 6.86 (m. 3H). 6.14 4 193 ___ 7 1672, C28H37C13F3N208, 6.04 (m, 1H), 5.70 (d. J: 6.4 Hz. 1H), 1575, 02; 5.64 (d. J: 6.4 Hz. 1H). 4.66 (p. J: 7.2 1483. found. Hz. 1H). 3.92 (s. 3H). 3.82 (s. 1H). 2.07 1201. 627.1107 (5. 3H). 1.35 (d. J: 7.2 Hz. 3H). 1.22 (d. 1002 J: 6.9 Hz. 3H) 1H NMR (300 MHz. CDC13) 5 8.27 (d, J : 5.4 Hz. 1H). 8.23 (d. J: 7.8 Hz. 1H).
(Thin HRMS-ESI 7.15 4 7.02 (m, 2H), 7.00 4 6.84 (m, SH), (m z) 5.76 — 5.63 (m, 3H). 4.66 — 4.49 (m, 11-1), ([M+H]+ 2984’ ) 3.97 (d. J: 9.8 Hz. 1H). 3.91 (s. 3H). calcd for 2.20 (d. J: 1.9 Hz. 3H). 2.18 (d.J: 1.8 ___ 1738‘ 1675) F3N307, Hz, 3H), 2.06 (s, 3H). 1.24 (d, J: 6.2 Hz, ”04’ 571.2257; 3H), 1.02 (d, J: 7.2 Hz, 3H) 120 1‘ _f0L111d._ w 1003‘ 571.225 F NMR (471 MHz, CDC13)OA -116.63 (t.J= 9.5 Hz). -117.12 (t. J: 9.5 (Thin HRMS-ESI 1 . A ?lm) H_NMR (300 MHZ, CDClg) 0 8.27 (d, J (m z) = 5.4 Hz. 1H), 8.23 (d. J: 7.9 Hz. 1H), 3377 + 2983’ ([M+H] ) 7.25 4 7.20 (m. 2H). 7.17 4 7.02 (m. 4H). calcd for 6.94 (d. J: 5.4 Hz. 1H). 5.75 4 5.62 (m. ___ 173; ' 1675) C30H33C13N207, 3H), 4.68 — 4.50 (m. 1H), 3.95 (d. J: 9.9 ”01’ 603.1657; Hz, 1H). 3.91(s, 3H). 2.31 (s, 3H), 2.28 17202‘ found. (5. 3H). 2.06 (s. 3H). 1.24 (d. J: 6.1 Hz. 1050‘ 603.1659 3H). 1.03 (d, J: 7.2 112,311) [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) $1131 1H NMR (400 MHz. CDC13) 8 8.26 (d, J HRMs—ESI : 5.4 Hz. 1H). 8.13 (d. .1: 8.1 Hz. 1H). 587‘ (m z) 7.85 (11.7: 7.6. 1.9 Hz. 1H). 7.47 (11. .1: 1741’ ([M+H] ) 7.7, 1.8 Hz, 1H), 7.28 4 7.20 (m, 1H), calcd for 7.22 — 7.11 (m, 2H), 7.09 — 6.99 (m, 11-1), ___ 16733 1507 szHwFZNZOX. 7.01 4 6.79 (m. 3H). 6.29 4 6.20 (m. 1H). 1486‘ 559.1884; 5.71 (d,J:6.4 Hz, 1H),5.67(d,J:6.4 1453’ found, Hz, 1H), 4.75 4 4.57 (m, 1H), 3.91 (s, 1203’ 559.1886 3H). 3.48 (d. .1: 6.1 Hz. 1H). 2.07 (s. 3H). 1.34 4 1.21 (111.6H) (Thin 3379. SI 1H NMR (300 MHz. CDCL.) 8 8.27 (d. .1 3282, (m z) = 5.4 Hz, 1H), 8.21 (c1, J: 7.8 Hz, 1H), 2984, ([M+H]+) 7.46 4 7.34 (m, 5H), 7.26 4 7.15 (111,311), 2107. calcd for 6.94 (d. .1: 5.4 Hz. 1H). 5.87 4 5.68 (m. 1738, C33H31N207, 3H), 4.62 4 4.48 (m, 1H), 4.07 (d, J : 9.8 1674, 555.2125, Hz, 1H), 3.91 (s, 3H), 3.05 (s, 1H). 3.03 1503. found. (5. 1H). 2.06 (s. 3H). 1.34 4 1.22 (111.3H). 1202. 555.2126 0.98 (d. .1: 7.2 Hz. 3H) 1043, ($11111 1H NMR (300 MHz. CDCL.) 5 8.27 (d, .1 33219) HRMS E81 2') = 5.4 Hz, 1H), 8.23 (c1, J: 7.8 Hz, 1H), 2964’ 7.24 4 7.18 (111,4H), 7.14 4 7.03 (m, 5H), ([M+H1+) 1736‘ 6.93 (d. .1: 5.5 Hz. 1H). 5.87 4 5.69 (m. calcd for 198 16‘75‘ 3H), 4.53 (p, J: 7.3 Hz, 1H), 3.99 (d, J: C37H~9N707 ”05’ 53" 10.1Hz, 1H), 3.90 (d,J= 1.0 Hz, 3H), 1202’ ‘ 1611116 ‘ 2.68 4 2.48 (m. 4H). 2.06 ((1.7: 1.1 Hz. 1042‘ 3H). 1.24 ((17:71 Hz. 3H). 1.224 1.10 563 2722 1003’ ‘ ' “ (m, 6H), 0.88 (d, J: 7.2 Hz, 2H) [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 8 8.27 (d, J = 5.3 Hz, 1H), 8.21 (d, J: 7.9 Hz, 1H), 7.31 4 7.22 (m. 5H). 7.21 4 7.12 (m. 1H). 7.00 4 6.81 (m,3H),5.814 5.74 (m, 1H), HRMS—ESI 5.72 (d, J: 0.8 Hz, 2H), 4.54 (p, J: 7.2 (m z) Hz. 1H). 4.05 (d. J: 9.9 Hz. 1H), 3.90 (s. (119141117) 3H). 2.06 (s. 3H). 1,24 (d. .1 : 6.2 Hz. calcd for 3H), 0.92 (d, J: 7.2 Hz, 3H) 199 ___ ___ CZ8H3UFNZO7: 525.2032; ”C NMR (126 MHz. ~,)5 . found, 17028, 162.87, 161.70 (d, J: 245.6 Hz), 525.2045 160.25,145.69,143.97, 142.50, 141.20, 137.03 (d, .1: 3.3 Hz), 129.60 (d, .1: 7.8 Hz). 128.59. 128.02. 126.80. 11560 (d. .1 = 21.3 Hz), 109.52, 89.55, 73.11, 5704, 56.18, 48.05, 20.87, 19.18, 17.74 ‘H NMR (400 MHz. CD(‘,1~,)5 8.26 (d. .1 : 5.4 Hz, 1H), 7.89 (d, J: 8.0 Hz, 1H), 7.56 (d, J: 2.2 Hz, 1H), 7.48 (d, J: 2.2 Hz. 1H). 7.34 (dd. .7: 8.5. 4.2 Hz. 2H). 7.18(ddd_.1: 10.5. 8.4. 2.2 Hz. 2H). 6.97 (d, J: 54 Hz, 1H), 5.79 (q, J: 6.3 Hz, 1H), 5.68 (d,J= 6.3 Hz, 1H), 5.61 ESIMS (d. .1: 6.4 Hz. 1H). 4.63 4 4.52 (m. 1H). m z 661.1 3.92 (s, 3H), 3.55 (s, 1H), 2.07 (s, 3H), ([M+H]+) 1.27 (d, J: 7.2 Hz, 3H), 1.18 (d, J: 6.3 Hz. 3H) 13C NMR (126 MHz, e-(1’6) 5 166.30,165.13,158.33,155.10,140.60, 39.16. 138.49. 137.43. 137.10. 127.58. 126.60,126.48,125.21, 123.17, 122.62, 119.99, 119.77, 104.55, 84.15, 73.35, 69.04. 51.05. 43.24. 26.40. 15.69920 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NIVIR N0. (‘0 (cm'l) (1H, 13C. 191:) 1H NMR (400 MHz, CDC13) 8 8.26 (d, J = 5.4 Hz, 1H), 7.91 (d, J: 8.0 Hz, 1H), .33 4 7.27 (m. 3H). 7.21 (dd. .1: 10.4. 2.1 Hz, 1H), 7.11 (ddd, J: 8.5, 2.2, 0.8 Hz, 1H), 7.06 (ddd,J= 8.6, 2.1, 0.9 Hz, 1H). 6.97 (d. .1: 5.4 Hz. 1H). 5.80 (q. .1: 6.3 Hz. 1H). 5.68 (d. .1: 6.3 Hz. 1H). .61 (d, J: 6.3 Hz, 1H), 4.63 — 4.51 (m, 1H), 3.92 (s, 3H), 3.54 (s, 1H), 2.07 (s, 3H). 1.25 (d. .1: 7.2 Hz. 3H). 1.18 (61.7: ESIMS 6.4 Hz, 3H) 202 m/Z 627.1 (WT) 13C NMR (126 MHz. CDC1~,) 8 171.43. 170.32. 163.50. 160.30. 157.99 (d. .1: 249.5 Hz), 157.96 (d, J: 249.3 Hz), 145.76, 145.20 (d, J: 5.8 Hz), 143.73, 143.09 (d. .1: 6.1 Hz). 142.58. 13053 (d.
J: 3.2 Hz), 122.14 (d, J: 3.8 Hz), 121.85 (d,J= 3.5 Hz), 120.23 (d,J= 17.8 Hz). 120.05 (61.1: 17.8 Hz). 114.70 (d. .1 : 22.5 Hz). 114.34 (d. .1: 23.0 Hz). 109.72, 89.34, 78.60, 74.30, 56.24, 48.39, .94, 20.86, 443 ‘H NMR (400 MHz. CDC1,) 8 8.27 (d. .1 : 5.4 Hz, 1H), 8.21 (d, J: 7.8 Hz, 1H), 7.26 — 7.19 (m, 2H), 7.10 (dd,J= 8.5, 2.2 Hz. 2H). 7.03 (ddd. .1: 13.4. 8.2. 2.3 Hz. 2H). 6.94 (d. .1: 5.5 Hz. 1H). 5.77 4 5.62 HRMS-ESI (m, 3H), 4.56 (p, J: 7.2 Hz, 1H), 3.95 (m z) (d,J= 10.0 Hz, 1H), 3.91 (s, 3H), 2.33 (I M+H l+) (s. 3H). 2.31 (s. 3H). 2.06 (s. 3H). 1.23 calcd for (d, J : 6.1 Hz, 3H), 1.00 (d, J : 7.2 Hz, C30H33C12N207, 3H) 603. 1 659; found. ”C NMR (126 MHz. CD07.) 8 172.30. 603. 1666 170.28,162.90,160.27, 145.70, 143.97, 142.42,139.64,139.47, 136.51, 136.11, 133.06. 13271. 130.74. . 129.42. , 126.63, 126.49, 109.57, 89.52, 72.78, 56.44, 56.19, 48.06, 20.87, 20.17, .09. 19.19 17.82 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 8 8.40 (d, J = 7.9 Hz, 1H), 8.32 (d, J: 5.5 Hz, 1H), 7.30 4 7.22 (m, 6H). 7.19 4 7.13 (m, 1H), 7,014 6.93 (m, 3H), 5.76 (dq, J: 9,8, 6,2 HRMS—ESI Hz, 1H), 4.58 4 4.49 (m, 1H), 4.05 (d,J= (m z) 9.9 Hz, 1H), 3.90 (s. 3H), 2.38 (s. 3H), (1M4Hr) 1.23 (d, .1: 6.1 Hz, 3H), 0.90 (d. .1: 7.2 calcd for Hz, 3H) 204 "_ --_ CZ7H2‘FNZO6: 495.1926; ”C NMR (126 MHz, CD(‘,1~,)5 172.19, found, 168.90, 162.27, 161.69 (d, J: 245.6 Hz), 159.42,146.64,141.51,141.14,137.46, 137.02 (d, .1: 3.2 Hz), 129.60 (d, .1: 7.8 Hz), 128.59. . 126.81, 11559 (d, .1 = 21.2 Hz), 109.72, 73.14, 56.99, 5628, 47.81,20.74,19.15,17.92 ‘H NMR (400 MHz. CDCL.) 8 8.40 (s, 1H), 8.32 (d, J: 5.4 Hz, 1H), 7.22 (dd, J = 17.1, 8.2 Hz, 2H), 7.09 (dd,J= 7.2, 2.2 Hz, 2H). 7.06 4 6.96 (m, 3H), 5.69 (dq, J HRMS'ES', : 9.9, 6.2 Hz, 1H), 4.61 4 4.47 (m. 1H), ($171314) 3.96 4 3.92 (m, 1H), 3.90 (s, 3H), 2.38 (s, 3H), 2.32 (s, 3H), 2.30 (s, 3H), 1.22 (d, J calcd for 206 4 6.2 Hz. 3H), 0.99 (d. .14 7.2 Hz. 3H) CdeON01,, 3 13111134 ”C NMR (126 MHz, CDC13) 8 172.16, 573153;] 168.91.162.3015945, 146.64. 141.45, 39.58, 137.47, 136.50. 136.10. , 132.71,130.73,130.63,129.41,129.12, 126,64,126.51, 109.76, 7282, 56.34, 47.83, 20.75, 20.16, 2009, 19.16. 18.00 [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. ”C. 191:) 1H NMR (500 MHz, CDC13) 8 8.30 (d, J = 5.5 Hz, 1H), 8.29 (br s, 1H), 7.26 — 7.18 (m. 4H). 7.01 4 6.88 (m. 5H). 5.70 (dq. J: 9.5, 6.1 Hz, 1H). 4.64 4 4.48 (m. 1H), 4.04 (d, .1: 9.5 Hz, 1H), 3.88 (s, 3H). 1.39 (s. 9H). 1.22 (d. .1: 6.1 Hz.
HRMsiFAB (m z) 3H). 0.99 (d. .1: 7.1 Hz. 3H) ([M+H]+) calcd for ”C NMR (126 MHz, CDC13) 8 176.0, 207 ‘6; (gquFlNZO... 172.3. 162.2. 161.7 (d. .1: 245.8 Hz). ‘ 555.2301; 161.6 (d,J:245.6 Hz), 1594. 1465, found. 1421,1378, 136.9, 136.8, 129.6 (d,J= 555.2311 8.0 Hz). 1295 (d. J: 7.8 Hz). 115.7 (d. .I : 21.3 Hz). 115.4 (d. .1: 21.3 Hz). 109.5. 73.0, 56.3, 56.1, 47.8, 39.1, 27.2, 19.1, ”P NMR (471 MHz. CDC13)8 -115.7, -116.0 1H NMR (400 MHz. CDCL.) 8 8.30 (d. J : 5.4 Hz. 2H). 7.28 4 7.14 (m. 4H). 7.02 — 6.89 (m, 5H), 5.70 (dq, J: 9.5, 6.2 Hz, 1H). 4.63 — 4.48 (m, 1H), 4.04 (d, J: 9.5 HRMS-ESI Hz. 1H). 3.87 (s. 3H). 2.93 (11861. .1: 7.0 (m z) Hz, 1H), 1.34 (d. .1: 7.0 Hz. 6H), 1.22 ([M+H]+) (d, J: 6.2 Hz, 3H), 0.98 (d, J: 7.1 Hz, calcd for 3H) 208 ___ ___ CwHHFZNZOO. 541.2145; 13C NMR (126 MHz, CDC13) 8 174.69, found, 172.21.162.69,162.61, 162.28, 16074, 9 160.66. 159.43. 146.54. 141.81. 137.65. 136.86.136.84,129.64, 129.57, 129.51, 115.76,115.59,115.46,115.30.109.61, 73.03. 56.29. 56.07. 47.79. 33.94. 19.12. 18.80. 18.04 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 8 8.45 — 8.25 (m, 2H), 7.30 — 7.15 (m, 4H), 7.05 — 6.86 (m. 5H). 5.71 (dtd. .1: 9.7. 7.3, 6.8, 55 Hz, 1H), 453 (n, J : 83, 6.6 Hz, 1H), 4.04 (d, .1: 9.6 Hz, 1H), 3.88 (d, J: m’ls'ESI, 1.2 Hz, 3H), 3.80 (td. .1: 6.6. 1.2 Hz. :34) 2H). 3.39 (d, .1: 1.2 Hz, 3H). 2.97 (td, .1 = 67,13 Hz, 2H), 1.22 (dd,.1= 6.3.1.3 calcd for 209 Hz, 3H), 0.98 (dd, J— 7.2, 1.3 Hz, 3H) C2«>H31F2N207. 3511;621:199 ”C NMR (126 MHz, CDC13)8 172.13, 169.42,162.70,162.61,162.25,160.74, “557 20914' 160.66, . 146.69, 141.44. 137.34, 136.87. 136.84, 136.81. . 129.56, 129.50,115.77,115.60,1154111530, 109.78, 73.06, 67.57, 631, 5608, 47.81. 34.62. 19.12.1799 1H NMR (400 MHz, CDCl;) 8 8.33 (dd, J = 19.6, 5.4 Hz, 2H), 7.25 — 7.16 (m, 4H), 7.03 4 6.88 (m, 5H). 5.70 (dq, .1: 95, 6.2 Hz, 1H). 4.65 4 4.52 (m, 1H). 4.04 (61.1: 9.6 Hz, 1H), 3190 (s, 3H), 1.95 (16.1: HREVHIYSZ'FSI, 80,46 Hz, 1H), 1.25 (dd, J: 4.6, 3.1 Hz, 2H). 1.22 (d. .1: 6.2 Hz, 3H)_ 1.05 (I WHF) (dt, J: 8.1, 35 Hz, 2H), 098 (d, J: 72 calcd for 210 ___ ___ Hz 3H) C29H29F2N206, ’ :11?“ ”C NMR (126 MHz. CDCL.) 8 172.45, ,0“ ° 172.20, 162.70, 162.61, 162.26, 160.74, 539.1988 160.66,159.50,146.56, 141.80, 137.45, 136.87, 136.85, , 129.64. 129.57. 129150,115,76,115.59,115,47,115.30, 109.68, 73.03, 56.31, 56.08, 47.75, 19.13, 18.09, 13.00, 9.27 [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 5 8.25 (t, J = 6.2 Hz, 2H), 7.32 — 7.11 (m, 4H), 7.04 4 6.85 (m. 5H). 5.79 4 5.65 (m. 3H). 4.55 (p, J : 7.3 Hz, 1H), 4.04 (d, J : 9.7 Hz, 511321753581 1H), 3.87 (s, 3H), 2.53 (hept, J: 7.0 Hz, 1H). 1.23 (d. .1: 6.2 Hz. 3H). 1.12 (d. .1: (IM+HI+) 7.0 Hz. 6H)_ 0.99 (d. .1: 7.2 Hz. 3H) calcd for 21 1 ___ ___ C3glgigjio7 ”C NMR (126 MHz, CDC13) 5 176.25, ‘ fo11nd * . 162.88. 162.70. 162.60. 160.74. , 160.26, 145.54, 144.21, 142.02, 571 225' 136.94,136.92,136.86, 136.83, 129.60, 129.56. 129.54.129.49. 115.77. . 115.47. 115.30. 109.53. 89.88. 73.01. 56.13,48.05,33.85,19.15,1866,1781 1H NMR (400 MHz, CDClg) 5 8.23 (dd, J : 16.1. 6.6 Hz. 2H). 7.25 4 7.18 (m. 4H). 7.02 4 6.89 (m, 5H), 5.82 4 5.66 (111,3H), 4.54 (p, J: 7.3 Hz, 1H), 4.08 (s, 2H), HRMS—ESI 4.04 (d. .1: 9.7 Hz. 1H). 3.89 (s. 3H). (m z) 3.58 (q. .1 : 7.0 Hz. 2H). 1.25 4 1.20 (m.
([M+H]+) 6H), 0.99 (d, J: 7.2 Hz, 3H) calcd for 212 ___ ___ (gqugFZNZOx. 1~”C NMR (126 MHz. CD(‘,1~.)0 172.20.a 587.2199; 170.05,162.84,162.70, 162.61, 160.75, found, 160.65,160.21,145.73, 143.95, 142.23, 587.2217 136.95. 136.92.136.85. 136.83. 129.60. 129.56. 129.54. 129.50. 115.78. 115.61. 115.47,115.30, , 89.55, 73.04, 67.78, 67.17, 56.23, 56.14, 53.46, 48.04, 19.15.17.81.15.00.1495 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (400 MHz, CDC13) 8 8.45 — 8.22 (m, 2H), 7.30 — 7.15 (m, 4H), 7.04 — 6.89 (m. 5H). 5.71 (dq. .1: 9.5. 6.2 Hz. 1H), 4.63 4 4.45 (m, 1H), 4.04 (d, J: 9.6 HRMS—ESI Hz, 1H), 3.89 (s, 3H), 2.68 (t, J: 7.6 Hz, (777 z) 2H). 1.76 (p. .1: 7.6 Hz. 2H). 1.54 4 1.37 (| M+H|+) (m. 2H). 1.22 (d. .1 : 6.1 Hz. 3H). 1.06 4 calcd for 0.88 (m, 6H) 213 ___ ___ C30H33F2N206a 555.2301; ”C NMR (126 MHz. CDCL.) 8 172.17. found, ,162.70,l62.61, 162.31, 160.74, 160.66,159.47,146.56, 141.61, 137.57, 136.87. 136.85. 136.82. 129.63. 129.57. 129.50. 115,76. 115.60. 115.47. 115.30. 109.69, 73.05, 56.26, 56.08, 47.80, 33.64, 29.70, 26.61, 22.20, 19.12, 18.02, 1376 (Thin 3388, 2970. 2363. 2029, 1738, 1677. 1604, 1508, HRMS—ESI 1H NMR (400 MHz, CDClg) 8 8.28 (d, J 1449. (m z) : 7.8 Hz. 1H). 8.17 (d. .1: 4.9 Hz. 1H). 1414. (|M+Hr) 7.68 (d. .1: 4.9 Hz. 1H). 7.30 4 7.16 (m. 1366, calcd for 4H), 7.05 — 6.90 (m, 3H), 5.81 — 5.69 (m, 1307, BrF3N306, 3H), 4.54 (p, J: 7.3 Hz, 1H), 4.05 (d, J: 1218. 593.0921; 9.8 Hz. 1H). 2.09 (s. 3H). 1.59 (s. 1H). 1203, found, 131 4 1.21 (m, 3H), 1.00 (d, J : 7.2 Hz, 1159, 593 .0925 3H) 1 139. 1 1 13. 1042, 1000, 970, 908. 831. 806, 793, 778, 731, 71 1. 682. 670. 663 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. ”C. 191:) (Thin 3380. 2985, 2362, 1769. 1738. 1H NMR (300 MHz. CDCL) 5 8.38 (d. .1 1674, = 8.0 Hz, 1H). 8.32 (d, J: 5.4 Hz, 1H), 1609, 7.18—6.88 (m, 7H), 5.64 (dq.J= 9.5.6.3 1591. “$752331 Hz. 1H). 4.64 4 4.47 (m. 1H). 4.00 (d. .1: 1572, 93 Hz. 1H), 3,91 (s, 3H). 2.39 (s, 3H).
([M+H]+) 1513, 1.23 (d,J= 6.1 Hz, 3H), 1.09 (d, J: 7.2 “led for 215 1434 Hz 3H) ‘ ‘ 6 C27H25F4N206. 1367* 549 1643 1310, “ foHnd ‘ 11JF NMR (471 MHz, CDC13) 5 -136.31 1277, (ddd,J= 20.1, 11.2, 8.2 Hz), -136.74 549 16;; 1202. ‘ ' “ (ddd..l:2().3. 11.3. 7.8 Hz). 439.144 — 1175, 139.50 (111), —139,70 (dddd,J: 21.4, 1150, 10.6, 7.7, 4.1 Hz) 1 1 13. 1051. 1009, 952. 907, 825, 805. 731. 668, 657 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd MP IR NLASS NMR 190. (‘0 (cnf? (1H. 13C. 191:) (11mm 3375. 2984, 2361, 2132. 1770. 1738, 1676, 1H NMR (300 C13)5 8.38 (d, J 1590. : 8.3 Hz. 1H). 8.31 (c1. .1: 5.4 Hz. 1H). 1H1RdS-ESI 1572, 7.26 (ddd, J: 11,5,7.2,2.1Hz,2H), (n72) 1499, 7.18 — 6.95 (m, 5H), 5.63 (dq, J: 9.3, 6.1 1452. Hz. 1H). 4.65 4 4.49 (m, 1H). 4.00 ((1.7: Cdcd?n 216 1437. 9.4 Hz. 1H). 3.91 (s. 3H). 2.39 (s. 3H).
C27H25C12F2N 206: 1367, 1.24 (d, J: 6.2 Hz, 3H), 1.09 (d, J: 7.2 581.1052; 131L Hz, 3H) found. 1251. 581.1061 1199, ”P NMR (471 MHz, CDC13)8 -116.85 4 1175, -117.26 (111), -117.29 — -117.50 (In) 1098. 1061. 1010,952, 907,828, 805,782. 764,733, 687,668, 657,651 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd MP IR N1\1IR N0. (‘0 (cm'l) (1H, 13C. 191:) (11mm 33 3. 2983. 1771, 1736. 1676. 159L 1H NMR (300 MHz. CDC13) 8 8.40 (d, J 1572. = 8.2 Hz, 1H). 8.32 (d. J: 5.4 Hz, 1H), 1503. 1H{RJS-ESI 7.14 4 6.96 (m. 5H). 6.96 4 6.81 (m. 2H). 1451. (/77 Z) 5.68 (dq, J: 9.9, 6.1 Hz. 1H). 4.53 (dt. J 1437, ([M+H1+) = 8.2, 7.1 Hz, 1H). 3.94 (d,J= 10.0 Hz, 1366. cmcd?n 1H). 3.90 (s. 3H). 2.38 (s. 3H). 2.22 (dd. 1311. (729H21F2N206. .1: 6.7.1.9 Hz. 6H). 1.21 (d. .1: 6.1 Hz. 1271 541.2145; 3H), 0.98 (d, J: 7.1 Hz, 3H) 1237. found. 1201. 541.2156 ”P NMR (471 MHz. CD(‘,1~,)5 1176, —119.90 4 —120.14(m). 0 4 1119, -12065(nD 1099. 1051. 1009.949. 907.825. 733.668.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. ”C. 191:) (Thin 3376. 2988. 2363, 1742. 1675. 1H NMR (300 MHz. CDCL.) 8 8.27 (d. .1 1609, = 5.4 Hz. 1H). 8.21 (d. J: 7.8 Hz. 1H), 1580. 7.18 — 6.85 (111.7H).5.72(s,2H). 5.65 1515. SI (dq. .1: 10.5. 6.2 Hz. 1H). 4.58 (p. .1: 1454. 7.3 Hz. 1H). 4.01 (d. J: 9.4 Hz, 1H). 1435, calcd for 3.913s. 3H). 2.07 (s. 3H). 1.25 (d. J: 5.9 218 1.368. Hz. 5H). 1.09 (d. .14 7.2 Hz. 5H) szHl—HNzOz. 1310* 579 1749 1284, ' foHnd ‘ 11)F NMR (471 MHz. CDC13) 5 1236. —136.29 (ddd.J= 20.1. 11.2, 8.0 Hz). — 1203. ‘S79 1762' 136.73 (ddd. .1: 20.1. 11.3. 8.0 Hz). — 1181, 139.16 4 —139.43 (m). -139.64 4 1149, -139.84 (In) 1 120. 1043. 1004. 970. 910. 873. 829. 754.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd MP IR ‘NBIR NLASS 190. (‘0 (cnf? (1H, 13C. 191:) (11mm 3393. 2986, 2364, 1742. ‘H NMR (300 MHz. ~,) 5 8.27 (dd. .1 1676. :54, 1.1 Hz, 1H), 8.21 (d,J: 7.8 Hz, 1580, 1H), 7.35 — 7.19 (m, 2H), 7.20 — 7.01 (m, 1499, PHRRJS-ESI 4H). 6.96 (dd. .1: 5.5. 1.1 Hz. 1H). 5.72 1454. (/77 22) (d. .1: 1.1 Hz. 2H). 5.64 (dddd. .1: 11.6. 1437, ([M+H]+) 9.1, 5.3, 3.3 Hz, 1H), 4.65 — 4.51 (m, 1408, calcd for 1H), 4.01 (d, .1: 9.5 Hz, 1H), 3.92 (d, J: 219 1367. (123H27C13F3N307. 1.1 Hz. 3H). 2.07 (c1. .1: 1.1 Hz. 3H). 1310. 611.1158; 1.304121 (111,311), 1.09(dd,J: 71.11 1250, fbund, Hz, 3H) 1202, 611.1169 1180.
”P NMR (471 MHz. C150.) 5 1148, -116.92 — -117.10 (111), -117.36 — 1101, -11753(nD 1061. 1044. 911,829, 732.72(l ation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) (Thin 3375. 2986, 1738, 1675. 1 H NMR (300 MHz. .). . - C) 8.27 (d. .1 “01‘ :54 Hz, 1H), 8.21 (d,J:7.8 Hz, 1H), 1452’ HRMS—ESI 7.05 (td, J: 9.7, 8.2, 4.2 Hz, 4H), 6.98 — 1437’ (m z) 6.82 (m. 3H). 5.78 7 5.54 (m. 3H). 4,63 2 1366* (|M+H| ) 4.48 (m. 1H). 3.95 (d. .1: 10.1 Hz. 1H). calcd for 3.91 (s, 3H), 2.22 (dd, J: 6.4, 2.0 Hz, ___ 1310’ 127; C30H33F3N307, 6H), 2.06 (s, 3H), 1.23 (d, .1: 6.1 Hz, 1237‘ 5712250; 3H). 0.99 (d. .1: 7.2 Hz. 3H) 1262‘ found, _ 19 A “80’ 5712265 F NMR (471 MHz, CDC13)o —120.03 (dt. .1: 9.7. 5.9 Hz). —120.57 (dd. 1 151’ .]:8.8.5.4 Hz) 1101, 1043. 1003. 970. 909, 828, 785, 730 ‘H NMR (300 MHz. CD(‘,1~,) 8 8.27 (d. .1 : 5.4 Hz, 1H), 8.20 (d, .1: 7.8 Hz, 1H), 7.42 — 7.29 (m, 4H), 7.12 (dd, J: 8.3, 2.2 Hz. 1H). 7.08 (dd. .1: 8,3. 2.2 Hz. 1H).
HRMS-ESI 6.95 (d. .1: 5.4 Hz. 1H). 5.72 (s. 2H). (mz) 5.70—5.58 (m, 1H), 4.58 (p,J= 7.2 Hz, ([M+H]+) 1H), 4.00 (d, .1: 9.5 Hz, 1H), 3.91 (s, calcd for 3H). 2.07 (s. 3H). 1.26 (d. .1: 6.2 Hz.
C28H37C11N207, 3H), 1.10 (d, .1: 7.2 Hz, 3H) 643.0567; found. 13C NMR (126 MHz. CDC1~.) 8 172.13. 643.0578 170.29. 162.96. 160.28. 145.71. 144.01. 142.25, 140.34, 133.06, 132.72, 131.62, 131.29,130.94,130.67,130.34.130.11, 127.32. 10964. 89.50. 72.10. 56.20. 5571, 48.07, 20.88, 19.07, 17.85 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) 1H NMR (300 MHz, CDC13)5 8.27 (d, J = 5.4 Hz, 1H), 8.20 (d, J: 7.8 Hz, 1H), 7.32 (td. .1: 8.3. 7.6 Hz,2H),7.11 4 6.93 (111,411), 5.72 (d,J: 0.5 Hz, 3H), 5.71 4 .60 (m, 1H), 4.67 — 4.51 (m, 1H), 4.03 ((1.1: 9.3 Hz, 1H). 3.91 (s, 3H). 2.07 (s, HREijI, 3H). 1.26 (d, .1: 6.2 Hz, 3H). 1,09 (d. .1: 7.2 Hz, 3H) ([M+H]+) C 5111501; 0 ”C NMR (126 MHz, CD(‘,1~,)5 172.10, ’2“ 61171 13538? 7‘ 170,29, 162.95, 160.29, 158.15 (d, J: ' c1 ‘ 250.2 Hz), 158.01 (d, J: 249.8 Hz), (131111173;f 145.70. 144.03, 142.24, 141.03 (d, .1: ’ ' ‘ 6.5 Hz), 131.08. 130.80, 124.51 (d. .1: 3.5 Hz), 124.40 (d, J: 3.6 Hz), 120.03 (d,J= 17.6 Hz), 119.73 (d,J= 17.7 Hz), 116.55 (d, .1: 21.8 Hz), 109.64. 89.51, 72.15, 56.20, 55.99, 48.05, 20.87, 19.03, 17.84 1H NMR (300 MHz. CDCL.) 8 8.80 (d. J : 6.6 Hz. 1H). 8.49 (d. .1: 6.8 Hz. 1H). 7,58 (d, J: 66 Hz, 1H), 7.40 — 7.27 (m, IMO‘EYSZFSI, _ 4H), 7.14 — 7.01 (m, 2H), 5.67 — 5.52 (m, 1H). 4.61 4 4.46 (m. 1H). 4.18 (s. 3H). (1191mm 410 (d, J: 99 Hz, 1H), 2,44 (s, 3H), calcd for 223 1.27 (dd, J: 6.3, 3.1 Hz, 6H) C27H25C11N306, 6%;23'; ”C NMR (126 MHz. CDCL.) 8 174.00, 3‘ ° ,170.13,140.79, 140.20, 133.07, 613.0468 13234, 131.62, 130.97, 130.85, 13055, 130.04, 127.30, , 108.57. 72.40, 58102, 55.48, 34.67, 18.65, 16.34 [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H. ”C. 191:) 1H NMR (300 MHz. CDC13) 8 8.88 (d, J = 6.7 Hz. 1H). 8.49 (d. J: 6.7 Hz. 1H). 7.67 (d. .1: 6.7 Hz. 1H). 7.38 4 7.28 (m. 2H). 7.09 4 6.95 (m. 4H). 5.68 4 5.49 (m. 1H), 4.59 4 4.48 (m. 1H). 4.21 (s. 3H), 4.12(d..1: 9.8 Hz. 1H). 2.44 (s. 3H). 1.31 4 1,24 (m. 6H) HRMS-ESI (“8171214) ”C NMR (126 MHz. CDC13) 8 174.30. 171.60. 170.11. 157.88 (61.1: 307.7 Hz). calcd for 224 14143 (d. J: 6.1 Hz). 14087 (d. J: 6.2 C H @171: N 027 5:51 {0:22 6’ Hz),131.11. 130.71. 124.43, 123.96 (d,J ' fo11n c1 ‘ : 3.6 Hz). 120.02 (d. .1: 17.7 Hz). $811039 119.27 (d. .1: 17.3 Hz). 116.85 (d. .1: “ ' “ 21.3Hz).116.32(d.J=21.5Hz). 108.58. 72.61. 58.04. 55.77. 50.35. 31.59. 18.66. 16.35 19F NMR (471 MHz. CDC13) 8 -113.83 4 41 13.93 (m). 41 14.77 (t. .1: 8.7 1H NMR (300 MHz. CDC13) 8 8.27 (d, J = 5.4 Hz. 1H). 8.13 (d. J: 7.8 Hz. 1H). 7.25 4 7.14 (m. 4H). 6.93 (dddd. .1: 18.3. 8.7. 6.6. 2.1 Hz. 5H). 5.75 4 5.61 (m.
HRMS—ESI 3H), 4.64 4 4.42 (m. 1H). 4.05 (d. J: 8.9 (m z) Hz. 1H). 3.91 (s. 3H). 2.05 (s. 3H). 1.31 (|M+Hr) (d. .1: 7.1 Hz. 3H). 1.21 (d. .1: 6.2 Hz. calcd for 3H) 22; ___ ___ F2N2074 543.1937; ”C NMR (126 MHz. CD(‘,1~.) 8 171.93. found, 170.30.162.76.162.66, 160.62. 160.36. 543.1949 145.64.144.15,142.26. 136.92. 136.54, 129.80. 129.74. 129.69. . 115.71. 115.54. 115.42. 115.25. 109.59. 89.62. 73.10, 56.21, 55.59. 48.03, 20.86. 18.95, 18.06 ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) (Thin 3375, 33%L 1H NMR (400 MHz, CDC13) 5 6.95 — 6.77 (m, 4H), 5.57 (dq, J: 9.0, 6.2 Hz, 1:; 551? _ 1H). 4.91 (d. .1: 7.8 Hz, 1H). 4.27 2 4.13 1448‘ [M+Na]+ (m, 1H), 3.93 (d, .1 : 9.0 Hz, 1H), 1.42 (s, 1,6; 9H), 1.24 (d, .1: 6.2 Hz, 3H), 1.00 (d, J: 1 d f 226 i “a C or . 7.2 Hz, 3H) 1346,1, (,2;H2;F(,NNaO4. 3i: 3 11166113); ”F NMR (376 MHz, CDC13) 5 1165’ -132.38 (d, J: 20.6 Hz), —132.83 (d,J= 614 Mix ”1‘7‘ ‘ ' 20.6 Hz). —160.90 (t. .1: 20.5 Hz). 1094* —161.25 (t, J: 20.6 Hz) 1043, 863, 803, 786, 729, 679 (Thin 2939, 2031, 1H NMR (400 MHz, methanol-d4) o 7.36, 2 7.17 (m, 4H). 5.83 : 10.0, 6,] 1:32 HR37I7SZ)ESI? _ Hz, 1H). 4.26 (d, .1: 10.1 Hz, 1H)_ 4.00 1447’ ([M+H]+) (q, J: 7.2 Hz, 1H), 3.31 (p, J: 1.7 Hz, 3H), 1.28 (d, .1: 6.2 Hz, 3H), 1.08 (d, J: 134; Wed for 227 7‘2 HZ‘ DH) 1234, CMHMFGNOZ, 1118 ”£33130; 19F NMR (376 MHz, methanol-d4) 5 1041’ —137.08 (d, .1: 20.0 Hz), —137.39 (5.1: 8‘72 *392 1083‘ * 19.9 Hz). —166.29 (t. .1: 19.9 Hz). 826 .802 ° -166.61 (t, J: 19.9 Hz) 752, 729, 707, 680, 666, 659 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) (Thin 33 3, 2942, 1738, 12:: ‘H NMR (400 MHz. CD(‘,1~,) 8 1 1.93 (s, _ 1H), 8.29 (d, J: 7.9 Hz, 1H), 7.98 (d, J: 13;; “(17717531351_ 5.2 Hz. 1H), 6.94 — 6.77 (m, 5H), 5.58 {481’ (|M+H|+) (dq,.I:9.0_ 6.2 Hz. 1H).4.65 44.49 (m, 1446,,, , 1H). 3.94 (d, .1: 5.5 Hz. 4H). 1.25 (dd. .1 calcd for 228 ___ = 9 4 6 7 Hz 6H) 1344, C25H31F6N205, ' = ' 3 363 59; ”P NMR (376 MHz. CDCL) 5 1211‘ 543L112 52 —132.34 (d, J : 207 Hz), —132,74 (d, J : 3' 3 .5 Hz), -160.82 (t, J: 20.5 Hz), 1148’ 1117, —161.08 (1.1: 20.5 Hz) 1094, 1040, 984, 954, 909. 849, 801. 727, 678 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C, 191:) (Thin 3384, 2985, 1770, 1741, 1676, 1H NMR (400 MHz, CDCL) 5 8.37 (d, .1 1622, = 7.6 Hz, 1H), 8.32 (d, J: 5.4 Hz, 1H), 1592, , 7.01(d,J= 5.5 Hz, 1H), 6.88 (dd, J: 1572, HRS/7128;“ 8.1, 6.3 Hz, 2H), 6.82 (dd, .1: 8,1, 6.2 1527, Hz, 2H), 5.56 (dq, J: 8,7, 6.2 Hz, 1H), ([M+H]+) 1447, 4.65 — 4.50 (m, 1H), 3.94 (d,J= 8.8 Hz, calcd for 229 1368, 1H), 3.91 (s, 3H), 2.38 (s, 3H), 1.24 (d, J (,7 HF N70 1345, [58571455 "‘ : 6.2 Hz, 3H), 1.18 (d, .1: 7.2 Hz, 3H) 1312, ' " 1237, 53111364 19F NMR (376 MHz, CDC13) 5 1199, 5 5' —132.51 (d. .1: 20.5 Hz), —132.94 (d, .1: 1176, 20.4 Hz), —161.06 (t, J: 20.5 Hz), 1117, -l61.30(t,J=20.6Hz) 1095, 1042, 1010, 954, 909, 846, 828, 803, 729, 680 ation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR MASS, N0. (0C) (cm'l) (H, ”C. 191:) (Thin 3384. 2987, 1743, 1675. 1 H NMR (400 MHz. CD(,1~.). - C) 8.27 (d. .1 ”79‘ :34 Hz, 1H), 8.20 (d,J: 7.7 Hz, 1H), 17,26 6.96 (d,J= 3.4 Hz, 1H), 6.90 (dd, J: 1306’ HRMS—ESI 8.2. 6.3 Hz. 2H). 6.84 (dd. .1: 8.0. 6.2 1447* (m z) Hz. 2H). 3.72 (d. .1: 1.0 Hz. 2H). 3.38 ([M+H]+) (dq,J= 8.9, 6.2 Hz, 1H), 4.59 (p, J: 7.3 1366’ calcd for Hz, 1H), 3.96 (d, J: 8.8 Hz, 1H), 3.92 (s, 2,0‘ 1344’ 131 szH?F?NZOz 3H). 2.07 (s. 3H). 1.26 (d. .1: 6.2 Hz. * 1‘ * 615.1560; 3H), 1,17(d,./:7,3 Hz, 3H) 1237, 1201. fciunfl’ 19 ”80 613.1370 FNMR (376 MHz. CDC];)0- “49‘ 43249 (d. .1: 20.7 Hz). 43292 (d. .1: 1117: 20.6 Hz), -161.02 (t,J=20.6 Hz), -161_33 (t,J=20.6Hz) 1101. 1040. 1003, 971, 911, 830, 803. 728.
ESIMS m z 320 (11141110 1H NMR (400 MHz. CDC1~,) 5 7.21 (ddd. .1: 11.8. 8.4. 3.2 Hz. 4H). 6.98 (td. .1: 8.6, 5.6 Hz, 4H), 5.67 (dq, J: 9.2, 6.2 Hz, 1H), 4.80 (d,J= 7.8 Hz, 1H), 4.06 ESIMS (dd. .1: 21.8. 8.4 Hz. 2H). 1.43 (s. 9H). mz420 1.18 (dd,J: 12.5, 6.7 Hz, 6H) ([M+H]+) 13C NMR (126 MHz. CDC1~.) 5 172.42. 162.70. 162.62. 160.74. 160.67. 136.89. 136.87,129.74,129.67, , 113.76, 115.59, 113.47, 115.30, 79.79, 72.77, 55.76.419.40. 30.93.2830. 19.00. 18.30 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd.
MASS N1VJR No, (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.25 4 7.17 (m, 1H), 7.14 (dd, J: 8.4, 5.8 Hz, 1H), 6.91 — 6.76 (m, 4H), 5.60 (dq, J: 9.8, 6.2 Hz, 1H), (Thin ?lm) HRMS-ESI (m Z) 4.94 (d, .1: 8.0 Hz, 1H), 4.42 3367, 2979, ([M+Na]_) calcd for (d, J: 9.8 Hz, 1H), 4.12 (qd, 234 1708, 1495, F3NNaO4, J: 7.2, 2.5 Hz, 1H), 2.37 (s, l 162, 1049, 470.21 13, found, 3H), 2.32 (s, 3H), 1.42 (s, 731 470.21 10 9H), 1.29 (d, .1: 61 Hz, 3H), 0.88 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) —116.52, -11701. 1H NMR (400 MHz, CDC13) 7.33 4 7.17 (m, 8H), 5.77 : 10.3, 6.1 Hz, 1H), 4.97 (d, J: 7.9 Hz, 1H), 4.10 (dq,J= 14.6, 7.2 Hz, 1H), 3.95 (d, .1: 103 Hz, 1H), (Thin ?lm) HRMS-ESI (m/z) 1.41 (s, 9H), 1.26 (s, 9H), 3440, 2963, ([M+Na]_) calcd for 1.25 — 1.20 (m, 12H), 0.64 235 1708, 1365, C31H45NN304, (d, .1: 7.2 Hz, 3H). 1164, 1051, 518.3241; found, 908, 731 518.3245 13C NMR (101 MHz, CDC13) 5 172.88, 154.92, 149.54, 149.34, 138.80, 138.25, 127.65, 127.61, 125.59, 125.29, 79.54, 73.50, 57.27, 49.13, 34.34, 34.29, 31.30,28.31,19.36, 17.73.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No. (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 6 7.244 7.17 (m, 4H), 7.164 7.05 (m, 4H), 5.76 (dq, J : .2, 6.1 Hz, 1H), 4.97 (d, J = 7.9 Hz, 1H), 4.09 (dq, .7: 17.8, 7.3 Hz, 1H), 3.95 (d, .1 = 10.3 Hz, 1H), 2.82 (dhept, J: 9.4, 6.9 Hz, 2H), 1.41 (s, HRMS-ESI (m 2) 9H), 1.22 (d, .1: 6.2 Hz, (Thin ?lm) ]‘) calcd for 3H), 1.17 (dd,J= 11.6, 6.9 3373,2960, 236 C29H41NNaO4, Hz, 12H), 0.67 (d, J: 7.2 1711,1163, 490.2928; found, Hz, 3H). 1050, 731 490.2931 13C NMR (101 MHz, CDC13)6172.87, 154.93, 147.27, 147.10, 139.20, 138.70, 127.91, 127.88, 126.75, 126.44, 79.54, 73.45, 57.42, 49.16, 33.64, 33.60, 28.31, 2400,2397, 23.91, 19.35, 17.79. 1HNMR (400 MHz, CDC13) 6 7.16 — 6.89 (m, 6H), 5.73 (dq,.1: 102,61 Hz, 1H), (Thin ?lm) HRMS-ESI (m 2) .04 — 4.90 (m, 1H), 4.19 — 3364, 2976, ([M+Na]_) calcd for 4.02 (m, 1H), 3.88 (d, J: 237 1712, 1501, C27H3-NNaO4, .3 Hz, 1H), 2.17 : 1450, 1162, 462.2615, found, .4, 9.0 Hz, 12H), 1141(s, 1052, 731 462.2623 9H), 1.22 (d, J: 61 Hz, 3H), 0.79 (d, .1: 7.1 Hz, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. n .
:\L \\\\\ ‘\‘\1 MP MASS NMR No. \'\'\x ‘ ~‘ (‘0 (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.23 (ddd, J: 16.6, 8.5, 5 ,, .3 Hz, 4H), 6.97 (td, J: 8,7, 2.2 Hz, 4H), 5.69 (dq, J = 9.1, 6.2 Hz, 1H), 4,93 (d, J 7.3 Hz, 1H), 4.08 (dd, .1: 21.8, 8.3 Hz, 2H), 1.43 (s, 9H), 1.18 (dd,J= 13.2, 6.7 Hz, 6H).
ESIMS m z 442 ([M+H]+) 4R(1011V1Hz, CDC13) 5 172.40, 162.91, 162.84, 160.46, 160.40, 154.90, 136.97, 136.94, 136.66, 129.81, 129.73, 129.69, , 129.53, 115.76,115.71,115.55, ,115.43,115.22, 79.65, 77.45, 77.13, 76.81, 72.71, 55.71, 49.44, 28.25 7 1892,1810.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd.
MASS NMR No, (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.23 (ddd, J: 15.9, 8.7, 5.4 Hz, 4H), 6.97 (dtd, J : 8,7, 6.4, 2.1 Hz, 4H), 5.71 (dq, J = 9.8, 6.1 Hz. 1H), 4.98 (d, J : 7.8 Hz, 1H), 4.14 (dq,.]: 14.9, 7.6 Hz, 1H), 4.03 (d, J = 9.8 Hz, 1H), 1.42 (s, 9H), ESIMS m z 420 1.22 (d, J: 6.1 Hz, 3H), 0.84 ([M+H]+) (d, J: 7.2 Hz, 3H).
”C NMR (101 MHz, CDC13) 5 172.75, 162.96, 162.88, 160.51, 160.43, 154.94, 137.01, 136.97, , 136.82, 129.58, 129.53, 129.51, 129.45, 115.80,115.59,115.49, 115.28, 79.71, 72.86, 56.20, 49.18, 28.28, 19.17, 18.02. lH NMR (400 MHz, CDCH) 8 7.34 (dd, J: 8.6, 67 Hz, 1H), 7.12 (dd,J= 87,67 Hz, 1H), 6.64 4 6.44 (m, 4H), 5.85 (dq,J: 9.5, 6.1 (Thin ?lm) HRMS-ESI (m/Z) Hz, 1H), 4.96 (d, J = 7.8 Hz, 3355, 2978, ([M+Na]‘) calcd for 1H), 4.81 (d, J: 9.8 Hz, 240 1711, 1599, C25H31F2NN306, 1H), 4.23 4 4.02 (m, 1H), 1500, 1162, 502.2012, found, 3.82 (s, 3H), 3.74 (s, 3H), 954 502.2021 1.42 (s, 9H), 1.20 (d, J: 6.2 Hz, 3H), 0.88 (d, J: 7.2 Hz, "’1? NMR (376 MHz, CDClg) -113.46, -113.83.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS N1VJR No. (‘0 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.30 - 7.13 (m, 10H), 5.83 (q, J: 6.4 Hz, 1H), 5.00 (d, J: 5.4 Hz, 1H), 4.26 —4.12 (m, 1H), 1.73 (s, 3H), 1.41 (s, 9H), 1.15 (d, .1: 6.3 Hz, ESIMS 777 Z 398 3H), 0.98 (d, J: 7.2 Hz, ([M+H]+) 3H). l3(:1\11\4R(1011\4Hz, CDC13)6172.77, 154.93, , 145.15, 128.16, 128.10, 127.92, 127.40, 126.28, , 79.69, 75.78, 50.38, 49.39, 28.3], 23.89, 1837,1598. 1H NMR (400 MHz, CDCl;) 7.65 4 7.56 (m, 4H), 7.43 4 (Thin ?lm) 7.33 (m, 4H), 5.85 — 5.73 (m, ESIMS mz 434 3375, 2980, 1H), 4.87 (d, J: 7.9 Hz, 242 ([M+H]+) 2934, 2229, 1H), 4. 19 (dd, .1: 9.3, 2.7 1739, 1708, Hz, 1H), 4.17 —4.01(m, 1605, 1504 1H), 1.42 (s, 9H), 1.25 (d, J : 6.2 Hz, 3H), 0.85 (d, .7: 7.2 Hz, 3H), 1H NMR (400 MHz, CDC13) 7.56 (w: 8.1 Hz, 4H), 7.44 — 7.36 (m, 4H), 5.89 — (Thin ?lm) ESIMS m 'z 520 N} 5.76 (m, 1H), 4.89 (d, .1: 7.8 3357, 2982, ([M+H]+) Hz, 1H), 4.19 (d,./ : 9.8 Hz, 1709, 1617, 1H), 4.12 (t,J= 7.5 Hz, 1H), 1.41 (s, 9H), 1.26 (d, J: 6.2 Hz, 3H), 0.79 (d, .1 : 7.2 Hz, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS N1VJR No. (cm ) (1H7 13c:1 19F) 1:1 mixture of diastereomers. 1H NMR (500 MHz, CDCl;) 7.32 4 7.23 (m, 8H), 7.22 4 7.13 (m, 2H), 5.84 — 5.72 (m, 1H), 4.93 (d, J: 7.9 Hz, 1H), 4.77 (d, .1: 6.2 Hz, 1H), 4.15 — 4.00 (m, 2H), 1.42 (s, 9H), 1.24 (d, J = 6.3 Hz, 3H), 1.22 (d, .1 : 6.0 Hz, (Thin ?lm) HRMS-ESI(/1Iz) 3H),1.11(d,J= 7.2 Hz, 3361, 2978, +) 3H), 0.76 (d, J = 7.2 Hz, 1709, 1494, calcd for 3H). 244 1450, 1365, C23H30NO4, 1162, 1050, 384.2169, found, (126 MHz, 1029, 731, 384.2169 CDC13)6172.83, 172.30, 154.93, 141.50, 141.26, 128.77, 128.73, 128.49, 128.46, 128.23, , 128.08, 128.05, 126.90, 126.87, 126.66, 79.64, 73.11, 73.03, 57.97, 57.54, 49.46, 49.17, 34.67, 28.32, .28, 20.70, 19.30, 19.10, 18.31, 18.00. 1H NMR (400 MHz, CDC13) 7.31 (d, J: 8.2 Hz, 1H), 7.09 (d, .1: 8.1 Hz, 1H), 6.87 (dd, J: 82,20 Hz, 1H), 6.83 (dd,J= 8.1, 2.0 Hz, (Thin ?lm) FIRMS-E81011 ”2) 1H), 6.79 (dd, .1: 14.8, 2.0 3374, 2977, ([M+Na]‘) calcd for Hz, 2H), 5.84 (dq, J : 12.4, 245 1711,1592, C25H31C12NN306, 6.2 Hz, 1H), 4.95 (d, J: 7.3 247, 534.1421, found, Hz,1H),4.81(d,J= 9.7 Hz, 1163,1029 534.1427 1H), 4.26 4 4.01 (m, 1H), 3.82 (s, 3H), 3.74 (s, 3H), 1.42 (s, 9H), 1.20 (d, J: 6.1 Hz, 3H), 0.89 (d, .1 : 7.2 Hz, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.30 (dd, J: 8.5, 6.8 Hz, 1H), 7.14 (dd, J: 8.5, 6.8 Hz, 1H), 6.61 — 6.43 (m, . 4H), 5,87 (dq, J: 126, 6.3 $22)“ $912}; HRMS—ESI (m z) Hz, 1 H), 4.97 (d, .1 : 6.9 Hz, 1710’ 1598’ ([M+Na]‘) calcd for 1H), 4.80 (d, J: 10.1 Hz, 246 C27H35F2NNa06, 1H), 4.21 — 4.07 (m, 1H), 1 500’ 1274’ 116010407 530.2325, found, 4.064378 (m, 4H), 1.564 9901821 7 36 ,15H),1.21(d,J= 1 6.1 Hz, 3H), 0.90 (d, J: 7.2 Hz, 3H). 191: NMR (376 MHz, CDC13) 8 -11372, -114.20. 1H NMR (400 MHz, CDC13) 7.27 (d, .1: 8.1 Hz, 1H), 7.10 (d,./: 8.2 Hz, 1H), ()84 (dd, J: 5.6, 2.6 Hz, 1H), 6'81 (dd’ J‘ 83120 HZ” (Thin ?lm) HRMS—ESI (m z) 1H)’ 6'75 (dd’ ‘1 7 3358, 2979, ([M+Na]‘) calcd for 1449’ 2‘0 Hz, 2H), 5.86 (dq, J— 12.2, 247 1711, 1592, C27H35C12NNa06, 6.1 Hz, 1H), 4.98 (d, J— 6.9_ 1491,1247, 562.1734, found,, , HZ 1H) 480(d 1:100 1162,1042 562.1737 ’ 1 ‘ 1‘ ‘ Hz, 1H), 4.23 — 4.07 (m, 1H), 4.07 — 3.75 (m, 4H), 1.52 41.34(m,15H), 1.21 (d, J: 6.2 Hz, 3H), 0.91 (d, J = 7.2 Hz, 3H). ation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS N1VJR No, (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.25 (d, .1: 7.7 Hz, 1H), 7.12 (d, J: 7.8 Hz, 1H), 6.69 — 6.52 (m, 4H), 5.89 (dq, J: (Thin ?lm) HRMS—ESI(I17Z) 12.3, 6.1 Hz. 1H), 5.03 (d, J 3360, 2977, ([M+Na]‘) calcd for : 6.7 Hz, 1H), 4.88 (d, .1: 248 1712, 1504, C29H41NN306, 10.2 Hz, 1H), 4.10 (q,J= 1259, 1161, 522.2826; found, 12.8, 9.8 Hz, 1H), 4.05 — 1044 52228 19 3.78 (m, 4H), 2.26 (s, 3H), 2.24 (s, 3H), 1.53 —1.33(m, 15H), 1.22 (d, J: 6.2 Hz, 3H), 0.86 (d, .1: 7.1 Hz, 1H NMR (400 MHz, CDCH) 8,02 4 7.89 (m, 4H), 7.40 4 7.29 (m, 4H), 5.89 — 5.75 (m, 1H), 4.91 (d, .1: 80 Hz, 1H), 4.35 (q,.]: 7.1 Hz, 2H), 4.34 (q, J: 7.1 Hz, 2H), 4.18 (d, J: 99 Hz, 1H), 4.16 4 4.03 (m, 1H), 1.41 (s, 9H), 1.37 (t,J= 7.1 ESIMS m z 528 Hz, 6H), 1.24 (d, J: 6.2 Hz, 249 ([M+H]+) 3H), 0.81 (d, .1: 7.2 Hz, 13C NMR (101 MHz, CDC13) 5 172.71, 172.69, 166.18, 166.10, 145.69, 145.36, 130.18, 129.91, 129.56, 129.31, 128.25, 128.12, 72.36, 60.98, 60.95, 57.67, 2829, 19.18, 18.09, 14.29, 14.28.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. :32; MP IR NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 6.65 4 6.51 (m, 4H), 6.46 (tt, J: 10.3, 2.3 Hz, 2H), .67 (dq,J= 10.0, 6.1 Hz, 1H)” 4'98 (d’ J: 7‘9 HZ° (Thin ?lm) FIRMS—13810112) - 14(dd,.1410.5,4,8 \ 3378, 2979,M ([M+Na] )calcd for ’ 1H) 3 92 ((1 J29 9H2 250 \ 1707, 1592, C25H31F2NNa06, ,1 ‘ ,1 ‘ 1 ~:\ 1453, 1134, 502.2012; found, ,lH)‘ 3'76 (3’ 3H) 3‘75 (3‘ 3H), 1.42(s, 9H), 1.24 (d, .1 1050 731 502 2022 1 ' = 6.2 Hz, 3H), 0.88 (d, J = 7.2 Hz, 3H).
”P NMR (3 76 MHz, CDC13) -110.64, —111.21. 1H NMR (400 MHz, CDC13) 6 6.45 (dd, J: 4.5, 2.2 Hz, 4H), 6.28 (dt, .1: 13.7, 2.2 Hz, 2H), 5.73 (dq, .1: 10.3, 6.1 Hz, 1H), 5.00 (d, J: 7.9 Hz, 1H), 4,12(tt,J=7.1, 3.3 Hz, 1H), 3.87 (d, .1: 10.4 (Thin ?lm) HRMS-ESI (mz) Hz, 1H), 3.75 (s, 6H), 3.73 \ 3375, 2978, ([M+Na]‘) calcd for (s, 6H), 1.42 (s, 9H), 1.24 (d, 251 1708, 1593, C27H37NNan, .l: 6.1 Hz, 3H), 0.84 (d, .1: 1456, 1149, 526.2411; found, 72 Hz, 3H). 1059, 729 526.2409 13C NMR (101 MHz, CDCl;,) 6 172.84, , 160.78, 154.94, 143.51, 143.22, 106.45, 106.20, 98.58, 98.44, 79.63, 72.69, 58.27, 55.28, 55.26, 49.25, 28.31, 19.27, 18.07. ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No. (0C) (cm'l) (1H,1”C,19F) 1H NMR (400 MHz, CDC13) 6.69 (s, 2H), 6.66 4 6.62 (m, 2H), 6.54 (s, 1H), ()50 (s, 1H), 5.72 (dq, J: 10.4, 6.1 Hz, 1H), 5.00 (d, .1: 7.9 Hz, 1H), 4.22 4 4.00 (m, 1H), 3.86 (d, J: 10.4 Hz, 1H), 3.74 (s, 3H), 3.73 (s, (Thin ?lm) 3H), 2.28 (s, 3H), 2.25 (s, HRMS-ESI(/1Iz) 3370, 2978, 9'5;1(9/ 3H), 1.41 (s, 9H), 1.22 (d, J ([M+Na]_) calcd for 1708, 1594, = 6.2 Hz, 3H), 0.80 (d, J: 1454, 1292, C27H3115Na06’ 7.1 Hz, 3H). in: 494.2513; found, 1155,1051,4 494 2510 1 729 ' 1"CN1\/IR(1011\4HZ, CDC13)6172.85, 159.78, 159.65, , 142.79, 142.49, 139.72, , 121.29, 112.72, 112.69, 111.34, 110.84, 79.59, 72.99, 57.93, 55.12, 55.11, 49.24, 2832,2165, 2158,1931, 18.02.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H. 13C. 191:) 1H NMR (400 MHz. CDC13) 7.00 (ddd. .1: 13.3. 7.6. 0.9 Hz. 2H). 6.85 i 6.68 (m. 4H). 5.78 (dq. J: 10.3. 6.1 Hz, 1H). 5.11 —4.82 (m. 1H).4.12(qd..1:7.1.2.3 Hz. 1H). 3.94 (d. J: 10.2 Hz. 1H). 3.79 (s. 3H). 3.78 ' 2 (5‘ (Thin ?lm) SI (m z) (3’ "1112”“ 3H)” 2‘ . 3H).1.41(s.9H).124(d.J 3377. 2978. ([M+Na] for :61Hz 3H) 080(d J: 253 1711.1508. C27H3+NNa06. ' 712mm) ’ 1252.1163. 4942513150115. ‘ ’ ‘ 1041. 732 494.2493 13CN1\4R(1011V1Hz.
CDC13)6172.87. 157.86. 157.65. 154.93. 140.45. 140.25. . 130.47. 125.22. 124.79. 119.74. 119.69. 109.82. 109.77. 79.64. 73.09. 57.95. 55.27. 55.25. 49.29. 28.32. 19.35. 18.06. 15.80. 15.75. 1H NMR (400 MHz. CDC13) 7.06 i 6.92 (m. 4H). 6.88 (td. J: 817. 4.6 Hz. 2H). .63 (dq. J: 9.6. 6.2 Hz. 1H). 4.99 (d. .1: 7.9 Hz.
(Thin ?lm) HRMS-ESI (/77 Z) 1H). 4.13 (p.J: 6.9 Hz. 3377. 2979, ([M+Na]7) calcd for 1H). 3.91 (d..]= 9.6 Hz. 254 1706. 1513. C25H31F2NNa06, 1H). 3.84 (s. 3H). 3.83 (s. 1274. 1161. 502.2012; found, 3H). 1.42 (s. 9H). 1.22 (d, J 1025. 729 502.2008 = 6.2 Hz. 3H). 0.90 (d, J: 7.2 Hz. 3H). 19F NMR (376 MHz. CDC13) —134.14.—134.59.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.05 (ddd, .7: 7,8, 4.8, 2.3 Hz, 2H), 7.01 (d, J : 2.2 Hz, 2H), 0.70 (t, J: 8.8 Hz, 2H), .08 (dq, .1: 10,1, 0.1 Hz, 1H), 4.98 (d, .1: 7.9 Hz, 1H), 4.12 (ddp, J: 11.8, 7.9, 4.3 Hz, 1H), 3.85 (d,J= 10.2 Hz, 1H), 3.70 (s, 3H), 3.74 (Thin ?lm) HRMS-ESI (m z) (s, 3H), 2,16 (s, 3H), 2.14 (s, 3370, 2978, ([M+Na]_) calcd for 3H), 1.41 (s, 9H), 1.21 (d, J 255 171 1, 1502, C27H37NNaOG, : 0.1 Hz, 3H), 0.82 (d, .7: 1247, 1103, 494.2513, found, 72 Hz, 3H). 1052, 730 494.2515 13CNMR(101 MHz, CDC13) 5 172.87, 150.53, 150.30, 154.94, 133.77, 133.55, 130.40, 130.30, 126.81, 120.38, 120.00, 125.80, 110.05, , 79.58, 73,47, 5031, 55.32, 55.27, 49.28, 28.32, 19.34, 18.15, 10.32, 10.24. 1H NMR (400 MHz, CDC13) 7.04 (d, J: 3.0 Hz, 1H), 0.80 (d, J: 3.0 Hz, 1H), 0.74 (dd, .1: 19.1, 8.9 Hz, 2H), (Thin ?lm) HRMS-ESI(/1Iz) 0.00 (ddd, J: 9.1, 0,3, 3.0 3355,2978, ([M+Na]_) calcd for Hz, 2H), 5.88 (dq, J = 10.0, 256 1712, 1497, NN308, 0.2 Hz, 1H), 5.03 (d, .1: 7.8 161, 526.241 1, found, Hz, 1H), 4.91 (d, J: 10.1 1047, 730 526.2405 Hz, 1H), 4.12 (m, 1H), 3.80 (s, 3H), 3.73 (s, 3H), 3.71 (s, 3H), 3.70 (s, 3H), 1.41 (s, 9H), 1.30— 1.19 (m, 3H), 0.80 (d, J = 7.2 Hz, 3H).
[Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd.
MASS N1VJR No. (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.05 (d, .1: 8.4 Hz, 1H), 6.99 (d, J: 8.3 Hz, 1H), 6.88 (d,J= 2.7 Hz, 1H), 6.81 (d, .1: 2.7 Hz, 1H), 6.63 (ddd, J (Thin ?lm) HRMS-ESI (m 2) : 15.9, 8.3, 2.7 Hz, 2H), 5.63 .m...,;4€;// 3364, 2978, ([M+Na]‘) calcd for (dq,J= 10.0, 6.1 Hz, 1H), 257 ”4., 1710, 1497, C27H3‘NNaO6» 4.99 (d, J: 7.9 Hz, 1H), 4.43 1245, 1160, 494.2513; found, (d, .1: 10.1 Hz, 1H), 3.72 (s, 1045, 730 494.2507 3H), 3.72 (s, 3H), 2.32 (s, 3H), 2.26 (s, 3H), 1.46 4 l.39(m, 10H), 1.30(d, .1: 6.2 Hz, 3H), 0.86 (d, J: 7.2 Hz, 3H). 1H NMR (400 MHz, CDC13) 7.08 4 6.91 (m, 3H), 6.89 4 6.82 (m, 1H), 6.76 (ddd, J: 8.0, 3.8, 1.7 Hz, 2H), 5.76 4 .53 (m, 1H), 5.15 4 5.07 (m, 1H), 5.07 4 4.93 (m, 1H), 4.21 4 4.03 (m, 1H), 3.90 4 3.80 (m, 9H), 3.76 4 3.72 (m, 3H), 1.47 —1.37(m,9H), HRMS-ESI (m z) 1.24 (t, .1: 6.0 Hz, 3H), 1.14 ([M+H]+) (61.1: 6.9 Hz, 1H), 0.86 (d, calcd for J = 7.0 Hz, 2H).
C27H37N08Na, 526.241 1, found, 13C NMR (101 MHz, 526.2405 CDC13)6172.73, 172.19, 152.83, 152.74, 147.49, 147.21, 135.15, 135.02, 134.77, 134.64, 123.63, 123.58, , 120.98, 120.94, 120.51, 120.38, 110.86, , 110.67, 73.58, 60.35, 60.29, 60.20, 55.65, 42.03, 41.98, 28.31, 18.90,18.77,18.52,18.19.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan CmNE.d. \ MP 1R NMR (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.09 4 7.02 (m, 1H), 6.88 4 .74 (m, 3H), 5.70 4 5.59 (m, 1H), 4.95 (d, J: 7.9 Hz, 1H), 4.85 (d, J: 9.7 Hz, 1H), 4.22 4 4.07 (m, 1H), 3.97 (d, J: 2.4 Hz, 3H), 3.86 (d, J: 2.1 Hz, 3H), 1.42 (s, . - 9H), 1.23 (d, .1: 6.2 Hz, SEE“ $191311) 3H), 0.96 (d, J: 7.2 Hz, ,7 ’ HRMS-ESI (mz) 3H). 1715,1618, - ([M+Na] )calcd for. \ 1501 1475 12 259 :4: 1430’ 1293’ F4N06Na, ”C NMR (126 MHz, 1252’ 1165’ 23; found, CDC13)5172.67, 154.91, 1102:1058: 538.1826 151.50, 151.26 (11.5113 Hz), 149.47 (Gui 11.5 Hz), 951’ 748 149.28 (d, J: 11.5 Hz), 147.24, , 147.03, 146.97, 145.35, 145.24, 143.36, 143.25, 129.90 (d,J =35 Hz), 129.59, 123.09— 122.78 (111), 122.38, 110.96 — 110.60 (m), 79.81, 72.19, 61.23, 61.17, 49.21, 42.46, 28.29, 18.87, 18.29.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan CmNE.d. \\ MP IR NMR (0C) (cm'l) (1H,13C,19F) 1H NMR (400 MHz, CDC13) 7.07 4 6.84 (m, 6H), 5.64 (dq,J: 11.9, 5.9 Hz, 1H), 4.96 (d, J: 8.1 Hz, 1H), 4.44 (d, J: 10.3 Hz, 1H), 4.18 — 4.02 (m, 1H), 2.35 (s, 3H), . 2.29 (s, 3H), 2.27 (s, 3H), 3382, 2977),Thm ?lm 2‘25 (3’ 1H) 1‘42 ES” 9H)”a HRMS—ESI (m z) - 1.27 (d, .14 6.1 Hz, 3H), 0.82 2950, 1715,, ([M+Na] )calcd for \ (d J: 7 2H2 3H) 260 1501, 1453, NO4Na, ’ ' ’ ' 167131;365 9 4624253381?“d°~. 2222212221222 * ’ ' , CDC13) 5 172.97, 154.93, 811, 754 , 138.55, 135.43, 135.04, 133.58, 133.35, 130.57, 130.28, 128.58, 127.87, 127.22, 126.90, 79.67, 7472, 4926, 47.36, 34.67, 28.32, 21.26, 21.22, 19.77, 19.73, 18.86.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No. (0C) (cm'l) (H, 13C, 19F) 1H NMR (400 MHz, CDC13) 7.15 (d, .1: 8.5 Hz, 1H), 7.11 (d, J: 8.5 Hz, 1H), 6.96 — 6.88 (m, 4H), 5.64 (dq, J: 9.9, 6.1 Hz, 1H), 4.94 (d, J: 7.9 Hz, 1H), 4.42 (d, .1: 10.0 Hz, 1H), 4.17 — 4.05 (m, 1H), 2.34 (s, 3H), 2.30 (3, (Thin ?lm) 3H), 2.25 (s, 3H), 2.22 (s, 3364, 2977, ([IMHfN‘li?i$21};r 3H), 1.42 (s, 9H), 1.28 (d, J 1713,1499, =62 Hz, 3H), 0.84 (d,J= 26 1 1“: C27H}7N04Na, 1452, 1365,,, 7.1 Hz, 3H).,, :2: :1: 462.261 5, found, 1209,1164, 462 2614 1 1049, 731 ' 13C NMR (126 MHz, 6172.88, 154.95, 136.54, 136.39, 136.19, 136.07, 135.85, 135.52, 131.49, 131.16, , 127.12, 126.82, 126.56, 79.63, 74.68, 49.24, 46.84, 34.67, 31.59, 2832, 20.84, .10, 20.06, 18.94.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No, (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 6 7.11 (dd, .1: 8.4, 6.0 Hz, 1H), 7.07 (dd, J: 8.5, 60 Hz, 1H), 7.00 (dd, J: 10.6, 2.6 Hz, 1H), 6.90 (dd, J: .3, 2.7 Hz, 1H), 6.87 4 6.77 (m, 2H), 5.55 (dq,J= 9.6, 6.2 Hz, 1H), 4.95 (d, J: 7.2 Hz, 1H), 4.45 (dt, .1: 9.6, 1.2 Hz, 1H), 4.20 — 4.08 (m, 1H), 2.34 (s, 3H), 2.28 (Thin ?lm) (s, 3H), 1.42 (s, 9H), 1.31 (d, 3381,2979, HRMS-ESI(I1IZ) J: 6.2 Hz, 3H), 0.89 (d,J: 1711,1609, ([M+Na]_) calcd for 7.3 Hz, 3H). 1589,1495, 262 C25H31F2NO4N3, 1454,1300, 4702113, found, 1\4R(1261\4Hz, 1241,1165, 470.2120 CDC13) 5 172.77, 161.36 (d, 1049, 810, .1: 2439 Hz), 16132 (d, .1: 2435 Hz), 154,96, 14069 (d, J: 6.7 Hz), 14010 (d, J = 6.4 Hz), 132.38 (d,J= 3.2 Hz), 132.07, 132.01, 131.69 (d,J= 7.9 Hz), 114.83 (d,J =22.3 Hz), 114.34 (d,J= 22.2 Hz), 11307 (d, .1: 20.7 Hz), 113.35 (d,J= 207 Hz), 7979, 73.85, 49.16, 47.74, 34.67, 31.59, 28.31, 19.39, 19.35, 18.82, 18.05.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.01 4 6.86 (m, 3H), 6.82 (dd, J: 5.8, 3.1 Hz, 1H), 6.74 — 6.64 (m, 2H), 5.82 (dq,J= 12.0, 6.2 Hz, 1H), 4.97 (d, .1: 7.8 Hz, 1H), 4.67 (d, J: 10.5 Hz, 1H), 4.21 — 4.09 (m, 1H), 3.74 (s, 6H), 1.42 (s, 9H), 1.29 (d, .1: 6.2 (Thin ?lm) Hz, 3H), 0.89 (d, J = 7.3 Hz, 2978, 1710, HRMS-ESI (mt) 3H). 1497, 1454, ]‘) calcd for 263 1366, 1249, C25H31F2N06, 13C NMR (126 MHz, 1209, 1160, 502.2012, found, CDC13) 5 172.70, 156.13, 1036, 814, 11 155.90, 155.74, 155.57, 728 154.90, 154.24, 154.00, 127.94 (d,J= 15.8 Hz), 12763 (d, J: 16.2 Hz), 11624 (d, J: 24.9 Hz), 115.97 (d,J=24.8 Hz), 115.14, 114.12, 1]3.16(d,J : 8.3 Hz), 113.03 (d, .1: 8.2 Hz), 79.69, 71.79, 55.70, 49.15, 43.38, 34.66, 28.30, 19.00, 18.12. ation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan CmNE,d. MP 1R NMR (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.27 (1, .1: 8.6 Hz, 1H), 7.16 (t, J: 8.5 Hz, 1H), 6.65 — 6.50 (m, 4H), 5.82 — 5.72 (m, 1H), 4.96 (d, J: 7.9 Hz, 1H), 4.60 (d, .1: 10.2 Hz, 1H), 4.21 — 4.09 (m, 1H), 3.75 (s, 3H), 3.74 (s, 3H), 1.42 (s, 9H), 1.26 (d, .1: 6.1 297181 $191316). - Hz, 3H), 0.92 (d, J = 7.3 Hz, 1 ,’ HRMS-ESI (m’Z) 3H). 1712, 1623, - ([M+Na] )calcd for. 1585 1506 12 264 C25H31F2N06Na, ”C NMR (126 MHz, 1 44 51 1366’ 1288’ 1159’ 502.2012, found, CDC13) 5 172.73, 161.24 (d, 1031”, 950’” 502.2016 .1: 2457 Hz), 16101 (d, .1: 246.0 Hz), 15975 (d, J: 8347 731 11.1 Hz), 159.50 (d,J= 11.3 Hz), 154.93, 129.86 (61.1: .8 Hz), 129.31, 119.70 (d,J = 14.6 Hz), 119.41 (d,J= .1 Hz), 110.15 (d, .1=2.9 Hz), 109.77 (d, .1: 3.0 Hz), 101.81 (d,J= 26.8 Hz), 79.67, 72.07, 55.51, 49.19, 41.73, 28.31, 19.01, 18.24.
[Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.53 (d, .1: 8.0 Hz, 1H), 7.31 (d, J: 8.0 Hz, 1H), 7.16 (d, J: 7.6 Hz, 1H), 7.14 — 7.10(m, 1H), 7.01 (dd, J: .7, 1.7 Hz, 2H), 6.01 4 .91 (m, 1H), 4.97 (d, J: 9.7 Hz, 1H), 4.93 (d, J: 8.0 Hz, (Thin ?lm) 1H), 4.18 4 4.06 (m, 1H), 2982, 1714, 3.89 (s, 3H), 3.81 (s, 3H), 1507, 1456, “$3?ng212m 141 (s, 9H), 1.23 (d, J: 6.2 1417, 1327, Hz, 3H), 0.83 (d, .1: 7.2 Hz, 1243, 1212,,, F0N00Na, ,, , 3H). 602.1948, found, 1166, 1123, 6021948 q 1033, 860, ‘ 13C NMR (126 MHz, 739 CDC13) 5 172.77, 157.43, 154.92, 132.51, 132.36, 130.03, 129.43, 125.01, 122.84, 117.27 (q, J: 3.9 Hz), 116.99 (q, J: 3.3 Hz), 107,64(q,J=3.0Hz), 107.44 ((1, .1: 4.1 Hz), 79.75, 7176, 55.70, 49.17, 28.29, 18.94, 18.11. v) 0 La) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd.
MASS N1VJR No, (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.39 (dd, J: 8.7, 5.6 Hz, 1H), 7.27 4 7,22 (m, 1H), 7.16 4 7.05 (m, 2H), 6.98 4 6.89 (m, 2H), 5.58 (dq,J= 88,62 Hz, 1H), 4.95 (d, .1: 7.4 Hz, 1H), 4.68 (d, J: 9.1 (Thin ?lm) HRMS-ESI (m/z) Hz, 1H), 4.61 (d, J: 12.4 3355, 2961, ([M+Na]_) calcd for Hz, 1H), 4.53 (d, .1: 12.5 266 1712, 1493, C27H35F2N06Na» Hz, 1H), 4.42 (d, J: 12.3 1366, 1266, 530.2325; found, Hz, 2H), 4.18 4 4.06 (m, 1160, 1095 31 1H), 3.42 (s, 3H), 3.41 (s, 3H), 1.42 (s, 9H), 1.27 (d, J = 6.2 Hz, 3H), 0.90 (d, J: 7.2 Hz, 3H). 19F NMR(376 MHz, CDC13) 4115.52, —11588. 1H NMR (400 MHz, CDC13) 7.40 (dd, J: 87,56 Hz, 1H), 7.24 (dd, .1: 8.7, 5.6 Hz, 1H), 7.13 (t, J: 3.2 Hz, 1H), 7.10 (t, J: 3.2 Hz, 1H), 6.96 4 6.88 (m, 2H), 5.59 (dq, J: 8.7, 6.2 Hz, 1H), 4.98 (d, J: 7.5 Hz, 1H), 4.69 (Thin ?lm) HRMS-ESI (m z) (d, J: 89 Hz, 1H), 4.65 (d, 3356, 2977, ([M+Na]‘) calcd for J: 12.5 Hz, 1H), 4.59 (d,J: 267 1712, 1494, C29H39F2N06Na, 12.6 Hz, 1H), 4.46 (d, J: 1366, 1160, 558.2638; found, 12.5 Hz, 1H), 4.45 (d, .1: 1 1 16, 1096 558.2638 12.6 Hz, 1H), 4.20 4 4.06 (m, 1H), 3.62 4 3.44 (m, 4H), 1.42 (s, 9H), 1.32 4 1.18 (m, 9H), 0.91 (d, .1: 7.2 Hz, 3H).
”P NMR (376 MHz, CDCH) -115,64,-115.97.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.07 (q, .1: 8.0 Hz, 4H), 6.93 (dd, J: 7.7, 3.2 Hz, (Thin ?lm) 2H), 6.85 (t, J = 7.5 Hz, 2H), 3372,2978, 6.74 — 6.62 (m, 4H), 5.65 2936, 2835, HRMEESU’" ‘) (dqd, J : 9.3, 6.1, 3.1 Hz, ([ 1 ) 1713, 1582, 2H), 4.96 (d, J: 7.4 Hz, 1500, 1457, calcd for 1H), 4.81 (s, 1H), 4.60 (dd, J 1366, 1306, C27H37N06Na, : 9.9, 6.0 Hz, 2H), 4.09 (dt, 1257, 1211, 494.2513, found, J: 15.3, 6.9 Hz, 2H), 3.79 1166, 1098, 494.2490 (3, 6H), 3.77 (s, 3H), 3.76 (s, 1048, 910, 3H), 2,27 (d, .1: 7.5 Hz, 752, 734 6H), 2.20 (s, 6H), 1.43 (s, 9H), 1.42 — 1.38 (m, 12H), 1.26 (1, .1: 6.0 Hz, 6H), 0.83 (d, J: 7.2 Hz, 3H). 1H NMR (400 MHz, CDCl;) 8 7.30 (dd, .1: 7.6, 1.4 Hz, . 2H), 7.14 (d,J= 7.7 Hz, 52117“ $17118) 2H), 7,11 — 6.99 (m, 4H), [712’ 1500’ HRMS—ESI (m z) 6.99 4 6.87 (m, 4H), 5.73 4 ’ ’ ([M+H]+) 5.49 (m, 2H), 5.20 (d, J = 7.3 1467, 1452, 1420, 1565,4 Hz, 1H), 5.14 — 4.98 (m, A; calcd for 269 5 a :2 3H), 4.1 1 (s, 2H), 3.81 (8, $51 1250, 1207, N00Na, “E ,, ,, ,, ,, , 3H), 3.76 (S, 3H), 3.74 (S, 1162, 1091, 494.2513, found, , , 1053, 1006,, 3H),).71(s,5H),2.35 — 4942509 2.23 (m, 12H), 1.43 (d, .14, , i 909 866 12.5 Hz, 18H), 1.26(dd,J: 7657 730 6.2, 2.1 Hz, 6H), 1.09 (d,J= 6.8 Hz, 3H), 0.82 (d, .1: 7.1 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. MP 1R NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.31 (d, .1: 8.5 Hz, 1H), 7.11 (d, J: 8.4 Hz, 1H), 6.41 (dt, J = 5.2, 2.6 Hz, 2H), $221 $17116). 6.37 (dt, .1 = 5.6, 2.7 Hz, 2H)” 5 '84 “1‘17 J :3‘8’ 6‘2 2935, 2836, ESIMS m z 521 ([M+NH4]+) Hz, 1H), 5.01 (d, J— 7.9 Hz, 1711 1608 1585’1504’ 1H), 4.79 (d,.]= 9.9Hz, ‘ 1453 ’ 1H), 41844.06 (m, 1H), 3.81 (s, 3H), 3.74 (s, 6H), 3.73 (s, 3H), 1.42 (s, 9H), 1.20 (d, .1: 6.2 Hz, 3H), 0.88 (d, J : 7.2 Hz, 3H). 1H NMR (300 MHz, CDCH) 7,28 (d, J: 7.8 Hz, 1H), 7.13 — 7.03 (m, 1H), 6.69 — . 6.56 (m, 4H), 5.86 (dq, J: S??? $91217) 9.8, 6.2 Hz, 1H), 5.01 (d, J : 271 334’ 1712’ ESIMS m z 489 7.8 Hz, 1H), 4.88 (d, J = 9.9 ’ ’ ([M+NH4]+) Hz, 1H), 4.20 — 3.98 (m, 1611,1504, 1H), 3.81, (S, 3H), 3.7.)a 4 3 (S, 3H), 2.27 (s, 3H), 2,26 (s, 3H), 1.41 (s, 9H), 1.21(d,J : 6.1 Hz, 3H), 0.85 (d, J: 71 Hz, 3H).
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd.
MASS NMR No. (cm ) (1H7 13c:1 19F) 1H NMR (300 MHz, CDC13) 7.18 (d, .1: 2.1 Hz, 1H), 7.03 (d, .7: 2.2 Hz, 1H), 6.95 — 6.88 (m, 2H), 6.73 (d, J: 8.3 Hz, 1H), 6.68 (d, .1: 8.3 (Thin ?lm) Hz, 1H), 5.83 (dq, .7: 12.2, 3366, 2978, 6.1 Hz, 1H), 5.03 (d, J: 7.9 ESIMS m z 489 272 2933, 2835, ([M+NH4]+) Hz, 1H), 4.93 (d, J: 10.3 1714, 1501, Hz, 1H), 4.19 4 4.05 (m, 1453 1H), 3.81 (s, 3H), 3.72 (s, 3H), 2.24 (s, 3H), 2.21 (s, 3H), 1,42 (d, .1: 0.6 Hz, 9H), 1.21 (61,7: 61 Hz, 3H), 0.84 (d, J: 7.2 Hz, 1H NMR (400 MHz, CDC13) 7.05 - 6.93 (m, 2H), 6.91 - 6.75 (m, 4H), 5.71 (dq,./: .1, 6.2 Hz, 1H), 4.91 (d, J = 7.9 Hz, 1H), 4,20 - 4.07 ESIMS 777 Z 480 (m, 1H), 3.96 (d, .7: 10.0 ([M+H]+) Hz, 1H), 3.86 (s, 3H), 3.85 (s, 3H), 1.42 (s, 9H), 1.23 (d, .7: 6.1 Hz, 3H), 0.86 (d, .1: 7.2 Hz, 3H), 19F NMR (376 MHz, CDC13) -13712, -13769, 1H NMR (400 MHz, CDC/17,) 7.22 _ 7.04 (m, 2H), 6.77 _ 6.56 (m, 4H), 5.60 (dq, J = 9.8, 6.1 Hz, 1H), 4,95 (d,J= ESIMS m z 472 7.9 Hz, 1H), 4.36 (d, .1: 10.0 274 ([M+H]+) Hz, 1H), 4.20 — 4.03 (m, 1H), 3.75 (s, 3H), 3.73 (s, 3H), 2.35 (s, 3H), 2.31 (s, 3H), 1.42 (s, 9H), 1.27 (d, J: 6.2 Hz, 3H), 0.87 (d, J: 7.2 Hz, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd.
No1 (cm ) (1H, 13C, 191:) ESIMS m z 432 275 ([M+H]+) 1H NMR (400 MHz, CDC13) 7.35 _ 7.28 (m. 2H), 7.25 _ 7.20 (m. 2H), 7.20 — 7.09 (m. 2H). 6.65 _ 6.51 (m, 2H), .81 (dq. .1: 10.0. 6.2 Hz.
ESIMS 771 Z 432 1H). 4.92 (d, J: 8.0 Hz, 276 ([M+H]+) 1H). 4.53 (d, J: 10.1 Hz. 1H). 4.19 _ 4.04 (m. 1H), 3.83 (s. 3H), 1.42 (s, 9H). 1.23 (d. J: 6.2 Hz. 3H), 0.78 (d, .1: 7.2 Hz. 3H). 19F NMR (376 MHz. CDC13) a -11326. 1H NMR (400 MHz. CDC13) 8 7.33 - 7.20 (m, 5H). 7.19 — 7.10 (m. 1H). 6.92 - 6.81 (m. 2H), 5.75 (dq, J: 10.3, 6.1 Hz. 1H). 4.91 (d. J: 8.0 Hz.
ESIMS 777 Z 416 1H), 4.26 (d, .1: 10.3 Hz, 277 ([M+H]+) 1H). 4.18 - 4.02 (m, 1H), 2.38 (s. 3H), 1.42 (s, 9H). 1.25 (d, .1: 6.1 Hz. 3H). 0.79 (d. J: 7.2 Hz. 3H). 19F NMR (3 76 MHz. CDClg) -11670.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS NMR No. (‘0 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz. CDC13) 7.32 - 7.12 (m. 6H). 6.59 (td. J: 5.3. 2.6 Hz. 1H). 6.52 (dd. J: 10.9. 2.5 Hz. 1H). 5.79(dq..1= 10.1. 6.1 ESIMS m z 432 Hz. 1H). 5.00 (d. .1: 8.2 Hz. 278 ([M+H]+) 1H). 4.51 (d, J: 10.2 Hz. 1H). 4.19 — 4.04 (m. 1H). 3.75 (s. 3H). 1.41 ). 1.21 (d. J: 6.1 Hz. 3H), 0.86 (d. J: 7.2 Hz. 3H).
”P NMR (376 MHz. CDC13) —113.59. 1H NMR (400 MHz. CDC13) 7.35 — 7.15 (m. 6H). 6.90 — 6.77 (m. 2H). 5.72 (dq. J: .1. 6.1 Hz. 1H). 4.97 (d. .1 = 8.4 Hz. 1H). 4.23 (d, J = ESIMS m z 416 .1 Hz. 1H). 4.19 — 4.03 (m. 279 ([M+H]+) 1H). 2.31 (s. 3H). 1.42 (s. 9H). 1.23 (d. J: 6.1 Hz. 3H). 0.82 (d. J: 7.2 Hz. 19F NMR (376 MHz. CDC13) -117.14_ [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS NMR No. (‘0 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.19 (d, .1: 8.0 Hz, 2H), 7,13 (51,1: 8.1, 6.5 Hz, 1H), 7.04 (d, J: 7.9 Hz, 2H), 6.61 _ 6.50 (m, 2H). .78 (dq, .1: 9.7, 6.1 Hz, ESIMS m z 446 1H), 4.94 (d, J: 7.8 Hz, 280 ([M+H]+) 1H), 4.49 (d, J: 9.8 Hz, 1H), 3.82 (s, 3H), 2.26 (s, 3H), 1.42 (s, 9H), 1.21 (d, J = 6.2 Hz, 3H), 0.82 (d, J: 7.2 Hz, 3H). 19F NMR (376 MHz, CDC13) -11347. 1H NMR (400 MHz, CDC13) 7.31 - 7.25 (m, 1H), 7.16 - 7.09 (m, 2H), 7.04 (d, .1: 7.8 Hz, 2H), 6.91 _ 6.80 (m, 2H), .72(dq,J= 102,62 Hz, 1H), 4.92 (d, .1: 8.0 Hz, ESIMS m z 430 1H), 4.22 (d, J: 10.2 Hz, 281 ([M+H]+) 1H), 4.18 — 4.02 (m, 1H), 2.37 (s, 3H), 2.25 (s, 3H), 1.42 (s, 9H), 1.24 (d, J: 6.1 Hz, 3H), 0.83 (d, .1: 7.2 Hz, 19F NMR (376 MHz, CDC13) -116.91.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd.
MASS NMR No. (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.26 (dd, .7: 8.5, 6.5 Hz, 1H), 7.16 (d,J: 8.1 Hz, 2H), 7.06 (d, J: 8.0 Hz, 2H), 6.58 (td, .1: 83,26 Hz, 1H), 6.52 (dd, .1: 10.9, 2.5 Hz, 1H), 5.77 (dq,J= ESIMS m z 446 .1, 6.1 Hz, 1H), 5.01 (d,J 282 ([M+H]+) : 8.4 Hz, 1H), 4.48 (d, .1: .3 Hz, 1H), 4.19 — 4.04 (m, 1H), 3.76 (s, 3H), 2.27 (s, 3H), 1.41 (s, 9H), 1.21 (d, .1 : 6.1 Hz, 3H), 0.85 (d, J: 7.2 Hz, 3H).
"’F NMR(376 MHz, CDC13) -113.81.
'H NMR (400 MHz, CDCH) 7.31 (dd, J: 8.6, 5.8 Hz, 1H), 7.14 — 7.04 (m, 4H), 6.87 — 6.77 (m, 2H), 5.70 (dq,J= 10.1, 6.1 Hz, 1H), ESIMS m 'z 430 4.97 (d, J: 7.8 Hz, 1H), 4.19 ([M+H]+) (d,./: 10.3 Hz, 1H),4.17— 4.02 (m, 1H), 2.31 (s, 3H), 2.28 (s, 3H), 1.42 (s, 9H), 1.22 (d, .1: 6.2 Hz, 3H), 0.81 (d, J: 7.2 Hz, 3H). 19F NMR (376 MHz, CDCH) -11735.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS NMR No, (‘0 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8 7.35 - 7.22 (m, 2H), 7.12 (dd, J: 84,65 Hz, 1H), 6.98 — 6.84 (m, 2H), 6.71 — 6.48 (m, 2H), 5.78 (dq, J: 12.1, 6.3 Hz, 1H), 4.91 (d, .1 ESIMS m z 450 = 8.0 Hz, 1H), 4.49 (d, J: 284 ([M+H]+) 9.9 Hz, 1H), 4.25 — 4.02 (m, 1H), 3.82 (s, 3H), 1.42 (s, 9H), 1.22 (d, J: 6.2 Hz, 3H), 0.84 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) 8 —112.92, —116.53. 1H NMR (400 MHz, CDC13) 8 7.31 - 7.16 (m, 3H), 7.00 - 6.79 (m, 4H), 5.70 (dq, .1: .3, 6.1 Hz, 1H), 4.89 (s, ESIMS m z 434 1H), 4,25 (d, J: 10.2 Hz, 285 // ([M+H]+) 1H), 4.18 _ 4.04 (m, 1H), 2.36 (s, 3H), 1.42 (s, 9H), 1.25 (d, J: 6.1 Hz, 3H), 0.87 (d, .1: 7.0 Hz, 3H). 19F NMR (376 MHz, CDC13) 8 —1]6.06, —116.38.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS NMR No. (‘0 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.25 - 7.19 (m, 3H), 6.99 - 6.90 (m, 2H), 6.60 (td, J: 8.3, 2.5 Hz, 1H), 6.54 (dd, J = 10.9, 2.5 Hz, 1H), 5.74 (dq,.1: 11.9, 6.1 Hz, 1H), ESIMS m z 450 4.94 (d, J: 7.8 Hz, 1H), 4.48 286 ([M+H]+) (d,J= 10.2 Hz, 1H), 4.19 — 4.05 (m, 1H), 3.77 (s, 3H), 1.42 (s, 9H), 1.20 (d, J: 6.2 Hz, 3H), 0.86 (d, J: 7.3 Hz, 19F NMR (376 MHz, CDC13) 8 -113.32, —116.1 1. 1H NMR (400 MHz, CDC13) 7.30 (dd, J: 8,6, 5.7 Hz, 1H), 7.24 _ 7.11 (m, 2H), 7.01 — 6.93 (m, 2H), 6.92 — 6.69 (m, 2H), 5.67 (dq, J: .0, 6.2 Hz, 1H), 4.92 (d, .1 ESIMS m z 434 = 6.4 Hz, 1H), 4.22 (d, J: 287 ([M+H]+) 10.0 Hz, 1H), 4.18 — 401(m, 1H), 2.29 (s, 3H), 1.42 (s, 9H), 1.22 (d, J: 6.2 Hz, 3H), 0.83 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) 6 -11553, -11686. v) La) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No. (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.21 (dd, .1: 8.5, 6.6 Hz, 1H), 7.16 (dd,J: 8.5, 59 Hz, 1H), 6.82 (11,7: 8.4, 4.1 Hz, 2H), 6.59 (1d, .1: 8.2, 2.5 Hz, 1H), 6.53 (dd, .1: HRMS-ESI (m/z) 10.8, 2.4 Hz, 1H), 5.67 (dq, J (Thin ?lm) ([M+Na]_) calcd for = 12.3, 6.1 Hz, 1H), 4.97 (d, 3364, 2978, 288 C25H31F2NN305, .1: 6.5 Hz, 1H), 4.73 (d, .1: 1709, 1600, 486.2063, found, 10.2 Hz, 1H), 4.25 —4.04 1496,1161 486.2063 (m, 1H), 3.78 (s, 3H), 2.42 (s, 3H), 1.42 (s, 9H), 1.21 (d, J: 6.1 Hz, 3H), 0.92 (d,J: 7.2 Hz, 3H).
"’F NMR (376 MHz, CDC13) —113.52, -116.98.
'H NMR (400 MHz, CDCH) 7.32 — 7.27 (m, 1H), 7.23 — 7.14 (m, 1H), 6.81 —6.71 (m, 2H), 6.61 (td, .1: 8.3, 2.5 Hz, 1H), 6.54 (dd, J = 10.8, 2.5 Hz, 1H), 5.79 (dq,J= 11.8, 6.1 Hz, 1H), 4.95 (d, .1 HRMS-ESI (/17 Z) (Thin ?lm) : 7.1 Hz, 1H), 4.76 (d, J: ([M+Na]_) calcd for 3364, 2979, 10.1 Hz, 1H), 4.21 —4.05 289 / F3NN305, Z. 1710, 1601, (m, 1H), 3.76 (s, 3H), 1.42 ”i 490.1812; found, 1501, 1162 (s, 9H), 123 (d, J: 63 Hz, 490.1809 3H), 0.90 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) —1 1215 (d, J: 44.2 Hz), - 112,17 (d,./:44.3 Hz), - 112.91.
[Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.30 (dd, J: 8.4, 6.2 Hz, 1H), 7.03 (dd, J: 8.6, 6.6 Hz, 1H), 6.80 (d, J: 8.7 Hz, 2H), 6.58 (d, J: 9.2 Hz, 2H), 5.65 (dq, .1: 9.9, 61 (Thin ?lm) HRMSEESI (’7’ Z) Hz, 1H), 4.93 (d, J: 6.9 Hz, 5565, 2979,M ([M+Na] ) calcd for 1H), 4.75 (d, J— 9.9 Hz,4 _ 290 CNHWFNNaO; 1709, 1497, 486 21063 found, 1H), 4.18 4 4.04 (m, 1H), 1450, 1160 ‘486 21067 ’ 3.84 (s, 3H), 2.28 (s, 3H), ' 1.42 (s, 9H), 1.24 (d, J: 6.2 Hz, 3H), 0.85 (d, .1: 7.2 Hz, 19F NMR (3 76 MHz, CDCH) 6 -11294, -11745. 1H NMR (400 MHz, CDCl;) 7.30 (dd,./: 8.1, 5.8 Hz, 1H), 7.18 — 7.07 (m, 1H), 6.90 — 6.75 (m, 4H), 5.67 (dq,.1: 11.7, 6.5 Hz, 1H), 4.92 (d, J: 6.7 Hz, 1H), 4.61 (Thin ?lm) HRMS'PSI (m/Z) (d, J = 10.1 Hz, 1H), 4.19 — ([M+Na] ) calcd for 5564, 2980,M 5.95 (m,5 1H), 2.29 (s, 5H),5 291 CuHmFxNNaOd 1711, 1499, 47-41H862f0und’ 1.42 (s, 9H), 1.27 (d, J: 6.3 1163 ‘ 1 ’ Hz, 3H), 0.85 (d, J: 7.2 Hz, 474.1863 191: NMR (376 MHz, CDC13) 6 -1 1 1.50 (d, .7: 7.3 Hz), - 112.52(d,J:7.1 Hz), _ 116.50.
[Annotation] Mel.Chan None set by an [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H. 13C. 191:) 1H NMR (400 MHz. CDC13) for both diastereomers of a 1:1 mixture (1 7,18 - 7.09 (m. 2H). 7.01 — 6.87 (m, 10H). .76 — 5.58 (m, 2H), 5.03 (d.
J: 5.4 Hz, 1H), 5.01 (d, J: (Thin ?lm) 4.9 Hz. 1H), 5.01 — 4.90 (m. 3363, 2979, 2H), 4.20 — 4.06 (m, 2H), 292 2939. 2838, 3.92 (d, J: 2.1 Hz. 3H), 3.89 17121586, (d,J=2.0Hz,3H).3.81(d. 1477 J=1.9 Hz,3H).3.80(d,J= 1.9 Hz. 3H). 1.44 (s. 9H). 1.42 (s. 9H), 1.25 (d, J: 6.6 Hz, 3H). 1.23 (d. J = 6.3 Hz. 3H).1_17(d..1: 7.1 Hz, 3H). 0.90 (d, J: 7.2 Hz, lH NMR (400 MHz, CDClg) major diastereomer of a 2:1 mixture (1 7.15 (dt, J: 9.6. 3.0 Hz. 1H). 6.93 (td, .1: . 8.8, 8.2.3.1Hz.1H), 6.89 — :21:12ng 6.81 (m. 2H), 6.80 — 6.68 (m. 293 5339’ 1712’ 2H). 5.84 (dd. J : 9.6. 6.2 Hz, 1H). 4.98 (s. 1H), 4.86 14957 1455 (d. J: 9.2 Hz, 1H). 4.24 — 4.07 (m, 1H). 3.82 (s, 3H). 3.74 (s. 3H), 1.42 (s, 9H), 1.23 (d. J = 6.3 Hz. 3H), 0.90 (d. .1: 7.2 Hz, 3H).
[Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd.
MASS N1VJR No. (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 6 7.194 7.10 (m, 2H), 7.104 7.07 (m, 4H), 7,03 4 6.98 (m, 1H), 6.98 — 6.92 (m, 1H), .76 (dq, .1: 10.3, 6.1 Hz, 1H), 4.94 (d, .1: 7.9 Hz, 1H), 4.18 — 4.03 (m, 1H), 3.94 (d, .1: 10.3 Hz, 1H), 2.30 (s, 3H), 2.28 (s, 3H), 1.42 (s, 9H), 1.22 (d, J: 6.1 ESIMS m z 412 Hz, 3H), 0.76 (d, J: 7.2 Hz, 294 ([M+H]+) 13C NMR (101 MHz, CDC13) missing one aromatic C signal due to overlap d 172.84, 141.56, 141.27, 138.32, 137.91, , 128.87, 128.60, 128.34, 127.62, 127.30, 125.06, 124,89, 7320, 57.91, 53.39, 49.25, 28.31, 21.46, 21.42, 19.32, 18.01. 1H NMR (400 MHz, CDC13) 7.32 — 7,21 (m, 5H), 7.21 — 7.15 (m, 1H), 6.86 (dd,J= 8.0, 1.7 Hz, 1H), 6.79 (dd, .1 :11.3,1.6 Hz, 1H), 5.85 4 ESIMS m z 416 5.72 (m, 1H), 5.04 — 4.94 (m, 295 ([M+H]+) 1H), 4.39 ((1.1: 10.1 Hz, 1H), 4.14 (p, J: 7.4, 6.8 Hz, 1H), 2.26 (s, 3H), 1.42 (s, 9H), 1.24 (d, .1: 6.1 Hz, 3H), 0.90 4 0.81 (m, 3H). 19F NMR (376 MHz, CDC13) 6 -1 18.88.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No, (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8 7.28 4 7,17 (m, 3H), 6.99 4 6.93 (m, 2H), 6.88 (dd, J: 8.0, 1.7 Hz, 1H), 6.80 (dd, J = 11.2, 16 Hz, 1H), 5.74 (dq, J: 9.9, 6.2 Hz, 1H), ESIMS m z 434 4.98 (d, J: 7.9 Hz, 1H), 4.37 296 +) (d, J: 10.0 Hz, 1H), 4.22 4 4.07 (m, 1H), 2.27 (s, 3H), 1.42 (s, 9H), 1.23 (d, J: 6.2 Hz, 3H), 0.88 (d, J: 7.5 Hz, 19F NMR(376 MHz, CDC13) 8 —1]5.62, —118.85. 1H NMR (400 MHz, CDC13) 7.22 (1, .1: 8.0 Hz, 1H), 7.19 4 7.13 (m, 2H), 7.07 (d, J: 7.9 Hz, 2H), 6.85 (dd,J= 8.0, 1.8 Hz, 1H), 6.77 (dd, J :112, 1.6 Hz, 1H), 5.83 4 ESIMS m z 430 5.69 (m, 1H), 5.03 (d,J= 8.0 Hz, 1H), 4.35 (d, J: 10.3 297 ([M+H]+) Hz, 1H), 4.19 4 4.05 (m, 1H), 2.27 (s, 3H), 2.24 (s, 3H), 1.41 (s, 9H), 1.23 (d, J : 6.1 Hz, 3H), 0.86 (d, J: 8.4 Hz, 3H), 19F NMR (376 MHz, CDC13) 8 4118,95.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd.
MASS NMR No. (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.31 - 7.22 (m, 4H), 7.22 - 7.11 (m, 1H), 7.12 - 7.02 (m, 2H), 6.91 (dd, J: 9.4, 8.2 Hz, 1H), 5.74 (dq, .1: 10.1, 6.2 Hz, 1H), 4.92 (d, .1: 7.9 ,. ESIMS m z 416 ,,/Z.r.’: Hz, 1H), 4.17 _ 4.04 (m, 1H), 4,5,, 298 ([M+H]+) ,,,1! 3.97 (d,J= 10.2 Hz, 1H), f 2.23 (d, .1: 1.9 Hz, 3H), 1.41 (s, 9H), 1,23 (d, J: 6.2 Hz, 3H), 0.76 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) -12018. 1H NMR (400 MHz, CDC13) 7.23 (dd, J: 8,6, 6.6 Hz, 1H), 7.07 _ 7.01 (m, 2H), 6.88 (t, J: 9.3 Hz, 1H), 6.60 (td, J: 8,3, 2.6 Hz, 1H), 6.54 (dd, .1: 109,25 Hz, 1H), 5.72 (dq, J: 11.8, 6.0 ESIMS m z 464 Hz, 1H), 4.95 (d, J: 8.0 Hz, 299 ([M+H]+) 1H), 4.44 (d, .1: 10.3 Hz, 1H), 4.19 - 4.07 (m, 1H), 3.78 (s, 3H), 2.22 (d, J: 1.9 Hz, 3H), 1.42 (s, 9H), 1.20 (d, J: 61 Hz, 3H), 0.86 (d, J: 7.2 Hz, 3H).
”P NMR (376 MHz, CDC13) —113.49, —120.41.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No, (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 7.24 (dd, .1: 9.6, 5.6 Hz, 1H), 7.16 (t, J: 7.9 Hz, 1H), 6.85 (dt, J: 10.4, 2.4 Hz, 3H), 6,79 (dt, .1: 1 1,3, 1.1 Hz, 1H), 5.70 (dq, .1: 10.2, ESIMS 777 Z 448 6.2 Hz, 1H), 4.99 (d, J: 8.0 ([M+H]+) Hz, 1H), 4.61 (d, J: 10.1 Hz, 1H), 4.22 4 4.09 (m, 1H), 2.39 (s, 3H), 2.26 (s, 3H), 1.42 (s, 9H), 1.25 (d, J : 6.1 Hz, 3H), 0.92 (d, .1: 7.2 Hz, 3H) 19F NMR (376 MHz,CDC13) 6 —116.47, 0. 1H NMR (400 MHz, CDCl;) 7.30 4 7.21 (m, 2H), 6.92 4 6.85 (m, 1H), 6.85 4 6.74 (m, 3H), 5,84 4 5.73 (m, 1H), 4.97 (d, .1: 7.9 Hz, 1H), 4.68 (d, J: 10.0 Hz, 1H), 4.22 4 ESIMS m z 452 4.07 (m, 1H), 2.28 (s, 3H), ([1V1+H]+) 1.42 (s, 9H), 1.26 (d, .1: 6.2 Hz, 3H), 0.90 (d, J : 73 Hz, ”P NMR (376 MHz, CDC13) -11163 (d,J= 7.5 Hz), 4 112.07 (61,]: 7.0 Hz), 4 118,16.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No, (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.29 4 7.21 (m, 4H), 7.19 4 7.13 (m, 3H), 7.09 (d, J: 7.9 Hz, 2H), 5.77 (dq, J: 10.3, 6.1 Hz, 1H), 4.92 (d, .1 : 7.9 Hz, 1H), 4.17 4 4.04 (m, (Thin ?lm) 1H), 3.99 (d, J: 10.3 Hz, 3366, 2979. Wilfg?ff”) 1H), 2.28 (s, 3H), 1.41 (s, 2932, 1713, 9H), 1.23 (d, .1: 6.1 Hz, 1496, 1452, calcd for 3H), 0.75 (d, J = 7.2 Hz, 1365, 1306, C24H32NO4, 3H). 1248, 1211, 398.2326; found, 1165, 1053, 398.2328 13C NMR (126 MHz, 699 CDC13) 5 172.83, 154.94, 141.81, 138.26, 136.50, , 129.46, 128.47, 127.93 (d, J: 3.6 Hz), , 120.94, 79.63, 73.17, 57.62, 49.18, 34.67, 28.31, 20.97, 19.30, 18.00.
'H NMR (400 MHz, CDC13) 7.26 (d, J: 4.5 Hz, 5H), 7. 18 (d, J = 7.9 Hz, 2H), 7.05 (d, .1: 7.9 Hz, 2H), 5.77 (dq, J: 10.0, 6.2 Hz, 1H), 4.94 (d, J: 7.9 Hz, 1H), 4.18 — 4.05 (m, 1H), 3.99 (d, J: HRMS-ESI (/17 Z) (Thin ?lm) 10.0 Hz, 1H), 2.26 (s, 3H), ([M+H]+) 3371, 2978, 1.42 (s, 9H), 1.22 (d, J = 6.2 2931, 1712, calcd for Hz, 3H), 0.80 (d, .1: 7.2 Hz, w 0 Lu ~11",<[4.11n. 1495, 1451, C24H32NO4, 3H). 1365, 1165, 398.2326, found, 1051, 699 3982324 13CN1\4R(126 MHz, CDC13)6172.83, , 141.52, 138.41, 136.15, 129.12, 128.73, 128.21, 128.05, 127.95, 126.79, 124.35, 79.63, 73.17, 57.47, 49.21, 34.67, 28.31, .94, 19.30, 18.08.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan CmNE,d. MP IR NMR (0C) (cm'l) (H 13C, 191:) 1H NMR (400 MHz, CDC13) 7.25 i 7.20 (m, 2H), 7.15 (d, J: 8.1 Hz, 2H), , J: 7.9 Hz, 2H), 6.96 (1, J: 8.7 Hz, 2H), 5.72 (dq, J: 9.7, ()2 Hz, 1H), 4.93 (d, .1: 7.9 Hz, 1H), 4.17 — 4.06 (m, 1H), 3.99 (d, J: 9.8 Hz, (Thin?lnv 335212271‘51?’6‘é‘i‘23‘ 3371, 2979, HRMS-IESI (m/Z) 3H)” 0'81 (d1 J: 7‘2 HZ’ 2932, 1712, ([M+Na] )calcd for ’ ' 51% ‘ ’ " )‘ 304 1508, 1452, C24H30FNO4Na, 1366 1222 4382051 f n ; 1160710537 50211 d? LCNMRW6 MHZ’ 8116 1 CDC13)5172.80, 16165 (d, J: 2455 Hz), 154.94, 138.13, 137.32 (d,J=3.2 Hz), 136,35, 12952 (d, J: 7.9 Hz), 129.22, 127.89, 126.12 (d,J= 7.8 Hz), 115.56 (d,J= 21.3 Hz), 7968, 73.01, 56.60, 49.19, 34.67, 31.59, 28.31, 20.95, 19.22, 18.07.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan ed set by Mel.Chan Cmpd. \‘ MP IR NMR No. (0C) (cm'l) (1H. 13C. 191:) 1H NMR (400 MHz. CDC13) 8 7.31 4 7.23 (m. 7H). 6.98 4 6.92 (m. 2H). 5.75 (dq, J: .0. 6.2 Hz. 1H). 4.91 (d. J = 7.8 Hz. 1H). 4.18 — 4.07 (m. 1H). 4.02 (d. J: 10.0 (Thin ?lm) Hz. 1H). 1.42 (s. 9H). 1.23 3371. 2979. (d. J: 6.2 Hz. 3H). 0.83 (d. \ 2933. 1710. ESI?€§4:’HZF)02~2 .1: 7.2 Hz. 3H). 305 1509. 1452. :‘> 1366. 1222. 13C NMR (126 MHz. 1160.105]. CDC13)5 172.80. 161.61 (01. 699 .1: 2452 Hz). 154.93. 141.02. 137.26 (d.J=3.4 Hz). 129.55 (d. .1: 7.9 Hz). 128.86. 127.99. 127.05. 115.29 (d.J=21.2Hz). 79.74. 73.05. 57.10. 49.18. 34.67. 28.31. 19.29. 18.12.
La) [0 La) [Annotation] an None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.26 4 7.21 (m, 2H), 7.14 (d, J: 8.2 Hz, 2H), 7.09 (d, J: 8.1 Hz, 2H), 6.98 — 6.90 (m, 2H), 5.73 (dq, J: 10.2, 6.1 Hz, 1H), 4.91 (d, .1: 8.0 Hz, 1H), 4.17 — 4.06 (m, 1H), 3.98 (d, J: 10.2 Hz, (Thin ?lm) 1H), 2.29 (s, 3H), 1.42 (s, 3371, 2979, 9H), 1.22 (d, J: 6.1 Hz, 2932, 1712, 3H), 0.82 Ed, J: 7.2 Hz, ESIMS m Z 4382 306, 1509, 1452, ([M+Na]+) 3H). 1366,1222, 1161,1052, 13CN1\4R(1261V1Hz, 815 CDC13)6172.80, 161.56 (d, J : 245.0 Hz), 154.93, 138.04, 137.58(d,J=3.3 Hz), 136.69, 129.54, 129.43 ((1, J: 7.8 Hz), 127.82, 115.25 (d,J=21.2 Hz), 79.72, 73.11, 56.76, 49.18, 34.67, 28.31, 20.97, 19.28, 18.12.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Chnpd. 0g, REP DR P?y?k No. (0C) (cm'l) (1H. 13C. 191:) 1H NMR (400 MHz, CDC13) 8 7.33 4 7.24 (m, 5H), 7.22 4 7.14 (m, 111), 6,86 4 6.73 (m, 2H), 5.84 4 5.72 (m, 1H), 4.90 (d, J: 8.0 Hz, 1H), 4.40 (d, .1: 10.2 Hz, 1H), 4.18 4 4.05 (m, 1H), 1.42 (s, 9H), (Thin ?lm) HRMS-ESI (m z) 1.26 (d, J: 6.1 Hz, 3H), 0.78 3370, 2980, ([M+H]+) (d, J: 7.2 Hz, 311). § 712’ cdcdibr 1~ 307 1503, 1453, ”C NMR (126 MHz, C3~H7 ENC :: 1366, 1 I64, 42019811611146 CDC13) 5 172.74, 162.98 4 1053, 966, 161.09 (m), 160.06 (dd, J4 420.1995 851,698 169.5, 12.1 Hz), 154.93, 140.15, 129.79, 128.61, 128.22, 127.00, 124.39 (d,J =18.6Hz),111.62(d,J= 19.5 Hz), 104.70 4103.41 (m), 79.71, 72.30, 49.40, 49.15, 34.67, 28.31, 18.97, 17.99.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan CmNE.d. MP 1R NMR (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 6 7.25 4 7.20 (m, 1H), 7.18 (d, J: 8.1 Hz, 2H), 7.07 (d, J: 7.6 Hz, 2H), 6.85 — 6.72 (m, 2H), 5.76 (dtd, .1: 9.5, 6.8, 5.5 Hz, 1H), 4.92 (d, .1: 7.8 Hz, 1H), 4.36 (d, J: 10.0 Hz, 1H), 4.19 — 4.01 (m, . - lH,2.27 (Thm ?lm) 911)), 1.25((d, J=) 6.2 H(z,s,3H,1.42 s, 3364, 2980, HRMS-IESI (m/Z) 3H) 0 82 (d J: 7 2 HZ 2933, 1713, ([M+Na] )calcd for ’ ' ”Ii ‘ ’ " )‘ 308 1502, 1453, C24H26F2NO4Na, 11306563, 1916664, 96519ggund, 13C NMR (126 MHZ, 850 ° ‘ CDC13)6172.74, 161.98 (dd,J: 167.8, 11.9 Hz), 160.01 (dd,J=167.8, 11.9 Hz), 154.93, 137.05, 136.57, 129.90, 129.24, , 124.66 (d,J=11.5 Hz), 11157 (d, J = 20.4 Hz), 104.69 4 102.95 (m), 79.70, 72.38, 49.18, 48.94, 28.31, .97, 18.97, 18.07.
[Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. 5333;, MP IR NMR No, (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 7.29 4 7.19 (m, 3H), 6.99 4 6.93 (m, 2H), 6.86 4 6.75 (m, 2H), 5.81 — 5.70 (m, 1H), 4.90 (d, J: 7.9 Hz, 1H), 4.37 (d,.]: 10.1 Hz, 1H),4.214 . 4.06 (m, 1H), 1.42 (s, 9H), gang? 1.26 (d, J = 6.2 Hz, 3H), 0.85 ‘ ‘ 1 ’ HRMS—ESI (m z) (dd, .1: 7.8, 1.1 Hz, 3H). 1711, 1604, - ([M+Na] )calcd for ;\ 1502 1454 1‘ 309 C23H26F3NO4Na, ”C NMR (126 MHz, 1,) 8 07 1366’ :3 {224‘ 1161’ 460.1706; found, CDC13) 5 172.71, , 10531 966’ 460.1712 162.71, 161.37, 161.28, 8511 ’ 160.87, 160.75, 159.39, 1 159.30, , 135.92, 12976 (d, J: 7.7 Hz), 115.44 (d, J: 21.3 Hz), 11171 (d, .1: 180 Hz), 104,71 4 103.96 (m), 79.80, 72.20, 49.16, 48.78, 34.67, 28.30, 18.99, 18.09.
HRMS-ESI(/1Iz) ([M+H]+) calcd for C26H38N02, 396.2897, found, 396.2896 1H NMR (400 MHz, Acetone—d6) 5 7,3] 7 7.21 (m, 4H), 7.15 (ddd,.l: 10,9, HREEEEJ” Z) 8.5, 2.5 Hz, 4H), 5.87 (dq, J = 10.0, 6.0 Hz, 1H), 4.05 (d, calcd for .1: 10.5 Hz, 1H), 3.85 (q, .1: :: C24H34N02, 7.2 HZ, 1H), 3.31 (dt, J: 368.2584, found, 33, 1.7 Hz, 3H), 2.91 — 2.73 3682584 (m, 2H), 1.26 (d, .1: 6.1 Hz, 3H), 1.19 (1,]: 6.7 Hz, 12H), 0.81 (dd, J: 7.3, 2.8 Hz, 3H).
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd. MP 1R NMR No. (CC) (cm'l) (1H, 13C, 191:) HRMS-ESI (m/z) ([M+H]+) calcd for 340.2271; found, 340.2273 1H NMR (400 MHz, Acetone—d6) 5 7.34 (dd, ./ : 8.7, 5.7 Hz, 1H), 7.26 (dd, J = 8.7, 5.8 Hz, 1H), 7.02 HRMS-ESI(/11z) 6.80 (m, 5H), 5.75 (dq, J: ([M+H+] ) 98,6.1Hz, lH,4.59 d,J: 9.8 Hz, 1H), 3.96 (q, J: 7.2 called for 313 Hz, 1H), 3.72 7 3,60 (m, C211H24F2N02, 2H), 2.40 (s, 3H), 2.37 (s,3 3 ,48 1770. f3 nd ‘348 1778?)” 7 3H), 1.34 (d, J: 6.2 Hz, ' 3H), 1.03 (d, .1: 7.3 Hz, 191: NMR (376 MHz, Acetone) 6 —l [9,66, —l20.05.
ESIMS m z 320 3 14 ([M+H]+) ESIMS 777 Z 320 315 ([M+H]+) ESIMS m 2 380.5 316 ([M+H]+) ESIMS 777 Z 374.4 317 ([M+H]+) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No, (0C) (cm'l) (1H, 13C, 191:) 1:“. ESIMS m z 298 \ + 318 ([M+H], ) ESIMS m z 334 319 £315 ([M+H] ) ESIMS m Z 420 320 ([M+H]+) ESIMS :33‘ 777 Z 428 321 ([M+H1+) 58511“ 117210)Th' f1 HRMS—ESI(I11Z) 7 7 + ([Mm] ) 1494, 1451, 1253, 1231, calcd for 1204, 1 1 17, ClegzNog, 1080, 1046, 45, found, 871, 746, 44 ESIMS 777 Z 4123 .tx‘ + ESIMS m 2 408.4 324 ([M+H]+) ESIMS m 2 440.3 325 ([M+H]+) ESIMS m 2 400.4 326 ([M+H]+) [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No (CC) (cm'l) (H, 13C, 191:) ESIMS m z 404 327 ([M+H]+) ESIMS m z 372 328 ([M+H]+) ESIMS m z 372 329 ([M+H]+) ESIMS m z 380 330 ([M+H]+) ESIMS m z 380 33 1 ([M+H]+) ‘H NMR (500 MHz, Methanol-d4) 8 6.74 (dddd, J = 17.6, 8.0, 3.7, 1.8 Hz, 4H), 6.58 (ddt, .1: 12.2, 10.0, 2.3 Hz, 2H), 5.83 (dq, J : 10.2, Wiggl?m/Z) 6.1 Hz, 1H), 4.13 (d, J = 10.3 ([ 1 ) Hz, 1H), 3.93 (q, .1: 7.2 Hz, calcd for 1H), 3.78 (s, 3H), 3.77 (s, C20H24F2NO4, 3H), 1.28 (d, J: 6.2 Hz, 380.1668, found, 3H), 1.00 (d, J: 7.3 Hz, 3H) 380. 1649 (NH protons not observed). 191: NMR (471 MHz, Methanol—d4) 5 -1 12.85 (t, J = 10.0 Hz), —113.22 (t,J= .3 Hz). v) La) 0 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan . \ MP IR NMR (0C) (cm'l) (H 13C, 191:) 1H NMR (500 MHz, Methanol—d4) 6 6.51 (dd, J: HRMS—ESI (m z) 5.2, 2.3 Hz, 4H), 6.35 (dt, J ([M+H]+) = 13.0, 2.2 Hz, 2H), 5.82 (dq,J= 10.4, 6.1 Hz, 1H), 333 3.99 (d, J: 10.4 Hz, 1H), C C??fg «1 3.89 (q,J= 7.2 Hz, 1H), 3.75 404 222063;? £63m ‘404 21038 ’ (s, 6H), 3.74 (s, 6H), 1.27 (d, ' ./:6.2 Hz, 3H), 0.96 (d, .1: 7.3 Hz, 3H) (NH protons not observed). 1H NMR (500 MHz, Methanol-d4) 5 6.75 (d, J = 4.0 Hz, 2H), 6.69 (dt, J: HRMS-ESI(/1Iz) 6.6, 1.9 Hz, 2H), 6.61 (s, ([M+H]+) 1H), 6.58 (d, J: 2.3 Hz, 1H), 5,82 (dq, .1: 10.4, 6.1 334 \ Hz, 1H), 3.97 (d, J: 10.5 C C??fg :5 Hz, 1H), 3.85 (q, J = 7.3 Hz, 372 2221633, £0311d ‘372 21146 ’ 1H), 3,75 (s, 3H), 3.74 (s, ‘ ' 3H), 2.29 (s, 3H), 2.27 (s, 3H), 1.25 (d, J: 6.2 Hz, 3H), 0.92 (d, J = 7.2 Hz, 3H) (NH protons not observed). 1H NMR (500 MHz, Methanol—d4) 6 6.75 (d, J: 4.0 Hz, 2H), 6.69 (dt, J: HRMS-ESI (m/Z) 6.6, 1.9 Hz, 2H), 6.61 (s, ([M+H]+) 1H), 6.58 (d, .1: 2.3 Hz, . 1H), 5.82 (dq, .1: 104,61 335 \ Hz, 1H), 3.97 (d, J: 10.5 C C3??? ::~: Hz, 1H), 3.85 (q, J: 7.3 Hz, 372 222163 fodnd ’ 1H), 3.75 (s, 3H), 3.74 (s, 3,72 2146 ' 3H), 2.29 (s, 3H), 2.27 (s, 3H), 1.25 (d, J: 62 Hz, 3H), 0.92 (d, .1: 7.2 Hz, 3H) (NH protons not observed).
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS NMR No. (‘0 (cm ) (1H7 13c:1 19F) 1HNMR(500 MHz, Methanol-d4) 5 7.03 (dd, .1: 11,9, 7.5 Hz, 2H), 6.92 2 6.80 (m, 4H), 5.88 (dq, .1: ESIMS m 2 372.1 .5, 6.1 Hz, 1H), 4.05 (d, .1 VJ La) 0‘ ([M+H]+) :104 Hz, 1H), 3.88 (q, .1: 7.2 Hz, 1H), 3.80 (d, J: 1.0 Hz, 6H), 2.12 (s, 3H), 2.11 (s, 3H), 1.26 (d, .1 : 6.1 Hz, 3H), 0.90 (d, .1: 7.2 Hz, 3H) (NH protons not observed). 1H NMR (500 MHz, ol-d4) 5 7.15 — 7.06 (m, 4H), 7.03 (q, .1: 8.5 Hz, 2H), 5.77 (dq, .1: 10.1, 6.2 HRMS-ESI (m/z) Hz, 1H), 4.06 (d, J: 10.0 ([1v1+H]+) Hz, 1H), 3.93 (q, .1 : 7.3 Hz, »\»\ 1H), 3.83 (s, 3H), 3.82 (s, calcd for Lu Lu \1 3H), 1.25 (d, J: 6.1 Hz, C20H24F2NO4, 3H), 1.00 (d, .1: 7.3 Hz, 3H) 68; found, (NH protons not observed). 380.1667 191: NMR (471 MHz, Methanol—d4) 5 8 (dd, 1: 12.6, 8.5 Hz), —136.53 (dd, .1: 12.6, 8.9 Hz). 1H NMR (500 MHz, Methanol-d4) 5 7.14 — 7.03 (m, 4H), 6.80 (dd, .1 : 12.7, 8.4 Hz, 2H), 5.77 (dq, .1 : ESIMS m 2 372.1 10.3, 6.2 Hz, 1H), 3.92 (d, .1 =10.4 Hz, 1H), 3.86 (q, .1: b) b) 00 ([M+H1+) 7.2 Hz, 1H), 3.78 (s, 3H), 3.76 (s, 3H), 2.15 (s, 3H), 2.14 (s, 3H), 1.23 (d,J= 6.1 Hz, 3H), 0.92 (d, J: 7.3 Hz, 3H) (NH protons not observed). v) La) [\J [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (500 MHz, Methanol—d4) 8 7,03 (d, J: 3.0 Hz, 1H), 6.90 4 6.80 (m, HRMS-ESI (m/Z) 3H), 6.75 (ddd, J = 8.9, 4.5, ([M+H]+) 3.1 Hz, 2H), 5.99 (dq, J = .2, 6.2 Hz, 1H), 4.91 (d, J calcd for 339 = 10.2 Hz, 1H), 3.89 (q,J= C H“ N0 3 22 0 6’ 7.2 Hz, 1H), 3.81 (s, 3H), 404.2068, found, 3.73, , (5, 3H), 3.73, , , (S, 3H),, 404 2059' 3.70 (s, 3H), 1.24 (d, J = 6.2 Hz, 3H), 0.97 (d, J = 7.2 Hz, 3H) (NH s not observed). 23310171211112) HRMS—ESI (m z) ’ ’ (1M+H1+) 1617,1501, \ 1473, 1429, calcd for , 1293, 1233, C20H22F1N01, 1189, 1119, 416.1479, found, 1050, 950, 4161479 (Thin ?lm) HRMS-ESI (m’z) 2866, 1742, ([M+H]+) 1500, 1454, ca C1 d for 341 \ 1378, 1226, CBHWNOL 1113, 1048, 340.2271, found,, 808 7,92 1, ’ 69 5863,Thin ?lm1748), HRMS-ESI+(m z) ([M+H] ) 1736, 1526, 1500, 1456, calcd for 1376, 1238, C22H30N02, 1187, 1116, 340.2271, found, 1048, 810, 340.2274 791, 751 La) La) La) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. \ MP 1R NMR No, (0C) (cm'l) (1H,1"C, 191:) (Th'1“ 1m)f1 HRMS-ESI(m'z) 2878, 1751, , ([Mm1 ) 2,, 1738, 1587, \ 1526, 1494, calcd for 1459, 1240, C20H24F2N02, 1226, 1188, 348.1770; found, 1130,1048, 348.1771 811, 754 (Thin ?lm) SI (m z) 2962, 1747, ([M+H]+) 1596, 1497, calcd for 344’3 \‘ 1234, 1205,'3 C20H24F2NO4, 1114, 1052, 380.1668; found,, 1034, 829,5 ",8016“ 811,713 ' ‘ £832)“ 117:2Th' f1 FIRMS—13810112) 7 7 + ([Mm] ) 1622, 1583, 1506, 1444, calcd for 3,45 931; 1287, 1254, CZUHNFZNOn 1193, 1116, 380.1668; found, 1050, 1030, 1 872,833 £94311 117212)Th' f1 HRVIS-ESI (m z) 1 7 + ([NHH] ) 1615, 1588, 1457, 1417, calcd for 1326, 1241, C22H24F6NO4, 1171, 1116, 480.1604; found, 1032, 873, 480.1607 859,740 ESIMS m 2 408.2 347 ([M+H1+) La) La) 4; [Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. n . :\§» \9\\ ‘\‘\3 MP No5 \'\'\x \ §‘_.\\ (‘0 (1H, 13C1 19F) ESIMS m z 4362 ([M+H]+) ESIMS m z 404.] ([M+H]+) ESIMS/172 372.1 ([M+H]+) ESIMS m 2 372.1 3 5 1 ([M+H]+) ESIMS m z 3 80 3: + 352 ([M+H]) ESIMS m z 3 72 i: ([M+H]+) ESIMS m z 332 ([M+H +) :3 ESIMS m z 316 1‘ + 355 ([M+H] ) ESIMS m z 332 355 ‘5 (Wm?) ESIMS m z 316 ([M+H]+) La) La) L11 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by an Cmpd. n . :\§» \\\\\ ‘\‘\3 MP No3 \'\'\x \ §‘_-‘\ (‘0 (1H, 13C, 191:) ESIMS m z 346 358 ii ([M+H]+) ESIMS m z 330 359 (mm +) ESIMS m z 346 360 ([M+H]+) ESIMS m z 350 ([M+H]+) ESIMS m z 334 ([M+H]+) ESIMS m z 350 363 ([M+H]+) ESIMS m z 334 364 ([M+H +) ESIMS mw’z 3 6 S 312([M+H]+) ESIMS m 2 364.2 ([M+H]+) ESIMS/172 368.2 ([M+H]+) La) La) 0 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. n . :\k \v\\ ‘\‘\A MP No‘ (0C) (cm 1) (H 13C, 191:) ESIMS m 2 364.2 368 ([M+H]+) ESIMS m z 3522 369 ([M+H]+) ESIMS m z ?W?22;;61// 3 16([M+H]+) ESIMS m z 334([M+H]+) ESIMS m z 330 ([M+H]+) ESTMS m z 348([M+H]+) ESIMS m z 352 22926283 ([M+H]+) ESIMS m z 316 ([M+H]+) ESIMS m z 364 w,/’/.‘/ T.’ ([M+H]+) mg,”’ ,1 Lin La) La) \] [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No, (0C) (cm'l) (1H,13C, 191:) (Thin ?lm) HRMS-ESI (m/Z) 3408, 2920, ([M+H]+) 1740, 1512, cam for, 377 1495, 1452, i C19H24N02, 1232, 1198,'5 298.1802,_ found, 1114, 1048, 2981798 734,699 ' $7117“ {171219) HRMS—ESI (m z) ’ " ([M+H]+) .11, 1599, 1515, 1493, 1452, calcd for *378 1 1228, 1193, C19H21N02, 1139, 1119, 02; found, 1055, 744, 298.1795 (Thin ?lm) HRMS-ESI (m z) 2879, 1747, +) 1602, 1508, ca C1 d for 379 1454, 1227, 1197, 1116, CWHBFNOZ’ 316.1707; found,, 1053 814 ;, ’ 316.1703 (Thin ?lm) P11113513??? Z) 2896, 1741, 1604, 1509, calcd for 1453, 1226, C18H21FN02, 1117, 1047, 302.1551, found, 732, 699 302.1548 (Thin ?lm) W151i??? Z) 1603, 1509, calcd for *381 s; 1459, 1229, C19H23FNOZ, 1117, 1049, 316.1707; found, 813 316.1705 La) La) 00 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No, (0C) (cm'l) (1H, 13C, 191:) ET?“ ?ll?) HRMS-ESI (m 2) 33 6, 2936, ([N1+H]+) 1743, 1619, 1602, 1503, calcd for 1454, 1235, CmHzoFgNOz, 1208, 1 145, 320.1457, found, 1116, 966, 320.1451 850,699 (Thin ?lm) HRMS-ESI (m z) 3440, 2924, ([M+H]+) 1743’ 1603’ calcd for 383 1502, 1234, C19H22F2N02, 1208, 1116, ,, , 334.1613; found, 1100, 1083, 334.1606,, 9667 849 (Thin ?lm) W151i???” 3384, 2935, 384 : 1743, 1603, calcd for ;j\-; 1503, 1228, F3N02, 1 1 17, 966, 338.1362, found, 850 56 (Thin ?lm) HRIEEEES" Z) 3384, 2935, 1743, 1603, calcd for if: 1503, 1228, C18H10F3N02, 1117, 966, 338.1362, found, 850 338.1356 La) La) 0 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS NMR No, (‘0 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 51205017: 0.6 Hz, 1H), 8.31 (61, J: 8.0 Hz, 1H), 7.97 (d,J= 5.2 Hz, 1H), 7.22 (dddd, J: 11.7, 85, 5.3, 2.6 Hz, 4H), 7.02 4 6.89 (m, 4H), 6.86 (d, J: 5.2 Hz, 1H), 5.72 (dq, J = 9.7, 6.2 Hz, 1H), 4.60 4 4.46 (m, HRMS-ESI(/1Iz) 1H), 4.05 (d, J: 9.8 Hz, ([M+H]+) 1H), 3.94 (s, 3H), 1.24 (d, J calcd for : 6.2 Hz, 3H), 1.06 (d, .7: C25H25FZN2057 7.2 Hz, 3H) 28; found, 471.1726. 13CNMR(101 MHz, CDC13)6171,56, 168.60, 162.98, 162.87, 160.54, 160.42, 155.41, 148.75, 140.43, 136.83, 136.80, 136.73, 136.70, , 129.54, 129.46, 115.83, 115.62, 115.50, 115.29, 109.46, 7332,5614, 56.08, 4787,3092, 19.12, 17.67.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] an Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No, (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 12.08 (01, J: 0.7 Hz, 1H), 8.20 (d, J: 8.0 Hz, 1H), 7.99 (d, J: 5.2 Hz, 1H), 7.24 — 7.13 (m, 4H), 7.03 — 6.93 (m, 2H), 6.93 4 6.84 (m, 3H), .69 (dq, J: 9.1, 6.2 Hz, 1H), 4.59 — 4.45 (m, 1H), 4.05 (d, .1: 9.0 Hz, 1H), 3.96 111113151??? Z) (s, 3H), 1,34 (d, J = 72 Hz, 3H), 1.22 (d, J: 6.2 Hz, calcd for , 3H).
Czs?stZNZOS, 471.1723, found, 13C NMR (101 MHz, 471.1726. CDC13)6171.26, 168.55, 162.94, 16284, 160.49, 160.40, 155.44, 148.78, 140.44, 136.82, 136.79, 136.46, 136.43, , 129.74, 129.67, 129.65, 129.57,115.76,115.55, 115.46, 115.24, 109.50, 99.99, 73.34, 56.11, 55.66, 47.80, 18.95, 17.74.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (500 MHz, CDC13) 812.05(s, 1H), 8.32 (d, J: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.24 (dd, J: 8.7, .8 Hz, 1H), 7.14 (dd, J: 8.6, 5.8 Hz, 1H), 6.92 4 6.72 (Thin ?lm) HRIESIEES’” Z) (m, 5H), 5.64 (dq, J: 9.8, 3371,2981, 6.2 Hz, 1H),4.53 (p,J= 7.3 1735, 1649, calcd for Hz, 1H), 4.44 (d, J : 9.7 Hz, 5388 1495, 1261, C27H29F2N205, 1H), 3.94 (S, 3H), 2.38 (S, 954, 800, 499.2039, found, 3H), 2.31 (s, 3H), 1.31 (d, J 728 499.2044 : 6.1 Hz, 3H), 1.10 (d, J: 7.2 Hz, 3H). 19F NMR (471 MHz, CDC13) 8 —1 16.46 (td, J: 88,57 Hz), -116.87 (td,J= 9.0, 5.9 1H NMR (500 MHz, CDC13) 512.12(s,1H),8,38(d,J= 7.9 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.29 (d, J = 8.3 Hz, 2H), 7.25 (s, 6H), 6.86 (d, J : 5.2 Hz, 1H), 5.80 (dq, J: .3, 6.2 Hz, 1H), 4.48 (p, J = 7.3 Hz, 1H), 3.98 (d, J: (Thin ?lm) WISE???" Z) 10.3 Hz, 1H), 3.93 (s, 3H), 3370, 2962, 1.28 4 1.25 (m, 12H), 1.24 1735, 1649, calcd for (s, 9H), 0.83 (d, J: 7.2 Hz, 1527, 1264, C33H43N205, 3H). 1145, 801, 547.3166, found, 729 547.3163 13C NMR (126 MHz, CDC13)5171.76, 168.50, 155.32, 149.63, 149.44, , 140.42, 138.71, ,130.51,127.66, 127.63, 125.64, 125.36, 109.37, 74.03, 57.25, 56.05, 4778,3437, 34.32, 31.31, 31.30, 19.33, 17.40.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No, (9C) (cm'l) (1H, 13C, 191:) 1H NMR (500 MHz, CDC13) 8 12.12 (s, 1H), 798 (d, J: .2 Hz, 1H), 7.23 (dd, J : 8.3, 2.6 Hz, 5H), 7.13 (d,J= 7.9 Hz, 2H), 7.09 (d, .1: 79 Hz, 2H), 6.86 (d, .1 : 5.2 Hz, 1H), 5.80 (dq, J: 10.4, 6.1 Hz, 1H), 4.49 (p, J: 7.3 Hz, 1H), 3.98 (d, .1: 10.2 Hz, (Thin ?lm) HRMS-ESI (m/z) 1H), 3.93 (s, 3H), 2.82 (tp, J 3370, 2959, ([M+H]+) = 13.9, 6.9 Hz, 2H), 1.25 (d, 1734, 1649, .1: 6.1 Hz, 3H), 1.20 (d, J: calcd for 390 “r 1527, 1450, 69 Hz, 6H), 1.16 (d, J: 6.9 C H“ N 0 “ 31 9 9 1280, 1145, 5’ Hz, 6H), 0.86 (d, J = 7.2 Hz, 519.2853, found, 1045, 801, 3H).5 729 ‘519 2848' 13C NMR (126 MHz, CDC13)6171.75, 168.50, 155.32, 148.70, 147.36, 147.20, 140.41, 139.09, 138.58,130.51,127.91, , 126.50, 109.37, 7397,5739, 56.05, 47.80, 3364,3362, 23.98, 23.97, 23.93, 19.31, 17.45.
La) 4; La) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No, (0C) (cm'l) (1H, 13C, 191:) 1H NMR (500 MHz, CDC13) 8 12.12 (s, 1H), 8,36 (d, J: 7.9 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.07 4 6.89 (m, 6H), 6.86 (d, ,1: 5.3 Hz, 1H), 5.76 (dq, .1: 10.3, (11 Hz, 1H), 4.52 (p, J: 7.3 Hz, 1H), 3.94 (s, 3H), 3.91 (d, J (Thin ?lm) HRMS—ESI (m z) : 10.3 Hz, 1H), 2.17 (dd, .1: 3370, 2959, ([M+H]+) 20.2, 12.3 Hz, 12H), 1.24 (d, 1734, 1649, J: 6.1 Hz, 3H), 0.99 (d, J: 62116d for 391 1576, 1450, 7.2 Hz, 3H).
CZQHBSNZOE 1262’ ”47’ 491 2540 found 1050, 800, '491 21540 3 6"C NMR(126 MHz, 728 ‘ CDC13)6 171.72, 168.48, , 148.69, 140.38, 139.15, 138.98, 136.84, ,135.01,134.59, 130.50, 12993, 129.62, 129.33, 129.28, 125.27, 124.99, 109,35, 73.76, 57.12, 56.05, 47.88, 19.88, 19.79, 19.30, 924, 17.67. 1H NMR (400 MHz, CDC13) HRMS-ESI(I1zz) 5 11.51—1126(m, 1H), (Thin ?lm) ([M+H]+) 8.72 4 8.46 (m, 1H), 8.10 4 3358, 2936, 7.95 (m, 1H), 7.24 4 7.13 (m, 621166 for 392 1749, 1659, 4H), 7.03 4 6.82 (m, 5H), C25H77F ::~: 1508, 1223, 525 1413: ?guna 5.88 4 5.70 (m, 1H),5.314 1131 @5114“ 3 5.11 (m, 1244.04(m, 1H),4.014 3,93 (m, 3H), 1.32 —1.25(m,3H).
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (300 MHz, CDC13) 12.11 (d, 7:07 Hz, 1H), 8.34 (d, J: 8.0 Hz, 1H), 7.97 , (d, J: 5.3 Hz, 1H), 7.35 (dd, (Thin ?lm) #515535?” J: 8.5, 67 Hz, 1H), 7.25 — 3371, 2939, 7.08 (m, 1H), 6.86 (d, .1: 5.2 1734, 1649, calcd for Hz, 1H), 6.61 — 6.45 (m, 1599, 1500, F2N207, 4H), 5.89 (dq, J: 9.6, 6.1 1277, 1 150, 53 1 . 193 7, found, Hz, 1H), 4.83 (d, .1 : 9.7 Hz, 1034, 953 531.1926 1H), 4.71 — 4.44 (m, 1H), 3.94 (s, 3H), 3.83 (s, 3H), 3.73 (s, 3H), 1.23 (d, J: 6.2 Hz, 3H), 1.09 (d, J : 7.2 Hz, 1H NMR (400 MHz, CDC13) 512.09(s, 1H), 8.41 (d,J= 7.9 Hz, 1H), 7.98 (d, .1: 5.2 Hz, 1H), 7.32 _ 7.12 (m, 10H), 6.86 (d, J: 5.2 Hz, HRMS—ESI (m z) 111? if; (q’ i: :3 El * ([M+H]+) )7“ -» (p7,; ~ Z» 1H), 3.94 (s, 3H), 1.75 (s, calcd for 3H), 1.20 — 1.14 (m, 6H).
C26H29N2057 448.2071; found, 13C NMR (101 MHz, 449.2081. CDC13)6171.61, 168.58, 155.36, 148.74, 146.44, 144.98, 140.40, , 128.16, 128.10, 127.93, 127.35, 126.33, 126.16, 109.43, 7621,5606, 5040, 48.00, 23.98, 17.94, 15.94.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No, (CC) (cm'l) (H 13C, 191:) 1:1 mixture of reomers. 1H NMR (500 MHz, CDC13) 612.14(s, 1H), 12.09 (s, 1H), 8.34 (d, J: 8.0 Hz, . 1H), 8.24 (d, J: 79 Hz, $32)“ $91211) 1H), 8.00 (d, .1 : 5.2 Hz, 1734’ 1648’ HRMS-ESI (m/z) 1H), 7.98 (d, J = 5.2 Hz, ’ ’ ([M+H]+) 1H), 7.32 — 7.17 (m, 9H), 1575, 1527, , 7.1677.10(m,1H),6.88(d, , 1494, 1480, calcd for 395 J—5.2 Hz, 1H),6.86(d,J—_ _ 1450, 1279, C25H3-N205, .2 Hz, 1H), 5.88—5.75 (m, 1262, 1242, 435.1914, found,, , 1H)” 45644401" 1H)” 1144 1047 435 19243 909* 729 ’ ' 4,07 (d, J: 5.6 Hz, 1H), 4.05 7’02 ’ (d, J: 6.1 Hz, 1H), 3.95 (s, 3H), 3.94 (s, 1H), 1.29 (d, .1 : 7.2 Hz, 3H), 1.26 (d, J: 6.2 Hz, 3H), 1.24 (d, J = 6.2 Hz, 3H), 0.97 (d, .1: 7.2 Hz, 311). 1H NMR (400 MHz, CDC13) 11.96 (s, 1H), 8.24 (d, .1: 7.9 Hz, 1H), 7.98 (t, J: 54 (Thin ?lm) HRMSEEPSIIEm/Z) Hz, 1H), 7.63 — 7.59 (m, ([ ] ) 3372, 2985, 2H), 7.574 7.50 (m, 2H), 2228, 173 8, calcd for 7.40 — 7,37 (m, 2H), 7.37 — 1649, 1576, C27H25N405, 7.33 (m, 2H), 6.93 — 6.84 (m, 1529, 1504, 485.1819; found, 1H), 5.83 4 5.71 (m, 1H), 1452 4851824 4.617 4.46 (m, 1H), 4.21 (d, J: 9.3 Hz, 1H), 3.96 (s, 3H), 1.28 (d, .1: 6.] Hz, 3H), 1.13 (d, J: 7.2 Hz, 3H).
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No, (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8 12.01 (s, 1H), 8,31 (d, J: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.57 (d, J: 8.1 Hz, 2H), 7.52 (d, ,1: 8.: Hz, HRMS—ESI W Z) 2H), 7.42 (d, .14 8.3 Hz, (Thin ?lm) “MM“ 2H), 7.39 (d, J: 8.3 Hz, 2984 1739 397 16817 16177 calcd for 2H), 6.87 (d, J: 53 Hz, i“: 15771 15307 C27H25F(,N205, 1H), 5.90 i 5.82 (m, 1H), ' 1482 7 571.1662; found, 4.59 — 4.48 (m, 1H), 4.22 (d, 571.1671 J: 9.6 Hz, 1H), 3.94 (s, 3H), 1.29 (d, .1: 6.2 Hz, 3H), 1.03 (d, J : 7.2 Hz, 3H). 19F NMR (3 76 MHz, CDClg) 6 -6266, -6269. 1H NMR (400 MHz, CDCl;) 8 12.03 (s, 1H), 8.33 (d, .1: 8.0 Hz, 1H), 8.00 — 7.95 (m, 3H), 7.93 (d, J: 84 Hz, 2H)‘ 7'38 (d’ ‘1 : 8‘? HZ’ SI (m z) 2H)’ 7'35 (d’ J‘ 8‘3 HZ’ (Thin ?lm) +) 2H), 6.86 (d, J: 5.2 Hz, 3364 298] calcdfor lH),5.86 (dp,.]:9.l,7.1, h398 171316507 16077 15297 C31H35N209, 6.6 HZ, 1H), 4.60 — 4.50 (m, 1481’ 1418’ 579.2337, found, 1H), 4.35 (qd, J: 7.1, 2.8 1 579.2349 Hz, 4H), 4.22 (d, .1: 9.7 Hz, 1H), 3.93 (s, 3H), 1.37 (t, J: 7.2 Hz, 3H), 1.37 (t,J= 7.1 Hz, 3H), 1.28 (d, .1: 6.2 Hz, 3H), 1.05 (d, J: 7.2 Hz, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS N1VJR No, (‘0 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8 12.10 (s, 1H), 8.34 (d, J: 7.9 Hz, 1H), 7.90 (d, J: 5.2 Hz, 1H), 7.32 (d, J: 8.3 Hz, HRMS-ESI (m z) 1H), 7.09 (d, J: 87 Hz, (Thin ?lm) +) 1H), 0.80 (d, .1: 5.3 Hz, 3364, 2939, 1H), 0.85 — 0.80 (m, 3H), calcd for 1734, 1649, 0.74 (d, J: 2.0 Hz, 1H), 5.88 C27H29C12N2O7, 1488, 1449, (dq, .1: 9.0, 0.2 Hz, 1H), 563.1346, found, 1243 4.83 (d, J: 9.7 Hz, 1H), 4.54 563.13 54 (p, J: 7.2 Hz, 1H), 3.94 (s, 3H), 3.83 (s, 3H), 3.74 (s, 3H), 1.23 (d, J: 0.2 Hz, 3H),1.11(d,J= 7.2 Hz, 1H NMR (400 MHz, CDC13) 8 12.12 (s, 1H), 8.36 (d, J: 7.9 Hz, 1H), 7.90 (d, .1: 5.2 Hz, 1H), 7.32 (dd, J: 8.5, 0.8 Hz, 1H), 7.15 (dd,J= 9.0, 09 Hz, 1H), 0.85 (d, .1: SI(/1Iz) (Thin ?lm) 5.2 Hz, 1H), 0.02 — 0,39 (m, ([M+H]+) 3373, 2980, 4H), 5.99 — 5.89 (m, 1H), 1734, 1649, calcd for 4.82 (d, .1: 10.1 Hz, 1H), 1598, 1480, C29H33FZNZO77 4.55 (p, J: 7.2 Hz, 1H), 4.03 1263, 1161, 559.225; found, —3.81(m,7H),1.47(t,J= 1040 559.2258 7.0 Hz, 3H), 1.40 (1, .1: 7.0 Hz, 3H), 1.24 (01, J: 0.1 Hz, 3H), 1.10 (d,.]= 7.2 Hz, 1"’1: NMR (370 MHz, CDC13) —113.02, -11403.
[Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. :32; MP IR NMR No, (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 12.10 (s, 1H), 8,36 (d, .7: 7.9 Hz, 1H), 7.96 (d, J: 5.2 Hz, 1H), 7.29 (d, J: 8.3 Hz, 1H), 7.11 (d, .1: 82 Hz, . - HRMS-ESI (m z) 1H), 6.85 (d, .1: 5.3 Hz, g5“ $191310) ([M+H]+) 1H), 6.80 (dd, J: 82,20 ’ ’ Hz, 2H), 6.77 (d,J=2.0 Hz, 11:: 1?.35, 1650,4 calcd for 401 2 1;:1576, 4: 1H), 6.70 (d, .14 2.1 Hz, C29H33C12NZO7, , ), 5.92 (dq, .1— 102,62_ 1243,1147, 591.1659, found, HZ 1H) 482(d J=100 1041 591.1662 HZ, 1H), 4.62 2 4.47 (m, 1H), 4.03 4 3.81 (m, 7H), 1.47 (t, J: 6.9 Hz, 3H), 1.39 (t, .7: 6.9 Hz, 3H), 1.24 (d, .1 : 6.1 Hz, 3H), 1.12 (d,J: 7.2 Hz, 3H).
'H NMR (400 MHz, CDClg) 512.17(s, 1H), 8.40 (d, J: 7.9 Hz, 1H), 7.96 (d, J: 5.2 Hz, 1H), 7.28 (d, .1 : 7.8 Hz, 1H), 7.13 (d, J: 7.6 Hz, (Thin ?lm) HRMSEEPSIIfm/Z) 1H), 6.84 (d, J = 5.3 Hz, ([ 1 ) 3374, 2976, 1H), 6.70 4 6.50 (m, 4H), }: 1733, 1649, calcd for 5.96 (dq, J: 10.4, 6.1 Hz, 1527, 1450, C31H39N207, 1H), 4.90 (d, J: 10.2 Hz, 1261,1142, 551.2752; found, 1H), 4.53 (p, .1: 7.2 Hz, 1044 551.2716 1H), 4.05 4 3.80 (m, 7H), 2.26 (s, 3H), 2.22 (s, 3H), 1.47 (t, .1: 7.0 Hz, 3H), 1.39 (t, J: 6.9 Hz, 3H), 1.24 (d, J = 6.1 Hz, 3H), 1.04 (d, J: 7.2 Hz, 3H).
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR NIASS NO, (0C) (cm'l) (1H, 13C1 191:) 1H NMR (400 MHz, CDC13) 612.04(d,./: 0.7 Hz, 1H), 8.31 (d, J: 7.9 Hz, 1H), 7.97 (d, J: 5.2 Hz, 1H), 7.05 — HRMS-ESI(I112) 6.90 (m, 2H), 6.90 — 6.77 (m, ([M+H]+) 5H), 5.73 (dq, .1: 10.0, 0.1 Hz, 1H), 4.63 — 4.47 (m, 1H), calcd for 403 3.99 (d,J= 9.9 Hz, 1H), 3.94 C27H2‘JF2NZO7, (8,314), 3.86 (S, 3H), 3.85 (S,a ,, ’3 ,, 531.1944; found, 3H), 1.26 (d,J— 6.1Hz, 3H), 1.08 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) , -13751.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No. (0C) (cm'l) (1H, 13C. 191:) 1H NMR (400 MHz. CDC13) (s,1H),8.35(d,./: 8.0 Hz. 1H), 7.97 (d, J: 5.2 Hz, 1H). 7.20 (d, J: 8.6 Hz. 1H). 7.16 — 7.08 (m, 1H), 6.86 (d, .1: 5.3 Hz. 1H). 6.71 — 6.63 (m, 3H), 6.59 (d, J: 2.8 Hz, 1H), 5.65 (dq. J: 9.9, 6.1 Hz. 1H). 4.61 —4.46 (m, 1H), 4.39 (d, J: 10.0 Wilfg?ff/Z) Hz, 1H), 3.94 (s. 3H), 3.75 .2 (s. 3H), 3.72 (s, 3H). 2.37 (s. 404 : calcd for 3H), 2.30 (s, 3H). 130 (d, J ‘; C29H35N207, = 62 HZ, 3H), 1.09 (d, J: 523.2432; found, 7.2 Hz. 3H). 523.2426 (101MHz, CDC13)6171.7O, 168.56. 157.82, 157.67. 155.37, 148.74. 140.37. 137.93. 137.69.131.8813134, 130.50. . 128.13, 116.26. 116.08. 111.28, 110.86. 109.41, 75.02, 56.04. 55.08. 47.93. 46.22. 20.36, .30, 18.82. 17.78.
[Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No. (CC) (cm'l) (1H. 13C. 191:) 1H NMR (300 MHz. CDC13) 6 12.16 (s. 1H). 8.37 (d. J: 8.0 Hz. 1H). 7.97 (d. J: 5.2 Hz. 1H). 7.32 (d. J: 8.4 Hz.
. HRMS-ESI(7112) 1H). 7.11 (d. .1: 8.4 Hz.
SThm min) ([M+H]+) 1H). 6.85 (d. .1: 5.3 Hz. 3368. 2937. ’5 . 1H). 6.42 — 6.34 (m. 3H).a 2857. 1732. calcd for 405 6.32 (d. J— 2.5 Hz. 1H). 5.884 _ 1650. 1609. CZOHMNZOO. 1578. 1529. 555.2337.1ound.M . . (dq. .14 9.8.6.2 Hz. 1H). 4.82 (d.J—9.9 Hz. 1H). 4.61_ 1504 5552.27' 3 —4.46 (m. 1H). 3.94 (s. 3H). 3.82 (s. 3H). 3.75 (s. 3H). 3.74 (s. 3H). 3.73 (s, 3H). 1.23 (d. J: 6.2 Hz. 3H). 1.07 (d. .1: 7.2 Hz. 3H). 1H NMR (300 MHz. CDC13) 8 12.16 (d. .1: 0.6 Hz. 1H). 8.38 (d. .1: 8.0 Hz. 1H). 7.97 (d. J: 5.2 Hz. 1H). 7.30 (d. = 7.8 7. 0 = HRMS-ESI(I11Z) J8 l H Plfth37851d§d71L£ 7 (Thin ?lm) ([M4Hr) ‘ Z” )’ ‘ ( " . 5.3.0.6 Hz. 1H). 9 3373. 2936. calcd for (m. 5H). 6.57—6.53 (m.. 406 1734 1650 1 6‘1 1’ 1577’ C26H35NZO7. 1H). 5.92 (dq. .1: 9.9. 6.2 15291 1‘505’ 523.243 9. found. Hz. 1H). 4.90 (d. J 2 9.9 Hz. 1 523.2437 1H). 4.60 — 4.43 (m. 1H). 3.94 (s. 3H). 3.83 (s. 3H). 3.72 (s. 3H). 2.27 (s, 3H). 2.24 (s. 3H). 1.23 (d. J: 6.2 Hz. 3H). 1.03 (d. .1: 7.2 Hz.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (300 MHz, CDC13) 12.16 (d, J: 0.6 Hz, 1H), 8.38 (d, J: 7.9 Hz, 1H), 7.97 (d, J = 5.2 Hz, 1H), 7.20 (d, J: 2.2 Hz, 1H), 7.05 (d, J: HRMS—ESI (m z) 2.2 Hz, 1H), 6.98 4 6.84 (m, (Thin ?lm) ([M+H]+) 2H), 6.85 (dd, J = 5,4, 0.6 3370, 2937, Hz, 1H), 6.74 (d, J = 8.3 Hz, calcd for 407 2936, 1734, 1H), 6.64 (d, J: 8.3 Hz, (1)911ng?0 1650, 1576, 5235433101de 1H), 5.88 (dq, J: 102, 6.1 1528, 1501 523 21429 ’ Hz, 1H), 4.96 (d, J: 10.3 ‘ " Hz, 1H), 4.60 4 4.45 (m, 1H), 3.94 (s, 3H), 382 (s, 3H), 3.72 (s, 3H), 2.24 (s, 3H), 2.21 (s, 3H), 1.24 (d, J : 6.1 Hz, 3H), 1.02 (d, J: 7.2 Hz, 3H).
'H NMR (300 MHz, CDCH) for both diastereomers of a 1:1 e d12,14(d, J: 0.7 Hz, 1H), 12.07 (d, J: 0.6 Hz, 1H), 8,32 (d, J = 8.6 Hz, 1H), 8.29 (d, J: 8.4 Hz, 1H), 7.98 (d, J: 5.3 Hz, 1H), 7.97 (d, J: 52 Hz, . HRMS-ESI m/Z 1H), 7.20 4 7.11 (m, 2H), 91““ ?lm) ([M+H]+() ) 7.01 4 6.82 (m, 12H), 5.82 4 3368, 2940, ‘63 (m’ 2H)’ 5'04 (d’Ji, i 2839 1736 calcd for 408 1 7 10.1 Hz, 1H), 5.03 (d,J= 9.3 1650, 1577, C27H29F2N2O7, , 1528, 1478, 531.1937, found,, , Hz, 1H), 4.63 4 4.42 (m, 2H) 3 96 (S 3H) 3 95 (S 1453,1434 531.1942 7 " 7 7 3H), 3.93 (d,J= 2.1 Hz, 3H), 3.90 (d, J: 2.1 Hz, 3H), 3.78 (d, J: 1.8 Hz, 3H), 3.78 (d,J= 1.8 Hz, 3H), 1.37 (d,J= 7.2 Hz, 3H), 1.27 (d, J: 6.2 Hz, 3H), 1.26 (d, J = 62 Hz, 3H), 1.13 (d,J= 7.2 Hz, v) L11 L10 [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (300 MHz, CDC13) for the major isomer ofa 2:1 mixture ofdiastereomers d 12.09 (d, J: 0.6 Hz, 1H), 8.37 (d, J: 8.0 Hz, 1H), 7.98 . - HRMS'ESU’" Z) (d, .1: 5.2 Hz, 1H), 7.16 (dd, mm ?lm) ([Mm] ) J = 9.6 2.9 Hz 1H) 6.96 409 3?: 3:2 calcd for (dd, J: 913, 3.2 Hz, 1H), C27H29F2N207, 6.90 4 6.75 (m, 4H), 6.72 (d, 1 (30’ 1528’ 1495’ 1482’ 531.1937, found, J=4.7 Hz, 1H), 5.98—5.79 ’ 531.1937 (m, 1H), 4.91 —4.83 (m, 1H), 4.62 4 4.46 (m, 1H), 3.94 (s, 3H), 3.83 (s, 3H), 3.73 (s, 3H), 1.25 (d, J: 6.2 Hz, 3H), 1.11 (d, .1: 7.2 Hz, [Annotation] an None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR N01 (1H7 13c:1 19F) 1H NMR (300 MHz, CDC13) for 1:1 mixture of diastereomers 6 12.20 (s, 1H),12.11(s, 1H), 8.37 (d, J : 7.8 Hz, 2H), 7.97 (t, J: .2 Hz, 2H), 7.09 i 6.81 (m, 10H), 6.78 — 6.68 (m, 4H), .79 — 5,59 (m, 2H), 5.11 (dd, .1: 9.8, 6.2 Hz, 2H), 4.52 (dp, J: 10.0, 71 Hz, 2H), 3.95 (s, 3H), 3,94 (s, 3H), 3.89 (s, 3H), 3.86 (s, 3H), 3.84 (s, 3H), 383 (s, 3H), 3.81 (s, 3H), 3,79 (s, 3H), 3.73 (s, 3H), 3.70 (s, 3H), 1.35 (d, J: 7.2 Hz, HRMS-ESI (m/Z) 3H), 1.27 (d, J: 4.7 Hz, ([M+H]+) 3H), 1.25 (d, .1 : 47 Hz, 3H), 1.08 (d, J: 7.2 Hz, 3H calcd for C29H35N209, 13C NMR (126 MHz, 555.233 7; found, CDC13) for 1 :1 mixture of 555.23 17 diastereomers 5 171.68, 171.35, , , 155.31,155.29,152.81, , 152.74, 152.72, 148.71, 148.67, 147.33, 147.31, 147.15, 147.12, 140.36, 134.98, 13479, 134.67, 134.47, 130.57, 130.50, 123.69, 123.65, 123.62, 121.03, 120.94, 120.41, 120.24, 110.79, 110.57,]10.55,109.35, 109.33, 73.98, 60.39, 60.37, 60.27, 56.07, 56.05, 55.65, 5557,5555, 4792, 47.90, 41.96, 41.92, 18.80, 18.72, 1804, 17.74, [Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. n . :\§» \\\\\ ‘\‘\1 MP MASS NMR No, \'\'\x ‘ ~‘ (‘0 (1H7 13c:1 19F) 1H NMR (300 MHz, CDC13) for 1:1 mixture of diastereomers 8 12.20 (d, J : 0.5 Hz, 1H), 12.11 (d, J: 0.5 Hz, 1H), 836 (d, J: 7.8 Hz, 2H), 7.98 (dd, .1: 5.9, 5.2 Hz, 2H), 7132(ddd,J= 12.0, 72, 2.1 Hz, 2H), 7.17 — 7.09 (m, 2H), 7.09 4 6.80 (m, 10H), 5.76— 5.57 (m, 2H), 5108(t,J= 9.6 Hz, 2H), 4.59 4 4.41 (m, 2H), 3.96 (s, 3H), 3.94 (s, 3H), 3.83 (s, 3H), 3.79 (s, 3H), 3.69 (s, 3H), 3.68 (s, 3H), 2.36 4 2.19 (m, HRMS-ESI(/1Iz) 12H), 1.33 41,23 (m, 9H), ([M+H]+) 1.02 (d, J: 7.2 Hz, 3H). calcd for 411 [73C NMR (126 MHz, C29H35N2O7, CDC13) for 1:1 mixture of 523 .243 9; found, diastereomers 8 171.66, 523 .2409 171.15, 168.48, 168.46, 156.89, 156.80, 156.76, 155.32, 148.74, 148169, 140.38, 140.33, 133.98, 133.84, 133.74, , ,131.19,131102, 130.98, 130.56, 130.47, 130.09, 130.04, 129177, 129.74, , 126.71, 126.59, 126.34, 123.84, 123.80, , 109.36, 74.58, 74150, 60.29, 60.22, 60.19, 5608, 56.07, 47.89, 4785,4176, 41.70, 19.02, 18.93, 1803,1765, 16.69, 1666, 16.48, 1645.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No. (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) for 1:1 mixture of diastereomers 6 12.18 (s, 1H), 12.11 (s, 1H), 8.36 (d, J = 7.9 Hz, 1H), 8.28 (d, J: 7.7 Hz, 1H), 8.06 4 7.91 (m, 2H), 7.11 — 7.00 (m, 4H), 6.95 (t, J: 8.6 Hz, 2H), 6.89 4 6.82 (m, 4H), 6.70 (d, J 8.2 Hz, 2H), 6.65 (dd, J: 80,45 Hz, 2H), 5.70 (ddq, J : 12.3, 6.1, 3.3, 2.6 Hz, 2H), 4.62 (dd, J: 122,99 Hz, 2H), 4.49 (dp, J: 22.0, 7.2 Hz, 2H), 3.94 (s, 3H), 3.93 (s, 3H), 3.79 (s, 3H), 3.79 (s, 3H), 3.75 (s, 3H), 3.74 (s, 3H), 2.29 (s, 3H), 2.26 (s, 3H), 2.19 (s, 3H), 2.18 (s, 3H), 1.35 — 1.25 (m, 9H), 1.05 (d, J: 7.2 Hz, 3H). 13C NMR (101 MHz, CDC13) for 1:1 mixture of reomers 8 171.69, 171.27, 168.52, 157.74, 157.55, 155.32, 148.73, 140.69, 140.38, , 139.96, 130.52, 126.17, 126.11, 125.90, , 125.38, 120.47, 120.38, 119.87, 119.66, 109.38, 108.32, 74.97, 74.87, 56.03, 55.46, 55.43, 47.92, 47.89, 47.53, 18.74, 18.72, 17.98, 17.69,11.84,11.74, 11.42.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 812.03 (s, 1H), 8.28 (d, J: 8.0 Hz, 1H), 7.96 (d, J: 5.3 Hz, 1H), 7.05 (ddd, J = 8.4, .6, 2.2 Hz, 1H), 6.89 — 6.72 (m, 4H), 5.67 (dq, J: 9.6, 6.2 Hz, 1H), 4.86 (d, J = 9.6 Hz, 1H), 4.56 (dt, J: 8.1, 7.0 Hz, 1H), 3.97 (d, .1: 2.4 . Hz, 3H), 3.95 (s, 3H), 3.83 (Thm ?lm) 5 3374, 2941, HRMS—ESI(I112) (/dgé 2%z%)311{)2012615 3d; 1737, 1650, ([M4H]+) ' ‘ " 7 2’ HZ 73H) 1529, 1501, ‘ ’ ‘ calcd for 413 %:;?1 %:§T C27H27F4N207, 13C NMR (126 MHZ, 1263* 1243’ 567,1749,16und, CDC13) 5 , 168.61, 1058 952’ 567.1750 155.43, 148.73, 147.12(d,J 801 ’ : 7.3 Hz), 146.96 (d, .1: 7.6 Hz), 145.26 (d,J: 13.9 Hz), 143.28 (d,J= 13.8 Hz), 140.44, 130.25, 129.70, 129.47, 123.09 (dd, .1: 8.2, 3.8 Hz), 122.45 — 122.20 (111), 110.82 (d,J= 17.3 Hz), 110.57, 109.47, 72.53, 61.22 (d,J:4.1 Hz),61.16 (d, J: 3.6 Hz), 5611, 47.96, 42.46, 18.74, 17.75.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No. (0C) (cm'l) (1H.13C. 191:) 1H NMR (400 MHz. CDC13) 12.11 (s, 1H), 8.35 ((1.1: 8.0 Hz. 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.11 — 7.00 (m, 3H). 6.94 — 6.84 (m, 4H). .73 4 5.64 (m, 1H). 4.55 4 . 4.44 (m. 2H), 3.94 (s, 3H). $212)“ $1212 236 (s, 3H), 2.28 (s, 3H). 1735’ 1550’ HRMS—ESI+(mz) 2.25 (s. 6H), 1.30 (d, .1: 5.1 1576’ 1528’ ([M+H] ) Hz, 3H). 1.03 (d, J = 7.2 Hz. 1 1 3H). 1501,1481, calcd for 1451, 1336, C29H35NZos, 13C NMR (126 MHZ, 1280. 1263, 491.2540. found, CDC13)5171.84, 168.52. 1212 1145 4912536 1045 801’ 155.34. 148.73, 140.40, 733 ’ . 138.45. 135.47, , 133.53, 133.33, 130.60, 130.49, 130.27, 128.60, 127.81. 127.27, 126.95, 109.39, 75.10, 56.07, 47.89, 47.34, 21.29, 21.22, 19.79, 19.75, 18.78, 17.66.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 6 12.11 (s, 1H), 8.35 ((1.1: 8.0 Hz, 1H), 7.97 (d, J: 5.2 Hz, 1H), 7.18 (d, J: 7.9 Hz, 1H), 7.12 (d, J: 7.7 Hz, 1H), 6.98 4 6.89 (m, 3H), 6.87 — 6.81 (m, 2H), 5.69 (dq,J= 100,62 Hz, 1H), . - 45844.48 (m, 1H), 4.45 (d, $2119“ $191317) J = 10.0 Hz, 1H), 3.94 (s, 1734’ 1649’ HRMSESIfm/z) 3H), 2.35 (s, 3H), 2.29 (s, ([M+H] ) 3H), 2.25 (s, 3H), 2.21 (s, _, 1576‘ 1527’ 1 ‘ 1 3H), 1.30 (d, J: 6.2 Hz, 1500, 1480, calcd for 415 3H) 105 (d J: 7 2Hz 7 ' ‘ a { 1450, 1329, C29H35N205, "51%)' 1280, 1202, 491.2540, found, 1242,1159, 491.2536 13CNMR(126MHZ’ 1043, 908, CDC13)5171.71, 168.51, 799, 728 155.32, , 140.38, 136.43, 136.33, 136.15, 135.95, 135.90, 135.58, 131.50, 131.15, 130.49, , 127.05, 126.85, 126.58, 109.37, 75.04, 56.06, 47.89, 46.81, 20.84, .80, 20.12, 20.07, 18.85, 17.71. ation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8 12.05 (s, 1H), 8,36 (d, J: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.12 (dd, J: 8.4, 6.0 Hz, 1H), 7.06 — 7.00 (m, 2H), 6.93 4 6.77 (m, 4H), .60 (dq, J: 9.6, 6.2 Hz, 1H), 4.61 — 4.50(m,1H), 4.48 (d, .1: 9.6 Hz, 1H), 3.94 . (s, 3H), 2.35 (s, 3H), 2.28 (s, $213)“ $1311; 3H), 1.34 (d, J = 6.2 Hz, 3H)” 1'10 £111] 7‘2 HZ’ 1736, 1649, HRMS—ESI (m z) 1576, 1528, ([M+H]+) 3 )‘ 32:” $132 calcd for 13C NMR (126 MHz, 1279’ 1263’ C27H29F2N205, CDC13) 8 171.60, 168.60, 1240’ 1184’ 499.2039, found, 161.36 (d, J: 244.0 Hz), 11457 1044’ 499.2035 155.35, 148.72, 140.57 (d, .1 9101803 ’ : 6.5 Hz), [4048, 139.99 7’28 7 (d, J: 6.6 Hz), 132.34 (01, J = 3.2 Hz), 132.07 (d, J: 7.8 Hz), 132.00 (d, .1: 3.3 Hz), 131.72 (d,J= 7.9 Hz), 130.39, 114.85 (d,J=22.3 Hz), 11432 (d, .1: 22.3 Hz), 113.72 (d,J: 20.7 Hz), 113.42 (d,J= 20.5 Hz), 109.44, 74.21, 56.08, 47.79, 47.70, 19.41, 19.36, 18.76, 17.68.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. \\ MP IR NMR No. (0C) (cm'l) (1H. 13C. 191:) 1H NMR (400 MHz. CDC13) 512.07(s. 1H). 8.34 (d. J: 8.0 Hz. 1H). 7.98 (d. J: 5.2 Hz. 1H). 7.01 — 6.90 (m. 2H). 6.88 — 6.80 (m. 3H). 6.71 (ddd. J: 8.9. 3.9. 3.1 Hz, 1H). 6.64 (ddd. J = 8.9. 3.9. 3.1 Hz. 1H). 5.85 (dq, J : 12.2.6.1 Hz. 1H). 4.70 (d.
J: 10.4 Hz. 1H). 4.61 — 4.52 (Thin ?lm) (m. 1H). 3.94 (s. 3H). 3.74 3367. 2940. HRMS—ESI (m z) (s. 6H). 1.31 (d. .1: 6.1 Hz. 1738. 1650. ([M+H]+) 3H). 1.11 (d. J: 712 Hz. 1530. 1498. 3H). calcd for :2“: 1482’ 1453’ C7 H7IF7N7O I“ ::~: 1281. 1264. 3177 £6111; "C NMR (126 MHz. 1242.1210. ‘531 11931 ’ CDC13)6171.53. 168.53. 1149. 1037. ' 155.99 (d. J: 24.2 Hz). 802. 730 155,76 4 155.59 (m). 155.32. 154.09 (d,J= 24.6 Hz). 148.70. 140.40. 130.42. 127.85 (d. .1: 15.9 Hz). 127.56 (d,J= 16.3 Hz). 116.26 (d,J= 24.9 Hz). 115.93 (d../: 24.8 Hz). 115.16. 114.19. 11304 (d.J = 8.2 Hz). 109.39. 72.25. 56.07. 55.69. 47.85. 43.42. 1894. 17.72.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 512.09(s, 1H), 8,34 (d, J: 8.0 Hz, 1H), 7.97 (d, J: 5.2 Hz, 1H), 7.27 (t, J: 8.6 Hz, 1H), 7.16 (t,J= 85 Hz, 1H), 6.86 (d, .1: 5.2 Hz, 1H), 6.64 — 6.54 (m, 3H), 6.47 (dd, J: 12.1, 2.6 Hz, 1H), 5.79 (dq, J : 12.0, 6.1 Hz, 1H), 4.66 4 4.52 (m, 2H), 3.94 (s, 3H), (Thin ?lm) 3.75 (s, 3H), 3.72 (s, 3H), 3369, 2938, 1.28 (d, .1: 6.1 Hz, 3H), 1.14 162: i233: (d’ J 7‘2 HZ’ DH) HRMS-ESI+(m/z) ([M+H] ) 1529, 1507, 13C NMR (126 MHz, 1481, 1443, calcd for CDC13) 5 171.55, , 1320, 1282, C27H26FZNZO7, 161.19 (d, J: 245.6 Hz), 1264, 1242, 531.1937, found, 161.00 (d, J: 2458 Hz), 1195,1154, 531.1933 159.75 (d,J: 11.3 Hz), 1031, 951, 159.47 (d,J= 11.3 Hz), 849, 834, 155.35, 148.69, 140.39, 800, 731 130.42, 129.87 (d, .1: 6.2 Hz), 129.23 (d,J= 5.9 Hz), 119.53 (d,J= 14.6 Hz), 119.33 (d,./: 15.0 Hz), 110.16(d,J=3.0Hz), 109.66 .0 Hz), 109.38, 101.82 (d,./’:26.7 Hz), 101.59 (d, J: 26.6 Hz), 72.49, 56.05, 55.48 (d,J= 6.8 Hz), 47.90, 41.70, 18.91, 17.79. v) 0 La) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) (s, 1H), 8,34 (d, J: 8.0 Hz, 1H), 7.97 (d, J: 5.2 Hz, 1H), 7.54 (d, J: 7.8 Hz, 1H), 7.30 (d, J: 8.0 Hz, 1H), 7.12 (dd, .1: 7.9, 1.6 Hz, 2H), 7.04 (d, J: 1.8 Hz, 1H), 6.98 (d, J: 1.7 Hz, $25“ $191211). - 1H), 6.86 (d, .1: 5.2 Hz, 1H), 5.99 (dq, J: 9.5, 6.2 1737’ 1651’ HRMS-ESI (7112) Hz, 1H), 5.00 (d, J: 9.4 Hz, 1616: 1577: ([M+H]+) 1H), 4.5:) 4 4.548 (m, 1H), "94 (Pm 3‘89 (5’ :H)’ 1529, 1454, calcd for 419 3.81 , (s, 3H), 1.26 (d,J— 6.2 1;, 14171 1326, C29H29F6N207, HZ 3H) 1 05 (d 1: ,7 2H2 1241,1119, 631.1873,f0und, 7‘ 1 ‘;H)“ ‘ 1 1080, 1032, 631.1876 ' 905, 860, 13 CNMR(126MHz, 801,738 CDC13)5171,62, 168.58, 157.53, 155.38, , 140.44, 132.32 ((1, J: 8.6 Hz), 130.37, 130.18, 130.04, 129.47, 125.02, 122.83, 117.30, 116.98, , 10783410697 (m), 72.18, 56.07, 55.75, 55.69, 47.82, 18.89, 17.66.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (500 MHz, CDC13) 12.04 (d, J: 0.6 Hz, 1H), 8.34 (d, J: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 6.86 (d, .1: 5.2 Hz,1H),6,65 4 6.52 (Thin ?lm) HRMla‘EESIU’" Z) (m, 4H), 6.45 (ddt, J: 24.3, (1 1 ) 3369, 2940, 10.5, 2.2 Hz, 2H), 5.69 (dq, J 1737, 1592, calcd for = 10.1, 6.1 Hz, 1H),4,61— 1453, 1135, C27H26F2N207, 4.50 (m, 1H), 3.97 4 3.91 (m, 1057, 849, 3 7, found, 4H), 3.77 (s, 3H), 3.75 (s, 730 531.1924 3H), 1.29 4 1.24 (m, 3H), 1.11 (d, .7: 7.2 Hz, 3H). 191: NMR (471 MHz, CDC13) 4110.48 4 —110.65 (m), _ 11108 (t, J: 10.0 Hz), 1H NMR (500 MHz, CDCl;) 512,10(s, 1H), 8.35 (d, .1: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 6.86 (d, J: 5.2 Hz, 1H), 6.46 4 6.43 (m, 4H), 6.27 (dt, J: 26.6, 2.2 Hz, 2H), 5.75 (dq, J: 10.3, 6.1 Hz, 1H), 4.58 4 4.47 (m, (Thin ?lm) #:4513155" Z) 1H), 3.94 (s, 3H), 3.89 (d, J 3371, 2938, = 10.5 Hz, 1H), 3.76 (s, 6H), 1735, 1593, calcd for 3.74 (s, 6H), 1.30 4 1.23 (m, 1454, 1204, C29H35N209, 3H), 1.05 (d, J : 7.2 Hz, 1150, 1063, 555.2337, found, 3H). 730 555.2329 13C NMR (126 MHz, CDC13)6171.70, 168.53, 160.93, 160.75, 155.32, ,143.38,143.10, 140.39, 130.45, 109.36, 106.42, 106.08, 98.42, 98.3 5, 7311,5822, 5606, 55.30, 55.26,47.87,19.21, 17.70.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (500 MHz, CDC13) 8 12.11 (s, 1H), 8.36 (d, J: 8.0 Hz, 1H), 7.98 (d, .1: 5.2 Hz, 1H), 6.86 (d, J = 5.2 Hz, 1H), 6.69 (dd, .1: 38,18 Hz, 2H), 6.64 (t, .1 : 1.9 Hz, 2H), 6.55 (t, J: 2.0 Hz, 1H), 6.49 (t, J: 1.9 Hz, 1H), 5.75 (dq, .1: 10.5, 6.2 Hz, 1H), 4.58 — 4.48 (m, 1H), 3.94 (s, . HRMS-ESI (I112) 3H), 3.89 (d, J = 10.5 Hz, ghm min) ([M+H]+) 1H), 3.76 (s, 3H), 3.73 (s, 1,; 5372, 29.) 7, 5 q :5 1735, 1594,, 3H), 2.29 (s, 5H), 225 (s, calcd for 422 3H), 1.25 (d, J — 6.2 Hz,_ ,6, 1528, 1452, C29H35N207, ",H) 1 00 (d 1 151, 1065, 523.2439; found, 1 ' I: 7 H) ‘ 1 HZ’ 730 523.2434 ' 13C NMR (126 MHz, 6171,74, 168.51, 159.74, 159.61, 155.32, 148.70, 142.68, 142.37, 140.40, 139.79, 139.36, 130.47, 121.27, 121.12, ,112.61,111.34, 110.82, 109.36, 73.43, 57.89, 5606,5515, 55.11, 47.86, 21.69,21.61,19.25, 17.66.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No, (cm ) (1H7 13c:1 19F) 1H NMR (500 MHz, CDC13) 8 12.10 (s, 1H), 8.33 (d, .7: 8.0 Hz, 1H), 7.97 (d, ,1: 5.2 Hz, 1H), 7.02 (dd, J: 7.5, 0.9 Hz, 1H), 6.97 (dd, J: SI (/77 Z) 7.6, 0.8 Hz, 1H), 6.86 (d, .1: (Thin ?lm) ([M+H]+) 5.2 Hz, 1H), 6.80 (dt,J= 3370, 2937, 7.5, 2.1 Hz, 2H), 6.74 (d,J= 1734, 1649, calcd for 1.6 Hz, 1H), 6.71 (d, .1: 1.6 1528, 1452, C29H35NZO77 Hz, 1H), 5180(dq,J= 10.3, 1260, 1137, 523 .243 9, found, 6.1 Hz, 1H), 4.58 — 4.47 (m, 1039, 729 523 .2434 1H), 3.96 (d, .7: 10.3 Hz, 1H), 3.94 (s, 3H), 3.80 (s, 3H), 3.78 (s, 3H), 2.14 (s, 3H), 2.11 (s, 3H), 1.27 (d, .1 : 6.1 Hz, 3H), 1.00 (d,J: 7.2 Hz, 3H). lH NMR (500 MHz, CDC13) 512.05(s, 1H), 8.33 (d,J= 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.01 4 6.91 (m, 4H), 6.91— 6.79 (m, 3H), HRMS-ESI (m ”2) 5.65 (dq, J: 9.6, 6.2 Hz, (Thin ?lm) ([M+H]+) lH),4.6144.51(m, 1H), 3370, 2938, 3,94 (s, 3H), 3.92 (d, J: 9.7 calcd for 424 1736, 1515, Hz, 1H), 3.85 (s, 3H), 3.83 C27H29F2N2O77 1442, 1275, (s, 3H), 1.24 (d, .1: 6.1 Hz, 531.1937, found, 1216, 731 3H), 1.13 (d,J: 72 Hz, ”P NMR (471 MHz, CDC13) -134.12(dd,J= 12.1, 8.5 Hz), —134,58 (dd, J: 12.1, 8.7 Hz).
[Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (500 MHz, CDC13) 12.13 (d, .7: 0.6 Hz, 1H), 8.36 (d, J: 8.1 Hz, 1H), 7.98 (d,J= 5.1 Hz, 1H), 7.06 (ddd, .1: 9.0, 7.1, 2.4 Hz, mm ?lm). - HRMS-ESI (m z) 2H), 7.01 (d, .1: 2.0 Hz, ([M+H]+) 2H), 6.86 (d, J: 5.2 Hz, 3370, 2941, , 1H), 6.72 (d, .1— 8.4 Hz, 1734, 1649, calcd for 425 1H), 6.68 (d, .14 8.4 Hz,, 1503, 1243,, , C29H35NZO7, , , , 1H),5.71(dq,J— 101,61 1135,1033, 52324321611116, HZ 1H) 4 58 _ 4 48(m3 801, 729 523.2428 1 3 ' ' 1H), 3.94 (s, 3H), 3.88 (d, .1 : 10.1 Hz, 1H), 3.77 (s, 3H), 3.74 (s, 3H), 2.16 (s, 3H), 2.12 (s, 3H), 1.24 (d, .1: 6.2 Hz, 3H), 1.03 (d, J: 7.1 Hz, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No, (1H7 13c:1 19F) 1H NMR (500 MHz, CDC13) 12.14 (s, 1H), 8,38 (d, J: 8.0 Hz, 1H), 7.97 (d, J: 5.2 Hz, 1H), 7.05 (d, J: 3.0 Hz, 1H), 6.88 (d, ,1: 3.1 Hz, 1H), 6.85 (d, .1: 5.2 Hz, 1H), 6.77 (d, J: 8.9 Hz, 1H), 6.72 — 6.55 (m, 3H), .94 (dq, .1: 10.1, 6.1 Hz, 1H), 4.93 (d, J: 10.1 Hz, HRMS-ESI (m/Z) (Thin ?lm) 1H), 4.60 — 4.49 (m, 1H), ([M+H]+) 3372, 2940, 3.94 (s, 3H), 3.82 (s, 3H), 1735, 1650, calcd for 3.74 (s, 3H), 3.71 (s, 6H), 1498, 1223, C29H35N209, 1.28 — 1.22 (m, 3H), 1.04 (d, 1047, 804, 555.2337; found, .1: 7.2 Hz, 3H). 730 04 13CN1\4R(1261V1Hz, CDC13)6 171.72, 168.47, 155.28, , 153.37, 151.78,151.70,148.67, 140.35,130.55,130.51, 116.43, 115.36, 112.05, 112.00,111.68,111.46, 109.31, 627, 56.05, 55.62, 5557,4790, 18.87, 17.81.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (500 MHz, CDC13) 12.10 (s, 1H), 8.36 (d, J: 8.0 Hz, 1H), 7.97 (d, J: 5.2 Hz, 1H), 7.06 (d, J: 8.4 Hz, 1H), 6.95 (d, ,1: 8.4 Hz, 1H), 6.90 (d, .1: 2.7 Hz, (Thin ?lm) “11131551,? Z) 1H), 6.86 (d, J: 5.2 Hz, 3370, 2939, 1H), 6.82 (d, J: 2.7 Hz, 1736, 1529, calcd for 1H), 6.66 (dd, .1: 8.4, 2.7 1452, 1243, C29H35N207, HZ, 1H), 6.60 (dd, J: 8.3, 1143, 1043, 523.2439, found, 2.7 Hz, 1H), 5.67 (dq, J: 801, 730 523.2420 10.0, 6.2 Hz, 1H), 4.58 4 4.49 (m, 1H), 4.46 (d, J: .1 Hz, 1H), 3.94 (s, 3H), 3.74 (s, 3H), 3.73 (s, 3H), 2,34 (s, 3H), 2.26 (s, 3H), 1.32 (d, J: 6.2 Hz, 3H), 1.05 (d, .1: 7.2 Hz, 3H). 1H NMR (400 MHz, CDC13) (s, 1H), 8.32 (d, J: 7.9 Hz, 1H), 7.98 (d, .1: 5.2 Hz, 1H), 7.43 (dd, J: 8.7, .6 Hz, 1H), 7.23 (dd, J: 8.7, 5.6 Hz, 1H), 7,1 1 (dd, .1 : 9.6, 2.8 Hz, 1H), 7.04 (dd, (Thin ?lm) #5151315?” J= 9.6, 2.8 Hz, 1H). 6.96 _ 3368, 2933, 6.89 (m, 2H), 6.87 (d, .1: 5.2 1736, 1648, calcd for Hz, 1H), 5.63 (dq, J: 8.7, 1528, 1492, C29H33F2N207, 6.2 Hz, 1H), 4.71 (d, J: 8.8 1481, 1263, 560.2283, found, Hz, 1H), 4.63 (d, .1: 12.4 1094 560.2285 Hz, 1H), 4.58 4 4.36 (m, 4H), 3.94 (s, 3H), 3.43 (s, 3H), 3.38 (s, 3H), 1.30 (d, .1 : 6.2 Hz, 3H), 1.12 (d, .1: 7.2 Hz, 3H).
”P NMR (376 MHz, CDClg) —115,46, -115,76.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 812.06(s, 1H), 8,33 (d, J: 7.9 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.45 (dd, J: 8.7, .6 Hz, 1H), 7.21 (dd, J: 8.7, 5.6 Hz, 1H), 7. 12 (dd, .1 = 9.6, 2.8 Hz, 1H), 7.07 (dd, . HRMSESW" Z) mm ?lm) ([M+H] ) J= 9.7, 2.8 Hz, 1H), 6.94 4 429 1’ .26: 12:71; calcd for 6.84 (m, 3H), 5.73 4 5.56 (m, 1537’ 1481’ C31H37F2N207, 1H), 4.78 4 4.63 (m, 2H), 1262’ 109,; 587.2563, found, 460 4 4.38 (m, 4H), 3.94 (s, ‘ ‘ 587.2559 3H), 3.62 4 3.42 (m, 4H), 1.33 4 1.25 (m, 6H), 123(1, J: 7.0 Hz, 3H), 1.12 (d, J: 7.2 Hz, 3H). 19F NMR (376 MHz, CDC13) 8 4115.57, 41585. 1H NMR (400 MHz, CDC13) (s,1H),8,35(d,J= 8.0 Hz, 1H), 7.97 (d, .1: 5.3 Hz, 1H), 7.48 4 7.07 (m, 6H), HRMSEEPSIIfm/Z) 6.85 (d, J = 5.3 Hz, 1H), 6.58 ([ 1 ) (1,7: 8.3 Hz, 2H), 5.85 (dd, calcd for J: 10.1, 6.0 Hz, 1H), 4.72 - C26H23FN206, 4.38 (m, 2H), 3.93 (S, 3H), 483.1931; found, 3.83 (s, 3H), 1.25 (d, J: 6.2 483.1928 Hz, 3H), 0.99 (d, J : 7.2 Hz, ”P NMR (3 76 MHz, CDC13) 4113.13.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan CmNE,d. MP 1R NMR (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 512.09(s, 1H), 8.33 (d, J: 7.9 Hz, 1H), 7.97 (d, J: 5,2 55???), Hz, 1H), 7.36 — 7.07 (m, 6H), 6.94 — 6,78 (m, 3H), 5.78 (dq, J: 10.4, 6.1 Hz, 1H), calcd for 4.52 (p, J: 7.3 Hz, 1H), 4.29 ngHngN205, (d, J: 103 HZ, 1H), 393 (S, 467.1982; found, 3H), 2.39 (s, 3H), 1.28 (d, J 467.1976 = 6.1 Hz, 3H), 1.00 (d, J = 7.2 Hz, 3H).
”P NMR (3 76 MHz, CDC13) -116.60. 1H NMR (400 MHz, CDC13) 512.09(s, 1H), 8.34 (d, J: 8.0 Hz, 1H), 7.97 (d, .1: 5.2 Hz, 1H), 7.47 — 7.20 (m, 5H), 7.20 — 7.10 (m, 1H), 6.86 (d, ??”, J= 5.2 Hz, 1H), 6.57 (td, J = 8.3, 2.6 Hz, 1H), 6.49 (dd, J calcd for = 10.9, 2.5 Hz, 1H), 5.83 C26H23FN206, (dq, J: 10.2, 6.1 HZ, 1H), 483.1931; found, 4.61 — 4.49 (m, 2H), 3.94 (8, 483.1931 3H), 3.76 (s, 3H), 1124 (d, J = 6.1 Hz, 3H), 1.07 (d,J= 7.2 Hz, 3H). 19F NMR (376 MHz, CDC13) -11349.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 512.07(s, 1H), 8.34 (d, J: 8.0 Hz, 1H), 7.97 (d, .1: 5.2 Hz, 1H), 7.35 (dd, J: 8.7, .7 Hz, 1H), 7.31 — 7.13 (m, HRMS-ESI(/11z) 5H), 6.92 — 6.80 (m, 2H), ([M+H]+) 6.76 (dd, J = 9.7, 28 Hz, 1H), 5.75 (dq, J: 10.1, 6.1 C 3163;]?— Hz, 1H), 4.53 (p, .1: 7.3 Hz, 92882, féu?d 1H), 4.26 (d, J: 10.1 Hz, ‘467 11974 * 1H), 3.93 (s, 3H), 2.30 (s, ' 3H), 1.26 (d, .1: 6.1 Hz, 3H), 1.05 (d, J: 7.2 Hz, ”P NMR (3 76 MHz, CDC13) -116.99. lH NMR (400 MHz, CDCl;) 12.12 (s, 1H), 8.35 (d,J= 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7. 19 (d, .1 : 8.0 Hz, 2H), 7.17 — 7.08 (m, 1H), #1315535?” 7.01 (d, J = 8.0 Hz, 2H), 6.86 (d, .1: 5.2 Hz, 1H), 6.64 — calcd for 6.51 (m, 2H), 5.82 (dq, J: C27H30FN2O6, 9.9, 6.2 Hz, 1H), 4.63 — 4.41 497.2088; found, (m, 2H), 3.94 (s, 3H), 3.83 497.2077 (8, 3H), 2.25 (s, 3H), 1.24 (d, J: 6.2 Hz, 3H), 1.03 (d,J= 7.2 Hz, 3H), 1"’1: NMR (376 MHz, CDC13) —113.3 _ v) \1 La) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR “AASS Nb. 6C) (mn4) CH 13) ?iymy?k(40034Hz.cx)Ch) 812l1(g1}D,834(d“/: 80HL1HL7%M¢J:52 ItJHy7w—7?mmJH) 113mw?=81H12H)700 HRz??f?g"? @??:80HL2H)695— 680(nL3PD,576(dq”/= calcd for 10.2, 6.2 Hz, 1H). 4.53 (p, J C27H30FN205, : 7.3 HZ, 1H), 4.25 (d, .l: 48L21391bund, 10211;]fD,393(&3}D, 4812133 238(g3fD,224(&3}D. 127m??:61H;3H)104 (dJ:?2HL3H) 76w?k,CDCh) —H68O ?JNm?{m00NHh;CDCh) SQJOQJHLSyde: 80H11H1797QLJ=52 HL]H)7I%7220m1HL m2H;7mm¢ 2HL685QLJ= Wilfg?ff/Z) 5.2 Hz. 1H). 6.56 (td, J = 83,26P?,“?.648?m?l calcd for : 10.9. 2.5 Hz. 1H), 5.80 C27H30FN206, (dq, J: 10.4, 6.1 HZ, 1H), 497208&1bun¢ 462—z¥44(nL2PD,394(& zw7mns 3H)3??g3H)228@ 3H)LB(¢J=61HL 3nymu¢1:72H; wa??KG76NH?,CDCh) 6—H369 [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 812.07(s, 1H), 8,33 (d, .7: 8.0 Hz, 1H), 7.97 (d, J: 5.2 Hz, 1H), 7.33 (dd, J: 8.7, .8 Hz, 1H), 7.18 _ 7.00 (m, HRMS-ESI(/11z) 4H), 6.94 — 6.81 (m, 2H), ([M+H]+) 6.74 (dd, J = 9.7, 2.8 Hz, 1H), 5.73 (dq, J: 10.1, 6.1 C 61211163131066— Hz, 1H), 4.52 (p, .1: 7.3 Hz, 1315, féudd 1H), 4.22 (d, J: 10.3 Hz, ‘48] 2’12] 3 1H), 3.94 (s, 3H), 2.29 (s, ' 3H), 2.28 (s, 3H), 1.25 (d, .1 : 6.1 Hz, 3H), 1.04 (d, J: 7.2 Hz, 3H).
"’F NMR (3 76 MHz, CDC13) 8 —117.22. lH NMR (400 MHz, CDClg) 512.09(s, 1H), 8.33 (d,J= 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.31 _ 7.23 (m, 2H), HRMS-ESI (m/z) 7.12 (dd, J = 8.2, 6.5 Hz, ([M+H]+) 1H), 6.94 — 6.80 (m, 3H), 6.64 _ 6.52 (m, 2H), 5.81 calcd for 438 (dq, J : 10.0, 6.2 Hz, 1H), 501618377f6undH2_F7N706 4.61 — 4.38 (m, 2H), 3.94 (s, ‘501 1829 ° 3H), 3.83 (s, 3H), 1.25 (d, .1 : 6.2 Hz, 3H), 1.06 (d, J: 7.2 Hz, 3H).
”P NMR (3 76 MHz, CDC13) 8 -112.82, -116.36. ation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 512.08(s, 1H), 8.33 (d, J: 7.9 Hz, 1H), 7.970111: 52 Hz, 1H), 7.33 — 7.12 (m, 3H), migfglfm‘) 6.97 — 6,83 (m, 5H), 5.73 ([ 1 ) (dq, .1: 9.9, 6.1 Hz, 1H), calcd for 4.68 — 4.46 (m, 1H), 4.28 (d, C26H2-F2N205, J: 10.1 Hz, 1H), 3.94 (3, 485.1888; found, 3H), 2.36 (s, 3H), 1.28 (d, .1 485.1874 = 6.1 Hz, 3H), 1.09 (d, J: 7.2 Hz, 3H).
”P NMR (3 76 MHz, CDC13) —115.88, -116.28. 1H NMR (400 MHz, CDC13) 512.08(s, 1H), 8.33 (d,J= 8.0 Hz, 1H), 7.97 (d, .1: 5.2 Hz, 1H), 7.30 _ 7.19 (m, 3H), 6.99 — 6.90 (m, 2H), 6.86 (d, Wiggly/z)7 J: 5.3 Hz, 1H), 6.57 (td, J= ([ 1 ) 8.3, 2.5 Hz, 1H), 6.50 (dd, .1 calcd for = 10.9, 2.5 Hz, 1H), 5.92 C26H2‘F2N2O6, 5.68 (m, 1H), 4.64 — 4.40 (m, 501.1837; found, 2H), 3.94 (s, 3H), 3.76 (s, 501. 1824 3H), 1.23 (d, J : 6.2 Hz, 3H), 1.09 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) -11315, -11603.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 812.06(s, 1H), 8,34 (d, J: 8.0 Hz, 1H), 7% (d, J: 5.2 Hz, 1H), 7.33 (dd, J: 8.7, .7 Hz, 1H), 7.19 (dd, J: 8.5, 5.4 Hz, 2H), 7.02 4 6.90 W151i??? Z) (m, 2H), 6.91 — 6.82 (m, 2H), 6.77 (dd, J: 9.7, 2.8 Hz, calcd for 1H), 5.71 (dq, J: 9.8, 6.1 C26H27F2N205, HZ, 1H), 4.53 (p, J = 7.3 HZ, 485.1888; found, 1H), 4.26 (d, J: 9.9 Hz, 485.1876 1H), 3.93 (s, 3H), 2.27 (s, 3H), 1.25 (d, J : 6.2 Hz, 3H), 1.07 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) 8 41541—11665. 1H NMR (400 MHz, CDC13) (s,1H),8,35(d,J= 8.0 Hz, 1H), 7.98 (d, .1: 5.2 Hz, 1H), 7.20 4 7.13 (m, HRMSfESIXm/Z) 1H), 7.12 4 7.06 (m, 5H), ,(Thm ?lm). ([NHH] ) 7.03 4 6.97 (m, 1H), 6.96 4 calcd for 442 3:2 12:3 6.92 (m, 1H), 6.85 (d, J : 5.2 15767 1529, C27H31N205, HZ, 1H), 579 (dq, J=103, 148 1” [452’ 463.2224; found, 6.1 Hz, 1H), 4.57 4 4.44 (m, 1 ‘ 463.2227 1H), 3.97 (d, J : 10.4 Hz, 1H), 3.93 (s, 3H), 2.31 (s, 3H), 2,27 (s, 3H), 1.25 (d, .1 : 6.1 Hz, 3H), 0.97 (d, J: 7.2 Hz, 3H).
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR NO, (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8 12.09 (s, 1H), 8,35 (d, .7: 7.7 Hz, 1H), 7.97 (d, .1: 5.2 Hz, 1H), 7.23 (dd, J: 8.5, 6.6 Hz, 1H), 7.17 (dd, J: 8.6, 5.8 Hz, 1H), 6.90 4 6.73 W151i??? Z) (m, 2H), 6.57 (td, J: 8.3, 2.5 Hz, 1H), 6.49 (dd, J: 10.8, \ calcd for 2.5 Hz, 1H), 5.70 (dq, J: : C27H29F2N206, 10.1, 6.1 HZ, 2H), 4.75 (d, J 21, found, = 10.2 Hz, 1H), 4.55 (p, J= 516.2018 7.3 Hz, 1H), 3.94 (s, 3H), 3.76 (s, 3H), 2.43 (s, 3H), 1.24 (d, J: 6.2 Hz, 3H), 1.12 (d, .1: 7.2 Hz, 3H). 19F NMR (376 MHz, CDC13) 8 —1]3.36, -11689. 1H NMR (400 MHz, CDC13) 512.07(s, 1H), 8,33 (d, J: 7.9 Hz, 1H), 7.97 (d, .1: 5.2 Hz, 1H), 7.29 (dd, J: 8.4, 6.7 Hz, 1H), 7.25 — 7.14 (m, 1H), 6,86 (d, .1: 5.2 Hz, 1H), 6.81 — 6.70 (m, 2H), HRMS-ESI (W) 6.56 (td, J: 8.3, 2.5 Hz, ([M+H]+) 1H), 6.50 (dd, .1 : 10.8, 2.5 Hz, 1H), 5.82(dq,J: 11.5, C 13311;???) 6.2 Hz, 1H), 4.78 (d,J= 10.1 515617237? féurfd Hz, 1H), 4.55 (p, .1: 7.2 Hz, 1H), 3.94 (S, 3H), 3.75 (S, 3H), 1.26 (d, J: 6.1 Hz, 3H), 1.12 (d, ,1: 7.2 Hz, 19F NMR (3 76 MHz, CDC13) 8—112.12(d,J: 7.5 Hz), _ 112.18 (d,J= 7.5 Hz), — 112.75 [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No1 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 812.08(s, 1H), 8.33 (d, .7: 7.9 Hz, 1H), 7.97 (d, J: 5.2 Hz, 1H), 7.32 (dd, J: 8.6, .8 Hz, 1H), 7.03 (dd, J: 8.3, 07 Hz, 1H), 6.86 (d, .1: HRMS-ESI (m/z) 5.2 Hz, 1H), 6.81 (td,J= +) 8.5, 2.8 Hz, 1H), 6.75 (dd, J : 9.7, 2.7 Hz, 1H), 6.62 4 calcd for 445 6.51 (111,2H), 5.69 (dq,J= C27H29F2N206, .0, 6.2 Hz, 1H), 4.76 (d, J 516.2021; found, : 9.8 Hz, 1H), 4.53 (p, .7: 16.2021 7.2 Hz, 1H), 3.94 (s, 3H), 3.84 (s, 3H), 2.26 (s, 3H), 1.27 (d, .1: 6.2 Hz, 3H), 1.07 (d, J: 7.2 Hz, 3H). 19F NMR (376 MHz, CDClg) 8 -112.84,_117.29. 1H NMR (400 MHz, CDC13) 812.04(s, 1H), 8.31 (d, .1: 7.8 Hz, 1H), 7.97 (d, J: 5.2 Hz, 1H), 7.32 (dd, J: 8.6, .7 Hz, 1H), 7.18 4 7.07 (m, 1H), 6.90 — 6.72 (m, 5H), HRMS-ESI (m/Z) .70 (dq,J= 11.7, 6.4 Hz, ([M+H]+) 1H), 4.64 (d, .7: 10.0 Hz, calcd for 1H), 4.54 (p, J: 7.2 Hz, C26H26F3N205, 1H), 3.94 (s, 3H), 2.27 (s, 504.1821; found, 3H), 1.29 (d, .1: 6.1 Hz, 504. 1818 3H), 1.09 (d, .1: 7.2 Hz, "’1? NMR (376 MHz, CDClg) 8-111.40(d,J= 7.6 Hz), — 112.58 (d,J= 7.6 Hz), — 116.32.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan CmNE.d. 853,: MP IR NMR (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 812.30 4 12.00 (m, 1H), 8.36 (d, .1: 8.0 Hz, 1H), 7.96 (dd, J: 5.2, 1.5 Hz, 1H), 7.39 — 7.12 (m, 6H), 6.89 — (Thin ?lm) m11§4f18115)m) 6.82 (m, 2H), 6.72 (dd, .1 : ,1“. 3373,2980, 11.3, 1.6 Hz, 1H), 5.82(dq,J 2938, 1737, calcd for = 9.8, 6.0 Hz, 1H), 4.56 (p, J 3:: 1650, 1576, C2(,H28FN205, : 7.3 Hz, 1H), 4.41 (d, .1: 1530, 1481, 77, found, 101 Hz, 1H), 3.92 (s, 3H), 1452 467.1974 223 (s, 3H), 1.26 (d, .1: 6.1 Hz, 3H), 1.09 (d, .1: 7.2 Hz, 19F NMR (376 MHz, CDC13) 8 -11895. 1H NMR (400 MHz, CDC13) 8 1207 (d, .1: 0.6 Hz, 1H), 8.34 (d, .1: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.29 — 7.23 (m, 2H), 7.21 (t,./: 79 HRMS-ESI (m/z) Hz, 1H), 7.00 — 6.93 (m, (Thin ?lm) ([M+H]+) 2H), 6.89 — 6.84 (m, 2H), 3377, 2983, 6.75 4 6.71 (m, 1H),5.814 1737, 1650, calcd for 448 5.68 (m, 1H), 4.60 — 4.49 (m, 1577, 1530, C26H2-F2N205, 1H), 4.39 (d, J: 10.1 Hz, 1510, 1481, 485.1883; found, 1H), 3.94 (s, 3H), 2.24 (s, 1453, 1440 485. 1877 3H), 1.26 (d, J: 6.1 Hz, 3H), 1.10 (d,.]= 7.2 Hz, 1"’1: 6 MHz, CDC13) 8 —1 15.56, —118.95.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No. (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 12.10 (s, 1H), 8.36 (d, .7: 8.0 Hz, 1H), 7.97 (d, .1: 5.1 Hz, 1H), 7.28 — 7.12 (m, 3H), 7.08 (d, ,1: 7.8 Hz, HRMS-ESI (m Z) 2H), 6.88 4 6.81 (m, 2H), (Thin ?lm) ([M+H]+) 6.71 (d, J: 11.2 Hz,1H), 3378,2982, .80 (dq,J= 12.1, 6.2 Hz, 2932, 1738, calcd for 449 1H), 4.55 (p, .1: 7.3 Hz, 1650, 1576, C27H30FN2057 1H), 4.38 (d, J: 10.1 Hz, 1530, 1481, 481.2133, found, 1H), 3.92 (s, 3H), 2.28 (s, 1452 33 3H), 2.22 (s, 3H), 1.26 (d, .1 : 6.1 Hz, 3H), 1.09 (d,J: 7.0 Hz, 3H).
"’F NMR (376 MHz, CDC13) —119.09. lH NMR (400 MHz, CDC13) 512.09(d,J= 0.6 Hz, 1H), 8.34 (d, J: 8.0 Hz, 1H), 7.98 (d, .1: 5.2 Hz, 1H), 7.24 (dd, J: 9.4, 5.5 Hz, 1H), 7.15 (t, HRMS-ESI (m ”2) J: 7.9 Hz, 1H), 6.90 — 6.78 (Thin ?lm) ([M+H]+) (m, 4H), 6.75 4 6.67 (m, 3373, 2982, 1H), 5.79 — 5.68 (m, 1H), calcd for 450 1737, 1651, 4.64 (d, J: 10.2 Hz, 1H), C27H29F2N205, 1577, 1530, 4.614 4.52 (m, 1H), 3.94 (s, 499.2039, found, 1482, 1453 3H), 2.39 (s, 3H), 2.24 (s, 499.2033 3H), 1.27 (d, J: 6.2 Hz, 3H), 1.13 (d, .1: 7.2 Hz, ”P NMR (376 MHz, CDCl;) -1 16.44, -1 18.17.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHZ, CDC13) (s, 1H), 8,33 (d, J: . - FIRMS-13810112) 8.0 Hz, 1H), 7.98 (d, .1: 52 5111111111111) ([M+H]+) Hz, 1H), 7.32 — 7.20 (m, 3375,2982, 4 4 2H), 6,9] — 6.70 (m, 5H), 2959, 1759, calcd for 451 5.86 4 5.76 (m, 1H), 4.70 (d, ‘1}; 1651, 1577, C26H26F3N205, x: J— 10.0 Hz, 1H), 4.62—4.51_ 1530, 1504,5 503.1788, found,, (m’ 1H)’ 3‘94 (5’ 3H)’ 2'254 5 1481 1453 503 1784 ‘ ” ‘ " (s, 3H), 1.29 (d, .1: 6.2 Hz, 3H), 1.12 (d, J: 7.3 Hz, 1H NMR (400 MHZ, CDC13) 512.08(d,J= 0.6 Hz, 1H), 8.33 (d, .1: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.31 _ 7.19 (m, 4H), 7.17 — 7.12 (m, 1H)” 7‘ 1 2 'Z'Ozfmgm)’ HRMS—ESI (m z) + 6.91 (dd, J7 9.3, 8..) HZ, ([M+H1 ) it: 1H), 6.86 (d, J: 5.2 Hz, calcd for 1H), 5177(dq, J: 10.2, 6.1 C2(,H28FN205, Hz, 1H), 4.59 -446 (m, 1H), 82; found, 3.99 (d, J: 10.2 Hz, 1H), 467.1969 394 (s, 3H), 2.23 (d, J: 1.9 Hz, 3H), 1.25 (d, .1 : 6.2 Hz, 3H), 0.97 (d, J: 72 Hz, "’F NMR (3 76 MHz, CDC13) —120.09.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS NMR No1 (‘0 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 612.08(s, 1H), 8.33 (d, J: 8.0 Hz, 1H), 7.97 (d, J: 5.2 Hz, 1H), 7.25 _ 7.20 (m, 1H), 7.12 - 7.01 (m, 2H), 6.93 - 6.82 (m, 2H), 6.57 (td, .1: HRMS-ESI(I1IZ) 8.3, 2.5 Hz, 1H), 6.50 (dd, J ([M+H]+) =10.9,2.5 Hz, 1H), 5.76 calcd for (dq,./: 103,61 Hz, 1H), C27H29FZNZO65 4.61 — 4.48 (m, 1H), 4.45 (d, 515.1993; found, J: 10.2 Hz, 1H), 3.94 (s, l 5. 1980 3H), 3.77 (s, 3H), 2.22 (d, .1 :19 Hz, 3H), 1.22 (d, J: 6.1 Hz, 3H), 1.07 (d, J: 7.2 Hz, 3H). 19F NMR (376 MHz, CDC13) -11333, -12033. 1H NMR (400 MHz, CDC13) 612.10(d,J= 0.6 Hz, 1H), 8.34 (d, .1: 8.0 Hz, 1H), 7.98 (d,J= 5.2 Hz, 1H), 7.31 — 7.27 (m, 2H), 7.24 — 7.15 (m, 4H), 7.15 4 7.06 (m, 3H), (Thin ?lm) 6.86 (d, J: 5.2 Hz, 1H), 5.81 3373,2980, (dq,J= 10.2, 6.1 Hz, 1H), 2938,1735 HRMS—ESI (m z) 4.57 4 4.46 (m, 1H), 4.02 (d, 1649,1576, ([M+H]+) J: 10.2 Hz, 1H), 3.94 (s, 1528,1495, calcd for 3H), 2.28 (s, 3H), 1.26 (d, J 454 1480,1451, C26H29N205, : 6.1 Hz, 3H), 0.96 (d, .1: 1332,1280, 449.2071; found, 7.2 Hz, 3H). 449.2063 1213,1144, 13CNMR(126 MHz, 1048, 799, CDC13)6171.68, 168.51, 733, 699 155.33, 148.70, 141.68, , 138.15, 136.55, 130.48, , 128.48, 127.93, 126.59, 109.38, 73.63, 57.57, 56.07, 47.85, .98, 19.24, 17.61. v) 00 La) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R N1er N0. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 612.11(d,.]: 0.6 Hz, 1H), 8.35 (d, J: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.29 — 7.24 (m, 4H), 7.20 — 7.15 (m, 3H), 7.03 (d, .1: 7.9 Hz, 2H), 6.86 (d, J: 52 Hz, (Thin ?lm) 1H), 5.80 (dq, J = 101,62 3367, 2981, Hz, 1H), 4.58 4 4.47 (m, 2938, 1736, 511112351??? Z) 1H), 4.02 (d, J = 100 Hz, 1649, 1576, 1H), 3.94 (s, 3H), 2.25 (s, 1529, 1480, calcd for 3H), 1.25 (d, .1: 6.1 Hz, 1451, 1333, C26H29N205, 3H), 1.01 (d, J : 72 Hz, 1281, 1263, 449.2071, found, 3H). 1213, 1146, 4492068 1048, 801, l3C1\11\4R(1261\4Hz, 734, 700 CDC13) 5 , 168.50, 155.33, 148.69, 141.41, , 138.28, 136.20, 130.47, , 128.74, 128.05, 127.90, 126.82, 109.36, 73.61, 57.44, 56.06, 47.86, 20.92, 19.23, 17.67.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No. (CC) (cm'l) (1H. 13C. 191:) 1H NMR (400 MHz. CDC13) 512.09(s. 1H). 8.34 (d. J: 8.0 Hz. 1H). 7.98 (d. J: 5.2 Hz. 1H). 7.25 — 7.21 (m. 2H). 7.18 — 7.13 (m. 2H). 7.04 (d. .1: 7.9 Hz. 2H). 7.00 — 6.92 (m. 2H). 6.86 (d. J: .2 Hz. 1H). 5.75 (dq.J= $2119“ 210191312). 9.9. 6.2 Hz. 1H). 4.59 4 4.47 1 7 . (m. 1H). 4.02 (d. J: 9.8 Hz. 2957. 1735. HRMS—ESHm/z) 1H) 3.94 (S 3H) 2‘26 (3 1649. 1576. ([M+H] ) 3H) 124 (d .1: 6.2 HZ 1528’ 1508’ calcd for 3H). 1.02 (d. J: 7.2 Hz. 456 1480. 1451.
,. C26H23FN205. 3H). 1529. 1280. 467.1977. found._ 115;” 1049’126. 1218 '"C NMR (126 MHz.5 74 8151800 ’ CDC13)5171.61. 168.52. 7129 1 161.66 (d. J: 2456 Hz). 155.35. 148.71. 140.40. 138.01. 137.20 .3 HZ). 136.40. 130.44. 129.53 ((1. J: 7.9 Hz). 129.22. 127.84. 115.57 (d.J=21.1 Hz).109.39. 73.44. 56.56. 56.07. 47.85. 20.92. 19.14. 17.66.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (300 MHz, CDC13) 6 12.07 (d, J: 0.6 Hz, 1H), 8.33 (d, J: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.33 — 7.19 (m, 7H), 6.96 — 6,88 (m, . - 2H), 6.87 (dd, .1: 5.3, 0.6 33713112191812) Hz, 1H), 5.78 (dq, J: 9.9, 2938’ 1736’ 6.1 Hz, 1H), 4.61 — 4.47 (m, 1649’ 1576’ HRMS—ESIEm z) 1H), 4.05 (d, .1: 10.0 Hz, 1529’ 1509’ ([M+H] ) 1H), 3.94 (s, 3H), 1.26 (d, J 1 1 = 6.2 Hz, 3H), 1.05 (d, J: 1480, 1452, calcd for 457 7 2 Hz 3H) 1330, 1280, CgngoFNgOs, ‘ ’ ‘ 13331123» WW 1048 815’ ‘ CDC13)6171.62, 16857, 7991732’ 161.59 (d,J:245.2 Hz), 6199 7 155.38, 148.73, 140.92, 140.43, 137.11 (d, 7:35 Hz), 130.39, 129.53 (d,J: 7.8 Hz), 128.88, 127.99, 127.08, 115.29 (d, .1=21.2 Hz), 109.43, 73.50, 57.03, 56.08, 4787, 19.21, 17.69.
[Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd. \\ MP IR NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (300 MHz, CDC13) 812.08(d,.]: 0.6 Hz, 1H), 8.33 (d, J: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.30 — 7.21 (m, 2H), 7.14 (d, J: 8.3 Hz, 2H), 7.09 (d, .1 : 8.2 Hz, 2H), 6.95 — 6.84 (m, 3H), (Thin ?lm) 5.76 (dq, J: 10.1, 6.1 Hz, 3366, 2979, 1H), 4.59 4 4.47 (m, 1H), 2939, 1736, HRMS-ESI (11272) 4.01 (d, J: 10.1 Hz, 1H), 1649, 1576, ([M+H]+) 3.94 (s, 3H), 2.29 (s, 3H), 1529, 1509, 1.25 (d, .1: 6.1 Hz, 3H), 1.04 C“1 d for 458 1481,1451, (d,J:7.2 Hz, 3H). 4 4 C26H28FN205, 1332’ 1264’ 467 1977 found p 1242, 1220, '467 11969 ° 3C NMR (126 MHz, 1159, 1049, ' CDC13) 5 171.61, , 815, 800, 161.53 (d,J=244.9 Hz), 770, 732 155.37, 148.71, 140.41, 137.93, 137.41 (d,J: 3.3 Hz), 136.72, 130.39, 129.54, 129.4] (d, J: 7.9 Hz), 127.82, 1 15.24 ((1, J: 21.3 Hz), 109.41, 73.55, 56.67, 56.07, 47.87, 20.96, 19.20, 17.68.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 6 12.07 (01, .1: 0.6 Hz, 1H), 8.32 (d, J: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.35 — 7.20 (m, 5H), 7.19 — 7.10 (m, 1H), 6.88 4 6.75 (m, 3H), (Thin ?lm) 5.88 — 5.77 (m, 1H), 4.58 — 3376, 2984, 4.47 (m, 1H), 4.42 (d, J: 2938, 1737, 10.1 Hz, 1H), 3.94 (s, 3H), 1649, 1576, £13151??? Z) 129 (d, J = 6.2 Hz, 3H), 1.00 1529, 1503, (d, J: 7.2 Hz, 3H). 1481, 1452, calcd for 459‘ 1~ 1327, 1281, F2N205, ”C NMR (126 MHz, 1263, 1243, 471.1726; found, CDC13) 5 171.56, 168.54, 1212,1146, 471.1726 162.05 (dd,./:172.5, 11.9 1050, 966, Hz), 161.09 4 159.28 (m), 849, 800, 155.35, 148.72, 140.42, 733, 699 , 130.41, 130.23 4 [29.63 (m), 128.61, 128.18, 127.03, 12446—12389 (m), 111.63 (d,J= 21.2 Hz), 109.41, 10454410381 (m), 72.76, 56.08, 49.36, 47.83, 18.90, 17.60.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 12.08 (01, J: 0.6 Hz, 1H), 8.33 (d, J: 8.0 Hz, 1H), 7.98 (d, J: 5.2 Hz, 1H), 7.26 — 7.21 (m, 1H), 7.20 — 7.15 (m, 2H), 7.07 4 7.01 (m, 2H), 6.88 — 6.85 (m, 1H), 6.84 — 6.74 (m, 2H), 5.86 — 5.72 (111, $210“ $9123). 1H), 4.59 4 4.48 (m, 1H), 29371 1737’ 4.39 (d, J: 9.9 Hz, 1H), 3.94 1649’ 1576’ HRMS-ESI (7172) (s, 3H), 2.26 (s, 3H), 1.28 (d, 1 7 + ([M+H] ) .14 6.5 Hz, 5H),i ’3 ’) 1.04 (d, .127 1529 1502 , , 7.2 Hz 3H). ’ 460 :b 14%1, 1f52, calcd for f: 1439, 1329, 59N205, 13C NMR (126 MHZ, 1281, 1264, 485.1885, found, CDC13)6171,55, 16855,, 1243 121] 485.1880 1147110501 161.99 (dd,J= 171.0, 11.9 966: 8497’ Hz), 160,02 (ch, .1: 170.8, 11.7 Hz), , 148.72, 801, 732 140.41, 136.92, 136.63, 130.43, 12997—12969 (m),129.24, 128.06, 124.73 — 124.42 (m), 111.58 (d,J= 17.7Hz), 109.40, 104.83— 103.37 (m), 72.82, 56.08, 48.91, 47.85, 20.95, 18.90, 17.67.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H,13C, 191:) 1H NMR (400 MHz, CDC13) 5120501.]: 06 Hz, 1H), 8.30 (d, J: 8.0 Hz, 1H), 7.98 (d,J= 5.2 Hz, 1H), 7.31 — 7.17 (m, 3H), 6.97 — 6.75 (m, . - 5H), 5,835.73 (m, 1H), $311“ $1913) 4.59 — 4.49 (m, 1H), 4.40 (d, 2939’ 1738’ ,7: 10.0 Hz, 1H), 3.95 (s, 1649, 1604, HRMS—ESI(/1IZ) 3’11}; 1%: Eg’j: 2:111: 1577, 1529, ([M+H]+) ’ ' ‘ ’ \ 3H) 1503’ 1481’ t calcd for 461 133% i422? C25H24F3N205, 13C NMR (126 MHz, 1264112427 489.1632, found, CDC13)6171.51, 168.59, 1223” 1160’ 4891624 162964 162.09 (m), 161.43 1050* 966’ 4159.21(m), 155.41, 84918107 148.74, 140.45, 135.75, 7132 1 , 129.73 (d,.1:8.0 Hz), 124.13 (dd, J: 15.2, 3.7 Hz), 115.43 (d,J=21.3 Hz), 11173 (d, J: 25.0 Hz), 109.46, 104.30 (t, .1: 25.8 Hz), 72.66, 56.10, 48.70, 47.86, 18.91, 17.67.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR N6. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.28 (d, .1: 5.4 Hz, 1H), 8.14 (d, J: 7.8 Hz, 1H), 7.26 — 7.15 (m, 4H), 6.94 (dddd, J = 24.3, 8.7, 6.9, 2.1 Hz, 5H), .76 4 5.63 (m, 3H), 4.55 (p, J: 7.3 Hz, 1H), 4.05 (d, J: 8.9 Hz, 1H), 3.92 (s, 3H), 2.06 (s, 3H), 1.32 (d, .1: 7.1 HRMS'ESIE’" Z) Hz, 3H), 1.22 (d, J = 6.2 Hz, ([M+H] ) calcd for 462 13 3;, C28H29F2N207, 3C NMR (101 MHZ, 31, found, CDC13) 6 171.92, 170.28, 543.1937. 162.91, 162.81, 162.77, 160.46, 160.37, , 144.13, 142.28, 136.93, 136.90, 136.54, 136.51, , 129.74, 129.70, 129.62,115.72,115.51, 115.43, 115.22, 109.60, 89.60, 73.10, 56.20, 55.58, 48.04, 20.85, 20.81, 18.94, 18.05.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.26 (d, .1: 5.4 Hz, 1H), 8.20 (d, J: 7.9 Hz, 1H), 7.28 — 7.17 (m, 4H), 7.02 — 6.89 (m, 5H), 5.76 — 5.66 (m, 3H), 4.55 (p, .1: 7.3 Hz, 1H), 4.04 (d, J: 9.7 Hz, 1H), 3.90 (s, 3H), 2.05 (s, 3H), 1.23 (d, .1: 6.1 Hz, SIW Z) 3H), 0.99 (d, J: 7.2 Hz, ([M+H] ) calcd for 4637 11 3;, C28H29F2N207, 3C NMR (101 MHZ, 543.1931, found, CDC13) 6 172.24, 170.26, 543.1937. 162.95, 162.90, 162.86, 160.51, 160.42, 160.28, 145.68, 143.98, 142.41, 136.94, 136.91, , , 129.62, 129.57, 129.54, 129.49, 115.79, 115.58,115.49,115.28, 109.58, 89.51, 73.04, 56.18, 5613,4805, 20.85, 19.14, 17.81.
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No, (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.26 (d, .1: 5.3 Hz, 1H), 8.21 (d, J: 7.9 Hz, 1H), 7.26 — 7.22 (m, 1H), 7.14 (dd, J: 8.6, 5.8 Hz, 1H), 6.94 (d, .1: .4 Hz, 1H), 6.89 4 6.77 (m, 4H), 5.73 (s, 2H), 5.62 (dq, J = 9.7.6.2 Hz, 1H), 4.56 (p, J : 7.2 Hz, 1H), 4.44 (d, .1: 9.8 Hz, 1H), 3.91 (s, 3H), 2.38 (s, 3H), 2.33 (s, 3H), 2.06 (s, 3H), 1.30 (d, .1: 6.2 Hz, 3H), 1.04 (d, J: 7.2 Hz, HRMS-ESI (m Z) 13C NMR (101 MHz, (Thin ?lm) ([M+H]+) CDC13) 6 172.30, 170.26, 3378, 2984, calcd for 162.91, 161.19 (d, .1: 245.6 464 1738, 1676, C30H33F2N207, Hz), 161.10 (d,J: 2450 1496, 1202, 571.2250; found, Hz), 160.28, 145.70, 143.98, 1003, 729 571.2265 142.43, 139.12 (d, .1: 7.4 Hz), 138.81 (d, .1: 7.5 Hz), 134.89 (d,J= 3.3 Hz), 134.39 (d, J: 3.2 Hz), 12937 (d, .1: 8.2 Hz), 128.75 (d,J= 8.3 Hz), 117.41 (d,J= 20.9 Hz), 117.10 (d, J: 20.9 Hz), 112.94 (CLJ: 20.9 Hz), 112.63 (d,J= 20.8 Hz), , 8952,7429, 5619, 4807, 4640,2086, 2020, .12,18.82,17.86.
"’F NMR (376 MHz, CDC13) -116.57, —117.03. v) 0 La) [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.26 (d, .1: 5.4 Hz, 1H), 8.23 (d, J: 7.8 Hz, 1H), 7.32 — 7.20 (m, 8H), 6.93 (d, J: .4 Hz, 1H), 5.79 (dq, J: .2, 6.1 Hz, 1H), 5.73 i .70 (m, 2H), 4.50 (p, J: 7.2 Hz, 1H), 3.98 (d, J: 10.2 HRMS-ESI (m z) Hz, 1H), 3.89 (s, 3H), 2.05 (Thin ?lm) ([M+H]+) (s, 3H), 1.27 — 1.22 (m, 3379, 2962, 21H), 0.78 (d, J: 7.2 Hz, calcd for 465 2:; 1 73 7, 1676, 3H).
\ C36H47NZO77 ‘ 1158821172591, 61933781 found 13C NMR 1 ( 101 MHz 619.3388 ’ CDC13) 6 172.43, 170.23, 162.84, 160.24, 149.56, 149.37, 145.69, , 142.62, 138.80, 138.26, 127.69, 127.65, 125.60, 125.33, 109.49, 89.55, 73.71, 5725,5615, 4804, 34.36, 34.31, 31.30, 20.85, 19.34, 17.50.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No, (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.26 (d, .1: 5.4 Hz, 1H), 8.22 (d, J: 7.8 Hz, 1H), 7.28 — 7.19 (m, 4H), 7.16 — 7.06 (m, 4H), 6.93 (d, J: 5.4 Hz, 1H), 5.78 (dq, .1: 10.2, 6.1 Hz, 1H), 5.72 (d, J: 0.9 Hz, 2H), 4.51 (p, J: 7.2 Hz, 1H), 3.98 (d, .1: 10.2 Hz, 1H), 3.89 (s, 3H), 2.81 (dh, J (Thin ?lm) Wilfg?ff/Z) = 10.6, 6.9 Hz, 2H), 2.05 (s, 3378, 2959, 3H), 1.24 (d, .1: 6.1 Hz, 1737, 1676, calcd for 3H), 1.18 (dd, J : 13.6, 6.9 1506, 1202, C34H43NZO7, Hz, 12H), 0.81 (d, J: 7.2 1044, 1004, 591.3065; found, Hz, 3H). 828, 731 77 13CN1\4R(1011V1Hz, CDC13)6 172.42, 170.24, 162.85, 160.24, 147.29, 147.13, , 143.92, 142.63,139.19,138.71, 127.95, 127.92, 126.75, 126.48, 109.49, 89.55, 73.66, 57.39, 5616,4805, 33.65, 33.61, 23.99, 23.97, 23.93, .86, 19.33, 17.57.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd.
MASS N1VJR No1 (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.27 (d, .1: 5.3 Hz, 1H), 8.23 (d, J: 7.8 Hz, 1H), 7.07 — 6.90 (m, 7H), 5.82 — 5.67 (m, 3H), 4.54 (p, J: 7.2 Hz, 1H), 3.90 (s, 3H), 2. 17 (t, .1: 11.4 Hz, 12H), 2.06 (s, 3H), FIRMS-13810772) 1.28 — 1.20 (m, 4H), 0.93 (d, (Thin ?lm) ([M+H]+) .1: 7.2 Hz, 3H). 3388, 2979, 1756, 1677, calcd for 467 13C NMR (101 MHz, 1503, 1203, C32H39N207, CDC13) 5 172.41, 170.25, 1044, 1004, 563.2752, found, 162.84, 160.23, 145.69, 970, 731 64 143.90, 142.67, 139.25, 139.11, 136.78, 136.34, 134.93, 134.51, 129.90, 129.62, 129.39, 129.38, 125.30, 125.08, 109.48, 89.55, 73.49, 57.1 1, 56.16, 4812,2086, 19.87, 19.80, 19.32, 1929,1924, 17.80. 1HNMR (400 MHz, CDC13) 8.41 (d, J: 7.7 Hz, 1H), 8.30 (61, .1: 5.4 Hz, 1H), 7.32 — 7.21 (m, 1H), 7.14 (dd,J= 8.5, 5.8 Hz, 1H), 6.99 (d,J= .5 Hz, 1H), 6.83 (ddd,./: .6, 10.1, 7.6 Hz, 4H), 5.62 ESIMS 777 Z 541.2 :57?”Haw/[J (dq, J = 9.6, 6.1 Hz, 1H), 468 ([M+H]+) 4.62 4 4.50 (m, 1H), 4.43 (d, , J: 9.7 Hz, 1H), 3.88 (s, 3H), 2.38 (s, 3H), 2.36 (s, 3H), 2.31 (s, 3H), 1.29 (d, .1: 6.2 Hz, 3H), 1.03 (d, .1 : 7.2 Hz, ”P NMR (376 MHz, CDCH) 2, -11696.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.43 (d, .1: 7.9 Hz, 1H), 8.32 (d, J: 5.4 Hz, 111), 7,26 (d, J: 12.1 Hz, 8H), 6.98 (d, .1: 5.4 Hz, 1H), 5.78 (dq, .1: .1, 6.1 Hz, 1H), 4.56 4 4.43 (m, 1H), 3.97 (d, J = HRMS—ESI(7172) 1337512” 1:11) j i: (3’ 3,11)”‘3 (5’ " )’ ' ( " 7 (Thin ?lm) ([M+H]+) 12.6 Hz, 21H), 0.77 (d, J: 3379, 2962,, calcd for 7.2 Hz, 3H).2 469 1772, 1677, C35H45N20‘” 1508 1 198 1 71,1 1 589.3272; found, 1”C NMR (101 MHz, 589.3289 6172.32, 168.88, 162.23, 159.40, 149.55, 149.37, 146.64, 141.60, 138.76, 138.25, 137.43, 127.70, 127.65, 125.60, 125.32, 109.67, 73.75, 57.22, 56.25, 47.81, 34.35, 34.31, 3131,3130, 2073,1932, 17.69.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No, (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.42 (d, .1: 7.6 Hz, 1H), 8.32 (d, .1: 5.5 Hz, 1H), 7.22 (dd, J: 8.3, 2.5 Hz, 4H), 7.15 4 7.04 (m, 4H), 6.98 (d, .1: 5.5 Hz, 1H), 5.78 (dq,.1: .1, 6.1 Hz, 1H), 4.54 4 4.43 (n1, 1H), 3.97 (d, J: .2 Hz, 1H), 3.89 (s, 3H), HRMS-ESI (m z) 2.82 (dp, J: 11.9, 6.9 Hz, (Thin ?lm) +) 2H), 2.37 (s, 3H), 1.23 (d, J 3379, 2960, : 6.2 Hz, 3H), 1.18 (dd, J: 1772, 1677, calcd for 470 14.7, 6.9 Hz, 12H), 0.80 (d, J 1509, 1201, C33H41N206, = 7.2 Hz, 3H). 1175, 1047, 561.2959; found, 73 1 561.2977 13C NMR (101 MHz, CDC13)6172.31, 168.89, 162.23, 159.41, 147.28, 147.13,146,64,141.61, 139.14, 138.70, 137.43, 127.96, 127.92, 126.75, 126.47, 109.68, 73.70, 57.36, 56.25, 4783, 33.64, 33.61, 23.97, 074, 19.31, 17.75. 1H NMR (400 MHZ, CDC13) 8 8.48 4 8.37 (m, 1H), 8.32 (Thin ?lm) SI (m Z) (d, J: 5.4 Hz, 1H), 7.09 4 3379, 2978, ([M+H1+) 6.90 (n1, 7H), 5.74 (dq, J: 1771, 1676, calcd for 10.0, 6.1 Hz, 1H), 4.58 4 471 1505, 1450, C31H37N2067 4.46 (m, 1H), 3.98 4 3.83 (m, 1310, 1199, 533.2646, found, 4H), 2.38 (s, 3H), 2.17 (dd, J 1050, 907, 533.2659 = 12.4, 11.0 Hz, 12H), 1.22 (d, .1: 6.1 Hz, 3H), 0.92 (d, J: 7.1 Hz, 3H).
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.26 (d, .1: 5.4 Hz, 1H), 8.22 (d, J: 7.9 Hz, 1H), 7.38 HRMS-ESI (m/Z) (m, 1H), 7.13 (m, 1H), 6.94 ([M+H], ) (d, J = 5.4 Hz, 1H), 6.61 _ (Thin ?lm) i M . 6.47 (m, 4H), 5.87 (dq, .14 3382, 2982, calcd for , 9.7, 6.2 Hz, 1H), 5.72 (s, 1737, 1677, F2N209, 1501, 1202 603.2149, found,2 _ 2H), 4.84 (d, J— 9.6 Hz, 1H), 46444.48 (m, 1H), 60, 216,3' 3 3.90 (s, 3H), 3.82 (s, 3H), 3.74 (s, 3H), 2.06 (s, 3H), 1.22 (61, .1: 6.2 Hz, 3H), 1.03 (d, J : 7.2 Hz, 3H). 1H NMR (400 MHz, CDC13) HRMS-ESI(/1Iz) 5 8,77 , 8.42 (m, 1H), 8.42 , (Thin ?lm) ([M+H]+) 8.15 (m, 1H), 7.26 4 7.15 (m, 3367, 2985, 4H), 7.06 4 6.86 (m, 5H), C2110d for 473 1749,1694, 5.844566 (m, 3H), 5.374 C H RN 0 1506, 1201, ”$816225? 13111121 5.19 (m, 1H), 4.13 44.03 (m, 1130, 828 1H), 4.04 4 3.83 (m, 3H), 597.1672 2.09 4 1.99 (m, 3H), 1.30 4 1.16 (m, 3H).
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (300 MHz, CDC13) 8.28 (t, .1: 7.2 Hz, 2H), 7.35 — 7.12 (m, 10H), 6.94 (d, J: 5.4 Hz, 1H), 5.86 (q, .]= 6.3 Hz, 1H), 5.75 — 5.68 (m, 2H), 4.62 (p, .1: 7.2 Hz, 1H), 3.90 (s, 3H), 2,06 (s, Wilfg?fy/Z) 3H), 1.75 (s, 3H), 1.16 (d, J : 6.3 Hz, 3H), 1.12 (d, .1: calcd for 72 Hz, 3H).
C29H33N207, 521.2282; found, ”C NMR (101 MHz, 521.2292, CDC13) 5 172.27, 170.20, 162.88, 160.26, 146.57, 145.66,145.11,143.98, 142.56, 128.18, 128.09, 127.92, 127.40, , 126.11, 109.53, 89.54, 75.94, 56.17, 50.41, 48.23, 23.95, .84,18.13,15.97.
'H NMR (400 MHz, CDCH) 6 8.41 (d, J: 4.6 Hz, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.37 (dd, .1: 8.5, 6.7 Hz, 1H), . 7.12(dd,J:8.3, 6.7 Hz, $319“ £19123 HRMS-ESIfm/z) 1H), 6.99 (d, J = 5.5 Hz, 1769’ 1736’ ([M+H] ) 1H), 6.63 4 6.44 (m, 4H), * ’ 5.86 (dq, J: 9.5, 6.2 Hz, 1677, 1598, calcd for 475 :3; 1H), 4.83 (d, J — 9.5 Hz,_ 1500, 1277, C29H31F2N203, 1H) 4 62 2 4 45 (m” 1H) 1192,1174, 573.2043;f0und, ', g ’, ” "90(31 JH)’ 382(5’ 3H)?, 1151 1033 573 2055 9’53 7 ' 3.73 (s, 3H), 2.38 (s, 3H), 1.21 (d, J: 6.2 Hz, 3H), 1.01 (d, .1: 7.2 Hz, 3H). 191: NMR (376 MHz, CDC13) 8 -113.49,_113.81.
[Annotation] an None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd. MP 1R NMR No. (CC) (cm'l) (1H, 13C, 191:) 1:1 mixture of diastereomers.
. H NMR (500 MHz CDC13), (Thm ?lm) ’ 8,52 2 8.46 (m, 1H), 8.20 33827 3028, HRMS-ESI W Z) + (d,J— 7.6 Hz, 1H), 8.16(d, 2984’ 1736’ ([M+H] ) J: 7.5 Hz, 1H), 7.33 — 7.10 476 1161;? 1:2: calcd for (m, 11H), 5.86 , 5.74 (m, 1310’ 1261’ C28H31N207, 3H), 4.61 — 4.48 (m, 1H), 104; 967* 507.2126; found, 410 — 4.04 (m, 1H), 4.02 (3, 91031825 5072141 3H), 2.06 (s, 3H), 2.05 (s, 728’ 703’ 3H), 1.31 (d, J: 7.1 Hz, 1 3H), 1.28 — 1.20 (m, 3H), 0.91 (d, J: 7.2 Hz, 3H). 1H NMR (400 MHz, CDC13) 8.30 (d, .1: 5.5 Hz, 1H), FEMS-E8199 7‘%0§d2éi%’%i125”1354( _ )1 _ (Thin ?lm) ([M+H]+) '3 ’ Z’ ‘ 7.30 (m, 4H), 7.03 (d, J: 5.5 ”76 2985 477 3328’ 176‘9’ calcd for Hz, 1H), 5.76 (dq, J: 8.8, 17,8” 1674’ C29H2-N4O6, 6.1 Hz, 1H), 4.60 — 4.52 (m, 31505 1 527.1925, found, 1H), 4.20 (d, J: 9.0 Hz, 527.1931 1H), 3.95 (d, .1: 9.9 Hz, 1H), 3.92 (s, 3H), 2.39 (s, 3H), 1.25 (d, J: 6.2 Hz, 3H), 1.08 (d, .1: 7.2 Hz, 3H) 1H NMR (400 MHz, CDC13) 8.38 (d, J: 7.9 Hz, 1H), FIRMS-138101272) 812 7 8'29 (m’ 1H)” 7'56 (9’ . + J— 7.9 Hz, 2H), 7.52 (d,J— $317113? ([M+H] ) 8.5 Hz, 2H), 7.44 4 7.36 (m, calcd for 4H), 7.01 (dd, J: 5.5, 3,5 478 17727 17397 CZQHZ'FGNZOG, Hz, 1H), 5.88 — 5.79 (m, 1677, 1617, 613.1768; found, 1H), 4.59 — 4.53 (m, 1H), ()13. 178 4.22 (d, .1: 9.2 Hz, 1H), 3.90 (s, 3H), 2.38 (s, 3H), 1.28 — 1.22 (m, 3H), 0.98 (d, J = 7.2 Hz, 3H).
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP 1R NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.38 (d, .1: 8.7 Hz, 1H), 8.32 4 8.29 (m, 1H), 79701, J: 8.3 Hz, 2H), 7.93 (d, J: HRMS-ESI(717Z) 8.2 Hz, 2H), 7.38 (d, .1: 8.3 ([M+H] ) Hz, 2H), 7.34 ’) : 8.4 Hz, (Thin ?lm) 2H), 7.00 (d, J— 5.5 Hz, 3379, 2980, calcd for 479 1H), 5.85 (dq, J— 9.6, 6.1_ 1772, 1714, C33H37N2016, ,, . ,4.5944.50(m, 1678, 1508 621.2443,16und, 1H), 4.38—4.30(m,4H),, , 6212451' 4.21 (d, J: 9.7 Hz, 1H), 3.89 (s, 3H), 2.38 (s, 3H), 1.36 (t, J: 7.3 Hz, 6H), 1.25 (d, J: 6.3 Hz, 3H), 0.98 (d, J: 7.1 Hz, 3H). 1H NMR (400 MHz, CDC13) 8.28 4 8,24 (m, 1H), 8.20 (d, .1: 7.8 Hz, 1H), 8.00 4 7.92 (m, 4H), 7.42 — 7.31 (m, Wiggly/Z),7 4H), 6.95 (d, J = 5.4 Hz, ([ 1 ) (Thin ?lm) 1H), 5.85 (dp, .1 : 9.4, 7.2, 3379, 2983, calcd for 6.6 Hz, 1H), 5.73 — 5.67 (m, 1714, 1676, C34H36N2011, 2H), 4.56 (p, J: 6.9 Hz, 1607, 1507 651.2548; found, 1H), 4.39 4 4.28 (m, 4H), 651.2560 422 (d,J: 9.7 Hz, 1H), 3.91 (d, J: 1.5 Hz, 3H), 2.06 (s, 3H), 1.37 (t, J: 7.2 Hz, 6H), 1.27 (d, J: 6.2 Hz, 3H), 0.98 (d, J = 7.1 Hz, 3H).
[Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd.
MASS NMR No, (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.26 (d, .1: 5.4 Hz, 1H), 8.22 (d, J: 7.9 Hz, 1H), 7.34 (d,J= 8.3 Hz, 1H), 7.09 (d, .1: 8.0 Hz. 1H), 6.94 (11.1: .4 Hz, 1H), 6.88 4 6.82 (m, (Thin ?lm) HRMS-ESI(/1Iz) 2H), 6.81 (s, 1H), 6.76 (d, J 4,“ 3379, 2939, = 2.0 Hz, 1H), 5.86 (dq, J: ([M+Na]_) calcd for 481 .,,.”,1, 1737, 1677, C30H32C12N2N309, ,,(lg/1..., , 9.7, 6.2 Hz, 1H), 5.72 (s, , , 1490, 1247, 657.1377, found, , 2H), 4.84 (d, .1: 9.6 Hz, 1202, 1033 657.1387 1H), 4.57 (p, J: 7.2 Hz, 1H), 3.90 (s, 3H), 3.83 (s, 3H), 3.74 (s, 3H), 2.06 (s, 3H), 1.22 (d, J: 6.2 Hz, 3H), 1.04 (d, .1: 7.2 Hz, 1H NMR (400 MHz, CDCH) 6 825 (1, .1: 6.6 Hz, 2H), 7.34 (dd, J: 85,69 Hz, 1H), 7.13 (111,7: 79,67, 4.7 Hz, 1H), 6.93 (d, .1: 5.4 Hz, 1H), 6.60 — 6.36 (m, HRMS-ESI (m/Z) (Thin ?lm) 4H), 5.90 (dq, J= 102,62 ([M+H]+) 3380, 2981, Hz, 1H), 5.73 (s, 2H), 4.83 1736, 1677, calcd for (d, J: 10.1 Hz, 1H), 4.63 — 1597, 1500, C32H3‘F2N209, 4.48 (m, 1H), 4.08 — 3.79 (m, 1274, 1202, 631.2462; found, 7H), 2.06 (s, 3H), 1.47 (1, .1: 1003 63 1.2461 6.9 Hz, 3H), 1.40 (1, J : 6.9 Hz, 3H), 1.23 (d, J: 6.2 Hz, 3H), 1.04 (d, .1: 7.2 Hz, ”P NMR (376 MHz, CDCl;) 8 -113.76,-114.20.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.29 4 8.19 (m, 2H), 7.31 (d, J: 8.3 Hz, 1H), 7.11 (d, J: 8.2 Hz, 1H), 6.94 (d, J: - HRMS-ESI m ]+() ) 5.4 Hz, 1H 6.86 — 6.73 , m, ghm ?lm) 3H), 6.72)(d, .1: 2.0 Hz, ”38129801 1H), 5.89 (dq, J= 99,62 1736’ 1677’ cam for 483 Hz, 1H), 5.73 (s, 2H), 4.83 1591,1491, C32H37C12N209, (d 1:98HZ 1H) 457( 1247,1201, 663.1871; found, J;7 2H2 1H) 4 (1)5;3 $31 1040 6611877 (m, 7H), 2.06 (s, 3H), 1.47 (t, J: 6.9 Hz, 3H), 1.39 (t, J: 6.9 Hz, 3H), 1.23 (d, J : 6.1 Hz, 3H), 1.06 (d, J: 7.2 Hz, 1H NMR (400 MHz, CDC13) 8.29 4 8.18 (m, 2H), 7.30 (d, .1: 7.8 Hz, 1H), 7.13 (d, J: 7.7 Hz, 1H), 6.92 (d, J: .4 Hz, 1H), 6.67 — 6.57 (m, mm ?lm). - HRMS'ESU'" Z) 3H), 6.54 (s, 1H), 5.93 (dq, .1 ([Mm] ) = 10.3, 6.1 Hz, 1H), 5.72 (s, 484 $22133: calcd for 1H), 5.72 (s, 1H), 4.90 (d, J 16761 15047 C34H43N2‘OI), : 10.1 HZ, 1H), 4.55 (13, J: 12001 1043’ 623.2963; found, 71 Hz, 1H), 4.04 — 3.81 (m, 1 623.2962 7H), 2.26 (s, 3H), 2.23 (s, 3H), 2.05 (d, .1: 1.8 Hz, 3H), 1.47 (t, J: 7.0 Hz, 3H), 1.39 (t, J: 7.0 Hz, 3H), 1.23 (d, J: 6.] Hz, 3H), 0.99 (d, J : 7.2 Hz, 3H).
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd.
MASS NMR No. (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz. CDC13) 8.39 (d, .1: 6.9 Hz.1H). 8.29 (d. .1: 5.4 Hz. 1H), 7.05 — 6.92 (m. 3H), 6.89 (dd, J: 8.1. 2.1 Hz. 1H). 6182 (dddd.
HRMS-ESI (/17 Z) .1: 15.8. 8.3. 4.0. 2.1 Hz.
([M+H]+) 3H). 5.72 (dq,J= 9.7, 6.1 calcd for Hz. 1H). 4.65 — 4.48 (m. 1H).
C29H31F2N208, 3.99 (c1. .1: 9.8 Hz. 1H). 3.88 573 .205 1; found, (s, 3H). 3185 (s, 6H). 2.38 (s. 573 .2044 3H). 1.24 (d. J: 6.1Hz, 3H). 1.02 (61.7: 7.1 Hz, 19F NMR (376 MHz,CDC13) 8 -13720, -13768.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No. (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz. CDC13) 8.43 (d. .1: 7.8 Hz. 1H). 8.28 (d. J: 5.4 Hz. 1H). 7,21 (d.J= 8.5 Hz. 1H). 7.17 — 7.09 (m. 1H). 6.96 (d. .]= 5.5 Hz. 1H). 6.79 - 6.57 (m. 4H). .63 (dq. J: 9.7. 6.1 Hz. 1H). 4.64 — 4.50 (m. 1H). 4.38 (d. .1: 9.9 Hz. 1H). 3.86 (s. 3H). 3.73 (s. 3H). 3.71 (s.
SI (m/Z) 3H). 2.38 (s. 3H). 2.35 (s.
([M+H]+) 3H). 2.31 (s. 3H). 1.29 (d. .1 calcd for :61 Hz. 3H). 1.01 (61.1: C31H3‘N208, 7.1 Hz. 3H). 565.2542; found. 13C NMR (101 MHz.
CDC13)6172.25. 168.81. 162.28. 159.43. . 157.67. 146.63. 141.55. 137.98. 137.71. 137.44. 131.95.131.46.128.85. 128.22. 116.24. 116.03. 111.25. 110.94. 109.75. 74.80. 56.24. 55.05. 47.92. 46.23. 20.71. 20.36. 20.28. 18.88.1808. 1HNMR (400 MHz. CDC13) 8.26 (d.J: 5.4 Hz. 1H). 8.21 (d. J: 7.8 Hz. 1H). 7.06 _ 6.92 (m. 3H). 6.92 _ 6.74 HRMS-ESI (m 2) (m. 4H). 5.84 _ 5.61 (m. 3H).
([M+H]+) 4.56 (p. J: 7.3 Hz. 1H). 4.00 calcd for (d.J= 9.8 Hz. 1H). 3.91 (s.
C30H33FZNZO‘L 3H). 3.86 (s. 6H). 2.06 (s. 603.2157; found. 3H). 1.25 (d. J: 6.2 Hz. 603 .2150 3H). 1.02 (d. J: 7.2 Hz. 191: NMR (376 MHz. CDC13) 8 -13720. -137.72.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H. 13C. 191:) 1H NMR (500 MHz. CDC13) 8.44 (s. 1H). 8.31 (01.7: .4 Hz. 1H). 7.33 ((1.1: 8,5 ,, Hz. 1H). 7.10 (d. J: 8.4 Hz.
(Thin ?lm) W151i???) 1H). 6.98 (d. .1: 5.5 Hz. 3383. 2938. 1H). 0.42 4 0.34 (m. 4H). 2837. 1770. calcd for 5.85 (dq. J: 9.7. 0.2 Hz. 1733. 1077. C31H34N20m. 1H). 4.81 (d. J: 9.8 Hz. 1009. 1580. 597.2443; found. 1H). 4.59 4 4.49 (m. 1H). 1505. 1453 597.2438 3.90 (s. 3H). 3.82 (s. 3H). 3.75 (s. 3H). 3.74 (s. 3H). 3.73 (s. 3H). 2.38 (s. 3H). 1.21 (d. J : 0.2 Hz. 3H). 0.99 (d. J: 7.2 Hz. 3H). 1H NMR (500 MHz. CDC13) 8.44 (s. 1H). 8.31 (d, J: .4 Hz. 1H). 7.31 (d. .1: 7.7 Hz. 1H). 710(01. ./:8.1 Hz. 1H). 0.98 (d. J— 5.5 Hz.
HRMSESI (m/Z) 1H). 0.09 4 0.05 (m. 1H).
(Thin ?lm) ([M+H]+) 0.05 4 0.02 (m. 2H). 0.00 4 3382 2937 calcd for 489 1771’ 1733’ 6.54 (m. 1H), 5.89 (dq,J= 16777 15727 C31H3TN208, 98, 6.2 HZ, 1H). 490((1, J: 0 5* [452’ 505.2544. found. 9.8 Hz. 1H). 4.58 4 4.48 (m. 1 505.2541 1H). 3.90 (s. 3H). 3.82 (s. 3H). 3.73 (s, 3H). 2.38 (s. 3H). 2.27 (s. 3H). 2.25 (s. 3H). 1.21 (d. J: 0.2 Hz. 3H). 0.95 (d. J = 7.2 Hz.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS N1VJR No. (cm ) (1H7 13c:1 19F) 1H NMR (500 MHz, CDC13) 6 8.45 (s, 1H), 8.32 (61,7: .4 Hz, 1H), 7.22 (d, J: 2.1 Hz, 1H), 7.03 (d, .1: 2.2 Hz, 1H), 6.98 (d, .1: 5.5 Hz, 1H), 6.93 (ddd, .1: 8.3, 2.3, HRMS-ESI (m z) 0.8 Hz, 1H), 6.89 (ddd,J= (Thin ?lm) ([M+H]+) 8.2, 2.2, 0.8 Hz, 1H), 6.73 (d, 3383, 2937, calcd for .1: 8.3 Hz, 1H), 6.67 (d, .1: 490 2836, 1772, C31H3’N208; 8.2 Hz, 1H), 5.85 (dq, J: 1735, 1678, 565.2544; found, 10.0, 6.2 Hz, 1H), 4.95 (d, J 1502, 1453 565.2538 : 10.0 Hz, 1H), 4.58 4 4.46 (m, 1H), 3.90 (s, 3H), 3.82 (s, 3H), 3.72 (s, 3H), 2.38 (s, 3H), 2.25 (s, 3H), 2.21 (s, 3H), 1.22 (d, J: 6.1 Hz, 3H), 0.95 (d, J: 7.1 Hz, 1H NMR (500 MHz, CDC13) for both isomers ofa 1:1 mixture of reomers d 8.40 (s, 1H), 8.38 (s, 1H), 8.32 (d, J: 5.0 Hz, 1H), 8.31 (d, J: 5.3 Hz, 1H), 7.21 4 HRMS-ESI (m z) 7.13 (m, 2H), 7.03 — 6.83 (m, (Thin ?lm) ([M+H]+) 12H), 5.76 — 5.63 (m, 2H), 3382, 2985, .04 (d, .1: 11.9 Hz, 1H), 2941, 2840, calcd for 491 5.02 (d,.]: 11.2 Hz, 1H), 1771, 1736, C29H31F2N2085 4.63 — 4.47 (m, 2H), 3.93 (d, 1677, 1578, 573 .2043; found, .1: 2.0 Hz, 3H), 3.92 (s, 3H), 1508, 1479 573.2042 3.914 3.89 (m, 6H), 3.80 (d, J: 1.7 Hz, 3H), 3.76 (d,J= 1.6 Hz, 3H), 2.39 (s, 3H), 2.38 (s, 3H), 1.31 (d, .1: 7.2 Hz, 3H), 1.29 — 1.22 (m, 6H), 1.03 (d, J: 7.2 Hz, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H, 13C. 191:) 1H NMR (500 MHz. CDC13) for the major isomer ofa 2:1 mixture ofdiastereomers d 8.44 (s. 1H), 8.32 (d, J: 5.5 Hz, 1H), 7.18 (dd, .1: 9.7.
HRMS-ESI (m z) 3.0 Hz. 1H), 6.99 (d. .1: 55 (Thin ?lm) ([M+H]+) Hz, 1H). 6.96 (dd, J = 9.5. 3383. 2941, 3.0Hz,1H),6.87—6.79(m, calcd for 492 2839. 1770. 2H). 6.76 (dd, .1: 9.0. 4.6 CnH~ RN70 1736. 1677, 5732645 £61156 Hz, 1H). 6.72 (d, J = 4.6 Hz. 1592. 1495 573 23045 ’ 1H). 5.87 (dq, J: 9.6, 6.2 Hz. 1H). 4.88 (d. .1: 9.6 Hz. 1H). 4.60 4 4.53 (m, 1H), 3.90 (s. 3H), 3.83 (s, 3H). 3.74 (s, 3H). 2.38 (s. 3H). 1.23 (d. J: 6.2 Hz. 3H), 1.02 (d. J = 7.2 Hz. 3H).
[Annotation] Mel.Chan None set by an [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd.
MASS N1V1R No1 (1H7 13c:1 19F) 1H NMR (500 MHz, CDC13) for 1:1 mixture of diastereomers 8 8.26 (t, J : .1 Hz, 4H), 7.07 (ddd, J: 13.9, 79, 111 Hz, 2H), 7.00 — 6.89 (m, 6H), 6.85 (td, .1: 8.8, 8.0, 113 Hz, 2H), 6.78 — 6172(m, 4H), 5.75 — 5,71 (m, 4H), 5.71 2 5.62 (m, 2H), .12 (dd, J: 13.7, 98 Hz, 2H), 4.63 — 4.47 (m, 2H), 3.91 (s, 3H), 3.90 (s, 3H), 3.89 (s, 3H), 3.86 (s, 3H), 3.84 (s, 3H), 3.83 (s, 3H), 3.81 (s, 3H), 3.80 (s, 3H), 3.74 (s, 3H), 3.71 (s, 3H), 2.06 (s, 6H), 1.32 (d, J: 7.1 112,311), 1.26 (d, .1 : 6.0 Hz, HRMS-ESI (m 2) 3H), 1.24 (d, J: 6.2 Hz, ([M+H1+) 3H), 1.00 (d, J: 7.2 Hz, calcd for 3H).
C32H39N2011, 48, found, 13C NMR (126 MHz, 627.2546 CDC13) for 1:1 mixture of diastereomers 8 172.36, 171.98, 170.28, 162.82, 162.78, 160.26, 16023, 152.82, 152.78, 152.71, 147.42, 147.31, 147.19, 147.11, 145.68, , , 142.70, 142.64, 135.14, 134.87, 134.78, 134.61, 123.66, 123.62, 121.05, 120.97, 120.46, 120.33, 110.74, 110.61, 110.55, 109.44, 99.98, 89.63, 89.59, 73181, 7375, 60.40, 60.36, 60.31, 60.25, 56.17, 56.16, 55164, 55.59, 48.18, 48.12, 4196, 41.83, 29.28, .88, 1886,1871, 18.41, 17.91.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. n . :\§» \\\\\ ‘\‘\1 MP MASS NMR No, \'\'\x ‘ ~‘ (‘0 (1H7 13c:1 19F) 1H NMR (500 MHz, CDC13) for 1:1 mixture of diastereomers 8 8.40 4 8,28 (m, 2H), 8.26 (dd, J: 5.3, 3.7 Hz, 2H), 7.07 (ddd, J: 13.1, 8.0, 1.2 Hz, 2H), 7.03 2 6.89 (m, 6H), 6.88 — 6.80 (m, 2H), 6.75 (td, J= 56,28 Hz, 4H), 5.81 4 5.72 (m, 4H), 5.72 — 5.62 (m, 2H), .12 (dd, J: 13.4, 9.8 Hz, 2H), 4.54 (dp, .1: 17.6, 7.2 Hz, 2H), 3.89 (s, 3H), 3.89 (s, 3H), 3.88 (s, 3H), 3.86 (s, 3H), 3.84 (s, 3H), 3.83 (s, 3H), 3.81 (s, 3H), 3.80 (s, 3H), 3.74 (s, 3H), 3.71 (s, 3H), 2.54 (pd, .1: 7.0, 4.2 Hz, 2H), 1.32 (d, J: 7.1 Hz, 3H), 1.26 (d, J: 6.1 Hz, SI (m2) 3H), 1.24 (d, J = 6.2 Hz, ([M+H]+) 3H), 1.14 (d, .1: 3.1 Hz, calcd for 6H),1.13(d,J= 3,1Hz, C34H43N2O11, 6H), 1.00 (d, J: 7.2 Hz, 655.2861; found, 3H). 655.2858 13C NMR (126 MHz, CDC13) for 1 :1 mixture of diastereomers 6 176.26, 176.24, 172.37, , , 162.73, 160.25, 160.21, , 152.78, 152.70, 147.42, 147.32, 147.19, 147.11, 145.53, 144.22, 144.16, 142.27, 135.14, 134.88, 134.79, 13462, 123.66, 123.62, 121.06, 120.97, 120.47, 120.33,110.76,110.74, 110.61,110.55,109,39, 99.98, 90.02, 89.95, 73.79, 73.73, 6040, 60.36, 60.31, 60.26, 56.12, 56.10, 55.64, 55.59, 48.18, 48.12, 41.96, 4182,3387, 3385,1885, 18.68,18.41,17,91.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by an Cmpd. n . :\§» \\\\\ ‘\‘\1 MP MASS N1VJR No, \'\'\x ‘ ~‘ (‘0 (1H, 13c:1 19F) 1H NMR (500 MHz, CDC13) for 1:1 mixture of diastereomers 8 8.45 (s, 2H), 8.32 (d, J: 3.9 Hz, 1H), 8.31 (d, J = 3.9 Hz, 1H), 7.07 (ddd, J: 12.2, 8.0, 1.3 Hz, 2H), 7.01 — 6.89 (m, 6H), 6.89 — 6.79 (m, 2H), 6.75 (td, J: 6,8, 1.5 Hz, 4H), 5.73 2 .60 (m, 2H), 5.12 (d, J: .1 Hz, 1H), 5.10 (d,J= 9.5 Hz, 1H), 4.61 4 4.52 (m, 1H), 4.52 4 4.44 (m, 1H), 3.91 (s, 3H), 3.90 (s, 3H), 3.89 (s, 3H), 3.86 (s, 3H), 3.83 (s, 3H), 3.83 (s, 3H), 3.81 (s, 3H), 3.80 (s, 3H), HRMS-ESI (m z) 3.73 (s, 3H), 3.72 (s, 3H), ([M+H]+) 2.39 (s, 3H), 2.38 (s, 3H), 1.30 (d, J: 7.1 Hz, 3H), 1.27 calcd for 495 — 1.22 (m, 6H), 0.98 (d, J: C31H37N20m, 7.1 Hz, 3H). 597.2443; found, 597.2434 13C NMR (126 MHz, CDC13) for 1:1 mixture of diastereomers 6 172.26, ,168.91,162.22, 162.18, 159.42, , 152.82, 152.77, 15270, 147.40, 147.32, 147.18, 147.11, 146.63, 141.62, 137.45,137,41,135.11, 134.85, 134.76, 134.60, 123.66, 123.64, , 120.97, 120.48, 120.33, 110.74,110.61,110.55, 109.65, 7383, 73.78, 60.40, 60.38, 60.31, 60.28, 56.28, 56.26, 55165, 55.63, 55.58, 48.01, 4791,4181, 20.76, 18.84, 18.68, 18.48, 18.07.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. m . :\§» \\\\ \\ ‘\‘ \1 MP MASS NMR Nu \'\'\x ‘ ~‘ (‘0 (1H7 13c:1 19F) 1H NMR (500 MHz, CDC13) for 1:1 mixture of diastereomers 8 8.43 (s, 2H), 8.32 (d, J: 4.4 Hz, 1H), 8.31 (d, J: 44 Hz, 1H), 7.39 — 7.30 (m, 2H), 7.13 (t,./: 9.0 Hz, 2H), 7.05 — 6.86 (m, 10H), 5.74 — 5.58 (m, 2H), .09 (d, .1: 9.7 Hz, 1H), 5.06 (d, J: 9.1 Hz, 1H), 4,53 (dq, J: 15.5, 75 Hz, 2H), 3.91 (s, 3H), 3.90 (s, 3H), 3.83 (s, 3H), 3.79 (s, 3H), 370 (s, 3H), 3.68 (s, 3H), 2139(s, 3H), 2.38 (s, 3H), 2.30 (s, HRMS-ESI(/1Iz) 3H), 2.29 (s, 3H), 2.25 (s, ([M+H]+) 6H), 1.30 — 1.23 (m, 9H), 0.92 (d, J: 7.2 Hz, 3H). calcd for C31H3’N208; 13C NMR (126 MHz, 565.2544, found, CDC13) for 1:1 mixture of 565.2538 diastereomers 8 172.25, 171.70, , 162.23, 162.17, 159.44, 15940, 156.93, 156.89, 156.82, 156.75, 146.64, 146.57, 141.65, 141.59, 13742, 134.11, , 133.86, ,131.2O,131114, 131.04, 130.95, 130.03, 129.76, 129.70, 126.87, 126.70, 126.65, , 123.81, 109.65, 74.38, 74.32, 60.31, 6023, 60.20, 56.29, 56.27, 47.98, 47.84, 41.65, .75,19.06,18.90,18.41, 18.00, 16.68, 1647.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd.
MASS NMR No. (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) for 1:] mixture of diastereomers 8 8.50 4 8,23 (m, 4H), 7.13 — 6.92 (m, 8H), 6.86 (t, J: 7.1 Hz, 2H), 6.73 , 6.63 (m, 4H), 5.77 , .58 (m, 2H), 4.61 (t, J: 9.4 Hz, 2H), 4.49 (dp, J: 26.5, 7.1 Hz, 2H), 3.90 (s, 3H), 3.89 (s, 3H), 3.79 (s, 3H), 3.78 (s, 3H), 3.76 (s, 3H), 3.75 (s, 3H), 2.38 (d, J: 0.9 Hz, 6H), 228 (s, 3H), 2.26 HRMS-ESI (m/Z) (s, 3H), 2.20 (s, 3H), 2.18 (s, ([M+H]+) 3H), 1.27 (dt, .1: 6.4, 3.2 Hz, 9H), 0.96 (d, J: 7.1 Hz, calcd for 497 3H).
C31H37N208, 565.2544; found, [73C NMR (101 MHz, CDC13) for 1:1 e of diastereomers 8 172.28, 171.77, 168.85, 162.24, 159.41, 157.72, 157.55, 146.61, 141.63, , 140.51, 140.12, 137.47, 126.12, 126.08, 125.91, 125.42, 120.51, 120.39, 119.92, 119.76, 109.64, 108.32, 7477, 74.71, 56.26, 55.45, 53.40, 48.08, 47.90, 47.55,20.72,18.81, 18.67, 18,29,17.98,11.80,11,73, 11.43.
[Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.35 (d, .1: 5.5 Hz, 1H), 8.30 (d, J: 5.4 Hz, 1H), 7.07 (ddd, J: 8.2, 5.7, 2.2 Hz, 1H), 7.00 (d, .1: 5.5 Hz, 1H), 6.86 4 6.72 (m, 3H), .70 — 5.62 (m, 1H), 4.85 (d, J: 9.4 Hz, 1H), 4.62 — 4.54 (Thin ?lm) (m, 1H), 3.97 (d, .1: 2.3 Hz, 3384, 2942, HRMS-ESI (mz) 3H), 3.91 (s, 3H), 3.83 (d, J 1771, 1737, ([M+H]+) = 2.0 Hz, 3H), 2.38 (s, 3H), 1677,1501, 1.23 (d,.]:6.1Hz,3H),1.11 ca Cldfor 498 1475, 1430, (d, J: 7.2 Hz, 3H). '3 C29H29F4N2087 1308’ 1200’ 609 1855 found 1~ 100, 6091851 ° JCNMR(126MHZ, 1057, 950, ' ‘ CDC13) 8 172.04, 168.90, 908, 731 162.27, 159.48, , 147.34 4 146.78 (111), 146.60, 143.34, 141.37, 137.50, 129.96 — 129.37 (111), 123.61 — 122.42 (111), 110.81 (d,J= 13.5 Hz), 110.68 (d, .1: 13.2 Hz), 109.78, 72.31, 61.44— 60.78(m), 56.31, 4789, 4240,2074, 18.77, 18.11.
[Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (H, 13C, 19F) 1H NMR (400 MHz, CDC13) 8.43 (s, 1H), 832 (61,7: .4 Hz, 11117117 6.83 (m, 7H), 5.66 (dq, J: 10.0, 6.1 Hz, 1H), 4.57 — 4.48 (m, 1H), 4.45 (d, .1: 10.0 Hz, 1H), 3.90 (s, 3H), 2.38 (s, . 3H), 2.35 (s, 3H), 2.29 (3, gm min) 3H), 2.27 (s, 3H), 2.25 (s, 1771, 1734, ([M+H]+) 3H)” 0 94 (d’ J: 7 2 Hz’ 1 ' , ‘ , 6:: 1677, 1504, calcd for 3H)., 490 5 g, 1451, 1310, C31H3'N206’ ‘ 1198 1175 « 1147’ 104,1 533.2646; found, 13C NMR (126 MHz, 9081806” 1 CDC13)6172.41, 168.91, 7130 1 162.25, 159.41, 146.64, 141.58, 139.12, 138.59, 137.44, 135.40, , 133.59, 133.35, 130.56, 130.27, 128.60, 127.91, 127.20, 126.91, 109.68, 74.87, 56.27, 47.90, 47.34, 21.28, 21.22, 20.75, 19.79, 19.73, 18.86, 17.98.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No, (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.42 (s, 1H), 8.31 (d,./: .5 Hz, 1H), 7.18 (d, J: 7.9 Hz, 1H), 7.12 (d, J: 8.6 Hz, 1H), 6.98 (d, J: 5.5 Hz, 1H), 6.96 4 6.85 (m, 4H), .66 (dq, J: 9.9, 6.2 Hz, 1H), 4.57 — 4.48 (m, 1H), . - 4.43 (d, .1: 10.0 Hz, 1H), (Thm 111m) 3.90 (s, 3H), 2.38 (s, 3H), 3384, 2938, SI (m/Z) 2 34 (S 3H) 2 30 (S 3H) 1771* 1735’ ([NHHD 2,25 (s: 3H): 2,21 (s: 3H): calcd for 1.28 (d, J: 6.1 Hz, 3H), 0.96 1 1:; i283 ? 7 C31H3‘N206, (d, J: 7.1 HZ, 3H). 1198, 1174, 533.2646; found,,, 1 100 1043 13 9083804 ’ 533.2642 'CNMR(126 MHZ, 7’3 0 ’ CDC13) 5 172.30, 168.92, 162.24, 159.41, 146.64, 141.59, 137.43, 136.50, 136.40, 136.19, , 135.84, 135.52, 131.49, 131.15, , 127.14, 126.81, 126.59, 109.67, 74.83, 5627, 47.89, 46.82, .84, 20.81, 20.76, 20.13, .07, 18.92, 1803. ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.43 (d, .1: 7.9 Hz, 1H), 8.32 (d, J: 5.4 Hz, 1H), 7.13 — 6.98 (m, 4H), 6.91 (dd,J= .3, 2.8 Hz, 1H), 6.81 (dtd, .1: 12.5, 8.2, 2.7 Hz, 2H), .57 (dq, J: 9.6, 6.1 Hz, 1H), 4.61 — 4.51 (m, 1H), 4.46 (d, .1: 9.6 Hz, 1H), 3.90 (s, 3H), 2.38 (s, 3H), 2.34 (s, 3H), 2.29 (s, 3H), 1.32 (d, J (Thin ?lm) : 6.2 Hz, 3H), 1.02 (d, J: 3379, 2983, HRMS-ESI(I112) 7.2 Hz, 3H). 1770, 1738, ([M+H]+) 1677, 1496, 13C NMR (126 MHz, calcd for 501 1453, 1310, CDC13) 5 172.15, 168.90, C H“ RN06 1199,1176, 54i92134115ff0unéi 162.31, 161.35 (d, J: 243.7 1148, 1043, 541 21146 3 Hz), , 146.68, 909, 808, ‘ ' 141.44, 140.63 (d, J : 6,5 729 Hz), 140.14 (d, J: 6.7 Hz), 137.47, 132.40 (d, 1:31 Hz), 132.06 (d, .1: 2.0 Hz), 132.01 (d,J= 3.1 Hz), 131.69 (d, J: 7.8 Hz), 114.83 (d, .1: 22.2 Hz), 114.37 (61.1: 22.3 Hz), 113.65 (d,J= 20.8 Hz), 11337 (d, J: 20.6 Hz), 109.75, 74.02, 56.28, 47.77, 47.72, 20.75, 19.42, 19.35, 18.83, 18.00.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.42 (d, .1: 7.6 Hz, 1H), 8.32 (d, J: 5.4 Hz, 1H), 7.01 — 6.97 (m, 1H), 6.96 — 6.91 (m, 2H), 6,88 (d, J: 9.3 Hz, 1H), 6.86 4 6.81 (m, 1H), 6.70 (dt, J: 9.0, 3.5 Hz, 1H), 6.65 (dt, J: 9.0, 3.5 Hz, 1H), 5.83 (dq, .1: 12.0, 6.1 Hz, 1H), 4.69 (d, J: 10.3 Hz, 1H), 4.57 (p, J: 7.3 Hz, 1H), 3.90 (s, 3H), 3.74 (3, (Thin ?lm) HRMS-ESI(I1IZ) 6H), 2.38 (s, 3H), 1.30 (d, J 3378, 2940, ([M+H]+) = 6.2 Hz, 3H), 1.02 (d, J: 1770, 1738, 7.1 Hz, 3H). 6616d for 502 1677, 1498, C29H~1F7N708 11 1207, 1176, "C NMR (126 MHz, 573 2074331611118 1151,1037, #321047 ’ CDC13)6172.11, , 816, 730 ‘ ' , 159.42, 155.73 (01, J = 1.8 Hz), 155.57 (d,J= 2.0 Hz), 15519 (d, J: 238.6 Hz), 154.96 (d,.1:238.7 Hz), 146.63, 141.51, 137.44, 127.90 (d, J: 15.8 Hz), 12766 (d, .1: 16.2 Hz), 116.23 (61,1: 24.8 Hz), 115.96 (d,J=24.9 Hz), 115.16, , 113.214 112.82 (m), 109.69, 72.01, 56.28, 55.71, 47.85, 43.39, .75, 18.96, 18.05.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.42 (s, 1H), 8.32 (d,./: .4 Hz, 1H), 7,29 (1,,/: 8.7 Hz, 1H), 7.16 (t, J: 8.5 Hz, 1H), 6.99 (d, J: 5.5 Hz, 1H), 6.65 4 6.55 (m, 3H), 6.51 (dd, J: 12.0, 2.6 Hz, 1H), 5.78 (dq, J: 12.1, 6.2 Hz, 1H), 4.66 4 4.52 (m, 2H), 3.90 (s, 3H), 3.75 (s, . 3H), 3.72 (s, 3H), 2.38 (5, $719“ $218) 3H), 1,27 (d, .1: 6.2 Hz, 1770’ 17‘36’ HRMS-ESI(I112) 3H), 1.06 (d, J: 7.2 Hz, ’ 4’ ([M+H]+) 3H). 1676,1623, 1585, 1:06, calcd for 503 ”C NMR (126 MHZ, 1444’ 1310’ C29H31F2N208’ CDC1~) 5 172 11‘ 168 91 1195, 1175, 573.2043, found, 1 ~ , 162.24, 161.24 ((11.1,24517_ 1154,1031,, 44, HZ) 16101(d J:2459 907, 832, , - ,_ » Hz), 159.72 (d, J— 11.2 Hz), 803, 729 15946 (d, J: 11.3 Hz), 159.44, 146.60, 141.51, 137.44, 129.90 (d,J=5.4 Hz), 12934 (d, J = 5.6 Hz), 11960 (d, .1: 14.6 Hz), 119.45 (d,J: 15.0 Hz), 110.13(d,J=3.0Hz), 109.85 7109.61 (m), 101.99 7 101.44 (m), 72.26, 56.28, 55.50, 55.46, 47.88, 41.64, .75, 18.93, 18.13.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.40 (s, 1H), 8.3] (d,./: .4 Hz, 1H), 7.54 (d, J: 8.0 Hz, 1H), 7.30 (d, J: 7.8 Hz, 1H), 7.12 (d, J: 8.0 Hz, 2H), 7.04 4 6.97 (m, 3H), 6.01 — 5.91 (m, 1H), 4.99 (d, (Thin ?lm) £1191??? 33325361?) 348496 3381, 2942, HRMS—ESI (m z) ;H ; 81 (5’ 3 )1 3‘ (S “7H) 238 (S'3 1772, 1728, ([M+H]+) ’ 3_ * 1 3H), 1.24 (d, J— 6.2 Hz, 1679 1508 ‘ ’ calcd for 3H), 0,98 (d, .1: 7.2 Hz, 504 1456, 1417, , ,, C31H31F6N203, 3H). 1327,1242, 673.1979; found, 1172 112] 13 10331904” 673.1985 ‘CNMR(126MHZ, 739 ’ CDC13) 5 , 162.27, 159.47, 157.54, 157.39, 146.61, 141.44, 137.49, 132.44, 130.44 4 129.46 (m),117.00, 109.74, 107.51 (d, J: 25.6 Hz), 99.99, 71.95, 56.28, 55.73, 55.69, 47.82, 43.70, 20.73, 18.89, 17.97. 1H NMR (400 MHz, CDC13) 8.42 (d, J: 7.9 Hz, 1H), 8.32 (d, .1: 5.5 Hz, 1H), 6.99 (d, J: 5.5 Hz, 1H), 6.66 4 6.53 (m, 4H), 6.45 (ddt, J = (Thin ?lm) Wiggiff’ Z) 14.8, 10.5, 2.3 Hz, 2H), 5.67 3375, 2939, (dq, J: 99,61 Hz, 1H), 1770, 1677, calcd for 4.62 — 4.49 (m, 1H), 3.94 (d, 0 5 1592, 1509, C26H31F2N2Og, .1: 9.9 Hz, 1H), 3,90 (s, 3H), 1195, 1136, 573.2043, found, 3.76 (s, 3H), 3.75 (s, 3H), 1059, 731 34 2.38 (s, 3H), 1.25 (d, J: 7.6 Hz, 3H), 1.02 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) 53—11067, -11 1.17. ation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.42 (d, .1: 7.7 Hz, 1H), 8.32 (d, J: 5.4 Hz, 1H), 6.98 (d, J: 5.5 Hz, 1H), 6.45 (dd, .1: 6.5, 2.3 Hz, 4H), 6.28 (dt, .1: 17.4, 2.3 Hz, 2H), .74 (dq,J= 10.3, 6.1 Hz, 1H), 4.59 — 4.48 (m, 1H), (Thin ?lm) $111353??? Z) 3.93 4 3.86 (m, 4H), 3.76 (s, 3375, 2938, 6H), 3.74 (s, 6H), 2.38 (s, 1770, 1677, calcd for 3H), 1.28 — 1.22 (m, 3H), 321593, 1203, C3|H37N20|(), 0.97 (d, J: 7.2 HZ, 3H). : 1152, 1064, 597.2443, found, 731 597.2442 13C NMR (101 MHz, CDC13) 6 172.26, 168.86, 162.29, 160.95, 160.78, 159.43, 146.64, 143.47, 143.25, 141.64, 137.47, 109.69, 106.48, 106.26, 9854,9844, 72.91, 58.21, 56.26, 55.30, 55.28, 47.92, .73, 19.23, 18.01.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan ed set by Mel.Chan Cmpd. m . :\8 \\\\ \\ ‘\‘ \1 MP MASS N1VJR Nu \'\'\ \5‘ (‘0 (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.42 (d, .1: 7.9 Hz, 1H), 8.32 (d, J: 5.4 Hz, 1H), 6.98 (d, J: 5.5 Hz, 1H), 6.69 (d, .1: 1.5 Hz, 2H), 6,64 (dt, .7: 4.2, 1.9 Hz, 2H), 6.54 (t, .1: 1.9 Hz, 1H), 6.49 (t, J: 1.9 Hz, 1H), 5.73 (dq, J: 10.3, 6.1 Hz, 1H), 4.59 4 4.47 (m, 1H), 3.89 (s, 4H), 3.75 (s, SI (mt) 3H), 3.73 (s, 3H), 2.38 (s, (Thin ?lm) ([M+H]+) 3H), 2.28 (3,311), 2.25 (s, 3384, 2939, 3H), 1.23 (d, J: 6.1 Hz, 1771, 1677, calcd for 507 3H), 0.93 (d, J: 7.1 Hz, 1593, 1508, C31H37N208, l 172, 1 152, 565.2544; found, 1066, 732 565.2540 13CN1\4R(1011V1Hz, CDC13) 5 172.30, 168.86, 162.27, 159.77, 159.64, 159.43, 146.64, 142.75, 142.51, 141.67, 139.73, 139.31, 137.46, 121.35, 121.29, 112.68, 111.36, 110.95, 109.68, 73.23, 57.88, 56.26, 55.15, 55.13, 47.91, 29.30, 21.67, 21.60, 20.73, 19.27, 17.96.
[Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan ed set by Mel.Chan Cmpd.
MASS N1VJR No1 (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.40 (d, .1: 7.9 Hz, 1H), 8.31 (d, J: 5.4 Hz, 111), 7,06 — 6.94 (m, 3H), 6.80 (ddd, J = 7.7,61, 1.7 Hz, 2H), 6.73 (dd, .1: 14.2, 1.6 Hz, 2H), .79 (dq,J= 10.1, 6.1 Hz, 1H), 4.60 — 4.47 (m, 1H), 3.96 (d, .1: 10.1 Hz, 1H), 3.89 (s, 3H), 3.79 (s, 3H), HRMS-ESI (m/Z) 3.79 (s, 3H), 2.38 (s, 3H), (Thin ?lm) ([M+H]+) 2. 14 (s, 3H), 2.11 (s, 3H), 3376,2939, calcd for 1.24 (d, J : 6.4 Hz, 311), 0.93 508 1771, 1678, C31H3‘N208, (d, J: 7.2 Hz, 3H). 1508, 1201, 565.2544; found, 1040, 734 565.2538 13C NMR (101 MHZ, CDC13)6172.31, 168.86, 162.28, 159.44, 157.84, 157.65, 146.62, 141.65, 140.39, 140.28, 137.48, 130.75, 130.48, 125.19, 124.79, 119.76, 119.68, 109.94, 109.85, 109.69, 73.32, 57.89, 56.26, 55.29, 47.93, 29.30, 20.73, 19.30, 17.97,15.80,15175.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. n . :\§» \\\\\ ‘\‘\1 MP MASS N1VJR No. \'\'\ \5‘ (‘0 (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.40 (d, .1: 7.9 Hz, 1H), 8.32 (d, J: 5.4 Hz, 1H), 7.04 — 6.91 (m, 5H), 6.86 (dt, J= SI (m z) 7 Hz, 2H), 5.63 (dq, ,1 (Thin ?lm) ([M+H]+) : 94,61 Hz, 1H), 4.64 4 3373,2939, 4.51 (m, 1H), 3.92 (d, J: 9.5 1770, 1676, calcd for 509 Hz, 1H), 3.90 (s, 3H), 3.84 1513, 1276, C29H31F2N2O8, (s, 3H), 3.82 (s, 3H), 2.38 (s, 1201, 1026, 573.2043, found, 3H), 1.22 (d, J: 6.2 Hz, 731 573 .2033 3H), 1.05 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) -13420, —134.64. 1H NMR (400 MHz, CDC13) 68.43 (s, 1H), 831 (d,./: .5 Hz, 1H), 7.12 4 6.94 (m, 5H), 6.70 (dd, J: 14.1, 8.4 Hz, 2H), 5.69 (dq, J: 9.9, 6.1 Hz, 1H), 4.60 4 4.49 (m, 1H), 3.89 (s, 3H), 3,87 (d, J = 10.6 Hz, 1H), 3.77 (s, 3H), 3.74 (s, 3H), 2.38 (s, 3H), HRMS-ESI(I11Z) 2.16 (s, 3H), 2.14 (s, 3H), (Thin ?lm) +) 1.21 (d, J: 6.1 Hz, 3H), 0.95 3386, 2939, calcd for (d, .1: 7.1 Hz, 3H). 510 1771, 1677, N208, 1504, 1201, 565.2544, found, 13CN1\4R(1011V1Hz, 1176, 732 565.2526 CDC13) 6 172.30, 168.86, 162.26, 159.43, 156.52, 156.35, 146.63, 141.69, 137.46, 133.70, 133.57, 130.50, 130.37, 126.79, 126.37, 126.10, 125.87, 110.05, 109.92, 109.67, 73.70, 56.26, 56.23, 55.31, 55.29, 47.94, 20.73, 19.29, 18.08, 16.32, 16.25.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd. m . :\§» \\\\\ ‘\‘\1 MP MASS N1VJR Nu \'\'\ \a‘ (‘0 (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 6 8.50 4 8.35 (m, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.07 (d, J: 3.0 Hz, 1H), 6.97 (d,J= .5 Hz, 1H), 6.87 (d, .1: 3.0 Hz, 1H), 6.80 4 6.60 (m, 4H), 5.91 (dq, J: 9.9, 6.1 Hz. 1H), 4.93 (d, J: 10.0 Hz, 1H), 4.62 4 4.45 (m, 1H), 3.89 (s, 3H), 3.81 (s, HRMS-ESI (7112) 3H), 3.74 (s, 3H), 3.71 (s, (Thin ?lm) ([M+H]+) 3H), 3.70 (s, 3H), 2.38 (s, 3387, 2940, 3H), 1.23 (d, J: 6.1 Hz, 1771, 1678, calcd for 511 3H), 0.97 (d, J: 7.1Hz, 1499, 1223, C31H37N2010, 1046, 808, 597.2443; found, 732 597.2410 13CN1\4R(1011V1Hz, CDC13)8 172.29, , 162.24, 159.40, 153.47, 153.45,151.89,151.77, 146.63, 141.73, 137.43, 130.69, 116.44, 115.43, 112.14,112.11,111.84, 111.55, 109.63, 73.04, 56.33, 56.29, 56.25, 55.68, 55.59, 47.96, 930, 2073, 1891,1813 [Annotation] Mel.Chan None set by Mel.Chan ation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.43 (d, .1: 8.0 Hz, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7,05 (d, J: 8.3 Hz, 1H), 7.01 — 6.94 (m, 2H), 6.90 (d, .]= 2.7 Hz, 1H), 6.82 (d, .1 : 2.7 Hz, 1H), 6.63 (ddd, J: 18.7, 8.4, 2.7 Hz, 2H), 5.65 (dq, J: .1, 6.1 Hz, 1H), 4.59 4 4.49 (m, 1H), 4.45 (d, J: .0 Hz, 1H), 3.89 (s, 3H), (Thin ?lm) HRxais?ff Z) 3.73 (s, 3H), 3.73 (s, 3H), 3381, 2939, 2.38 (s, 3H), 2.32 (s, 3H), 1771, 1677, calcd for 2.27 (s, 3H), 1.31 (d, J: 6.1 1502, 1200, CngyNZOg, Hz, 3H), 0.97 (d, .1: 7.1 Hz, in: 1175, 1043, 565.2544; found, 3H). 731 565.2543 (101 MHz, CDC13)6 172.26, 168.85, 162.28, 159.43, 157.92, 157.89, 146.64, , 140.31, 139.86, 137.47, 131.43,131.10,128.88, 128.61, 114.65, 113.69, 111.27,111.11,109.70, 74.59, 56.26, 55.19, 47.90, 47.86, 2930,2073, 19.29, 19.25, 18.90, 17.99.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS N1VJR No, (‘0 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.27 (d, .1: 5.4 Hz, 1H), 8.23 (d, J: 7.8 Hz, 1H), 6.94 (d,J= 5.4 Hz, 1H), 6.60 (dddd, .1: 13.2, 108, 3.9, (Thin ?lm) HRMS-ESI (m Z) 1.8 Hz, 4H), 6.45 (ddt, .1: 3381, 2940, ([M+H]+) 13.9, 10.5, 2.3 Hz, 2H), 5.76 1740, 1675, — 5.63 (m, 3H), 4.57 (p,J= calcd for 1592, 1505, 7.3 Hz, 1H), 3.95 (d, .1: 10.0 C30H33FZNZO97 1200, 1134, Hz, 1H), 3.90 (s, 3H), 3.77 1045,829, 603.2149, found, (s, 3H), 3.75 (s, 3H), 2.06 (s, 603.2137 730 3H), 1.26 (d, .1: 6.1 Hz, 3H), 1.04 (d, J: 7.2 Hz, "’F NMR (376 MHz, CDC13) -110.67, —111.20.
'H NMR (400 MHz, CDCH) 8 8.26 (d, J: 5.4 Hz, 1H), 8,23 (d, J: 7.8 Hz, 1H), 6.93 (d, .1: 5.4 Hz, 1H), 6.46 (dd, J: 7.4, 22 Hz, 4H), 6.28 (dt, J = 16.6, 2.2 Hz, 2H), .814 5.68 (m, 3H), 4.55 (p, J: 7.2 Hz, 1H), 3.96 — 3.86 (Thin ?lm) SI (m/Z) (m, 4H), 3.76 (s, 6H), 3.74 3382, 2937, ([M+H]+) (s, 6H), 2.06 (s, 3H), 1.26 (d, 1737, 1675, calcd for J: 6.2 Hz, 3H), 0.99 (d,J: 514 1593, 1457, C32H39N2O11, 7.2 Hz, 3H). 1202, 1150, 627.2548; found, 1062, 829, 627.2555 [73C NMR (101 MHz, CDC13) 5 172.37, 170.22, 162.89, , 160.79, 160.25, 145.70, , 143.51, 143.26, 142.65, 109.51, 106.49, 106.24, 98.54, 98.43, 89.57, 72.87, 58.24, 56.17, 55.30, 55.28, 48.14, 20.85, 19.25, 17.84.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS N1VJR No. (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.27 (d, .1: 5.4 Hz, 1H), 8.23 (d, .7: 7.8 Hz, 1H), 6.93 (d, J: 5.4 Hz, 1H), 6.70 (s, 2H), 6.65 (dt, .1: 5.7. 1.9 Hz, 2H), 6.55 (t, .1: 1.7 Hz, 1H), 6.50 (t, J: 1.7 Hz, 1H), .80 — 5.66 (m, 3H), 4.54 (p, .1: 7.2 Hz, 1H), 3.93 4 3.87 (m, 4H), 3.75 (d, J: 7.3 Hz, HRMS-ESI (m/Z) (Thin ?lm) 6H), 2.29 (s, 3H), 2.25 (s, ([M+H]+) 3382, 2937, 3H), 2.06 (s, 3H), 1.24 (d, .1 1738, 1676, calcd for : 6.1 Hz, 3H), 0.95 (d, J: 1594, 1504, N209, 7.1 Hz, 3H). 1293, 1202, 595.2650; found, 1152 595.2647 l3C 1 MHz, CDC13) 6 172.41, 170.22, 162.88, 160.25, 159.77, 159.65, 145.70, 143.93, 142.79, 142.70, 142.52, 139.73,139.31,121.35, 121.30,112.69,111.36, 110.92, 109.50, 89.57, 73.19, 57.91, 56.16, 55.15, 55.14, 48.13, 29.30, 21.67, 21.60, .85, 19.29, 17.79.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan MASS NMR No, (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.26 (d, .1: 5.4 Hz, 1H), 8.21 (d, J: 7.8 Hz, 1H), 7.05 — 6.96 (m, 2H), 6.93 (d, J: .4 Hz, 1H), 6.81 (td,J= 7.4, 1.6 Hz, 2H), 6.76 (d, .1: 1.6 Hz, 1H), 6.72 (d, J: 1.6 Hz, 1H), 5.79 (dq, J: 10.1, 6.2 Hz, 1H), 5.72 (d, .1: 1.4 Hz, 2H), 4.55 (p, J = 7.2 Hz, 1H), 3.97 (d, J: 10.2 Hz, HRMS-ESI (m Z) 1H), 3.90 (s, 3H), 3.80 (s, (Thin ?lm) ([M+H]+) 3H), 3.79 (s, 3H), 2.14 (s, 3382, 2936, 3H), 2.11 (s, 3H), 2106(s, 1737, 1676, calcd for 516 3H), 1.26(d,.1: 6.2 Hz, 1505, 1202, C32H39N209, 3H), 0.94 (d, J: 7.2 Hz, 1040, 969, 595.2650, found, 730 595.2639 [73C NMR (101 MHz, 6172.43, 170.21, 162.89, , 157.85, 157.65, 145.68, 143.94, 142.67, 140.44, , 130.75, 130.48, 125.19, 124.78, 119.75, 119.67, 109.94, 109.86, 109.52, 89.56, 73.28, 57.91, 56.17, 55.29, 5528,4816, 20.85, 19.32,17.82,15.80,15.75. ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.27 (d, .1: 5.4 Hz, 1H), 8.23 (d, J: 7.9 Hz, 1H), 7.04 — 6.92 (m, 5H), 6.87 (q, J= HRMS-ESI(I17Z) 8.7 HZ, 2H), 5.72 (s, 2H), (Thin ?lm) ([M+H]+) 5.64 (dq, .1: 9.5, 6.2 Hz, 3382,2984, 1H), 4.65 — 4.48 (m, 1H), calcd for 517 1739, 1675, 3.93 (d, J: 9.7 Hz, 1H), 3.91 CmHvaNyOo \ 1512, 1275, 603‘ 2129: 1‘6und (s, 3H), 3.84 (s, 3H), 3.83 (s, 1202, 730 603 21137 ’ 3H), 2.06 (s, 3H), 1.24 (d, J ' =61 Hz, 3H), 1.06 (d,J= 7.2 Hz, 3H). 191: NMR (376 MHz, CDC13) 8 -13420, —134.65. 1H NMR (400 MHz, CDC13) 8.27 (s, 1H), 8.23 (d,./: 7.9 Hz, 1H),7.11 4 6.99 (m, 5H), 6.93 (d, J: 5.3 Hz, 1H), 6.71 (dd, J: 12.0, 8.4 Hz, 2H), 5.74 4 5.65 (m, 3H), 4.55 (p, J: 7.2 Hz, 1H), 3.90 (s, 3H), 3.77 (s, 3H), 3.75 (s, 3H), 2.16 (s, HRMS-ESI (m 2) 3H), 2.14 (s, 3H), 2.06 (3, (Thin ?lm) ([M+H]+) 3H), 1.23 (d, J: 6.2 Hz, 3382, 2941, 3H), 0.97 (d, .1: 7.2 Hz, calcd for 518 1737, 1676, 3H). 4 C32H39N209, ‘ 11555; 172353” 50, found, 3’ 3 13C NMR ( 10] MH2’ 595.2645 CDC13) 6 , 170.22, 162.87, 160.26, 156.53, 156.36, 145.68, 143.94, 142.72, 133.75, 133.58, 130.48, 130.36, 126.81, 126.38, 126.10, 125.87, 110.06, 109.93, 109.49, 89.58, 73.66, 56.27, 56.16, 55.33, 55.30, 48.16, 20.85, 19.32, 1?.91, 16.33, 16.25.
[Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. n . :\1» \\\\\ ‘\‘\1 MP MASS NMR No, \'\'\ 13‘ (‘0 (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.25 (dd, .1: 6.5, 3.4 Hz, 2H), 7.07 (d, .1: 3.0 Hz, 1H), 6.92 (d, J: 5.4 Hz, 1H), 6.87 ((17: 31 Hz, 1H), 6.77 (d, .1: 8.8 Hz, 1H),6.71(d,J= 8.8 Hz, 1H), 6.66 (ddd, J: 11.1, 8.9, 3.0 Hz, 2H), 5.92 (dq, .1: 9.9, 6.1 Hz, 1H), 5.72 (d,J= 1.7 Hz, 2H), 4.94 (d, J: 10.0 Hz, 1H), 4.56 (p, .1: 7.2 Hz, HRMS-ESI (/77 Z) 1H), 3.89 (s, 3H), 3.81 (s, (Thin ?lm) ([M+H1+) 3H), 3.74 (s, 3H), 3.72 (s, 3381, 2939, calcd for 3H), 3.71 (s, 3H), 2.06 (s, 519 1737, 1676, C32H39NZOU: 3H), 1.25 (d, J: 6.3 Hz, 1498, 1233, 627.2548; found, 3H), 0.99 (d, J: 7.2 Hz, 1043, 729 627.2541 3H). 13CN1\4R(101 MHz, CDC13)6 172.39, 170.22, , 160.23, 153.47, 153.45,151.89,151.78, 145.68, 143.88, 142.78, 130.73, 130.69, 116.45, 115.38,112.14,112.13, 111.83,111.55,109.45, 89.59, 73.02, 56.34, 56.29, 56.15, 55.67, 5559,4817, 43.90,20.86,18.91, 17.97.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No, (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.26 (d, .1: 5.4 Hz, 1H), 8.23 (d, J: 7.8 Hz, 1H), 7.05 (d, J: 8.5 Hz, 1H), 6.98 (d, .1: 8.4 Hz, 1H), 6,93 (d, J: .4 Hz, 1H), 6.90 (d, .1: 2.7 Hz, 1H), 6.82 (d, J = 2.7 Hz, 1H), 6.63 (ddd, J: 18.1, 8.3, 2.7 Hz, 2H), 5.72 (d, .1: 1.6 Hz, 2H), 5.66 (dq, J: 10.0, 6.1 Hz, 1H), 4.56 (p, J: 7.3 . HRMS—ESI (m z) Hz, 1H), 4.46 (61,7: 10.1 ?“ min) ([M4H]+) Hz, 1H), 3.90 (s, 3H), 3.73 3382, 2937, 5 ,5, (s, 6H), 2.33 (s, 3H), 2.28 (s, ;, 1759, 1677,, calcd for 520 3H), 2.06 (s, 3H), 1.32 (d, .1q q 4 1500, 1455, C32H36N200, : 6 1 H ,H) 0 99 (d J: 1202, 1042, 595.2650; found, ' 7‘Z’2’H gm ’ 730 595.2652 ' ' [73C NMR (101 MHz, CDC13) 6 , 170.22, 162.89, 160.25, , 157.89, 145.69, 143.92, 142.66, 140.37, 139.85, 131.44,131.11,128.89, 128.62, 114.67, 113.64, 111.28,111.11, 109.52, 89.57, 74.55, 56.17, 55.19, 48.13, 47.87, 29.30, 20.86, 19.30, 1926,1888, 17.81.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No, (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.39 (d, .1: 7.1 Hz, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.44 (dd, J: 8.7, 5.0 Hz, 1H), 7.23 (dd, J: 8.7, 5.0 Hz, 1H), 7.1 1 (dd, .1: 9.0, 2.8 Hz, 1H), 7.07 (dd, J: 9.7, 2.8 Hz, 1H), 7.00 (d, J: 5.5 HRMS-ESI (/17 Z) Hz, 1H), 0.90 4 0.87 (m, (Thin ?lm) ([M+H]+) 2H), 5.00 (dq, J: 815, 0.2 Hz, 1H), 4.09 (d, J: 8.8 Hz, 1769, 1737, calcd for 521 1H), 4.02 (d, .7: 12.4 Hz, 1677, 1496, C31H35F2N208, 1H), 4.00 4 4.53 (m, 1H), 1195, 1174, 602.23 89, found, 4.50 (d, J: 12.0 Hz, 1H), 1095 60223 95 4.44 (d, .1: 12.5 Hz, 1H), 4.40 (d, J: 12.5 Hz, 1H), 3.90 (s, 3H), 3.43 (s, 3H), 3.38 (s, 3H), 2.39 (s, 3H), 1.28 (d, J: 0.2 Hz, 3H), 1.04 (d, J: 7.2 Hz, 3H). "’1? NMR (370 MHz, CDClg) —115.57, —115.90.
[Annotation] an None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS N1VJR No. (‘0 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.40 (d, .1: 6.4 Hz, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.45 (dd, J: 8.7, 5.6 Hz, 1H), 7.21 (dd, J: 8.7, 5.6 Hz, 1H), 7.17 4 7.05 (m, 2H), 7.00 (d, J: 5.5 Hz, 1H), 6.97 FIRMS-13810772) — 6.82 (m, 2H), 5.62 (dq, J: (Thin ?lm) +) 8.2, 6.2 Hz, 1H), 4.70 (d, .1: 3385, 2976, 8.7 Hz, 1H), 4.67 (d, J: 12.7 1770, 1738, calcd for 522 Hz, 1H), 4.62 — 4.50 (m, 1678, 1506, C33H39F2N2O8, 2H), 4.48 (d, J: 12.5 Hz, 1200, 1 175, 629.2669; found, 1H), 4.43 (d, J: 12.7 Hz, 1155, 1096 629.2666 1H), 3.90 (s, 3H), 3.62 — 3.45 (m, 4H), 2.39 (s, 3H), 1.30 4 1.25 (m, 6H), 1.23 (t, J: 7.0 Hz, 3H), 1.05 (d,J= 7.2 Hz, 3H). 19F NMR (376 MHz, CDC13) 415.69, 415.98. 1HNMR (400 MHz, CDC13) 8.41 (d, J: 6.8 Hz, 1H), 8.30 (d, .1: 5.4 Hz, 1H), 7.36 — 7.28 (m, 2H), 7.26 — 7.18 HRMS-ESI (m~"'z) (m, 2H), 7.18 — 7.10 (m, 2H), ([M+H]+) 6.97 (d, .1: 5.5 Hz, 1H), 6.67 _ 6.46 (m, 2H), 5.83 (dq, J: calcd for 523 9.9, 6.2 Hz, 1H), 4.62 — 4.46 C28H30FN2O7, (m, 2H), 3.87 (s, 3H), 3.82 525.203 7; found, (s, 3H), 2.38 (s, 3H), 1.23 (d, 525.2025 J: 6.2 Hz, 3H), 0.91 (d,J= 7.1 Hz, 3H). 19F NMR (376 MHz, CDC13) —113.24. ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No1 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.40 (d, .1: 7.9 Hz, 1H), 8.30 (d, J: 5.4 Hz, 1H), 7.35 — 7.17 (m, 5H), 7.17 - 7.08 HRMS-ESI (m z) (m, 1H), 6.97 (d, J: 5.5 Hz, ([M+H]+) 1H), 6.93 _ 6.79 (m, 2H), ,,HANK/5.; 5.77 (dq, J: 10.2, 6.1 Hz, calcd for 524 ;;'41/ 1H), 4.60 — 4.47 (m, 1H), C28H30FN2O6, .v2/. 4.28 (d, .1: 10.2 Hz, 1H), ,, 509.2088; found, 3.87 (s, 3H), 2.38 (s, 6H), 509.2083 1.26 (d, J: 6.1 Hz, 3H), 0.93 (d, .1: 7.2 Hz, 3H). 19F NMR (376 MHz, CDC13) -11666. 1H NMR (400 MHz, CDC13) 8.42 (d, .1: 8.1 Hz, 1H), 8.30 (d, .1: 5.6 Hz, 1H), 7.35 - 7.21 (m, 5H), 7.17 (ddt, J= 65,54, 18 Hz, 1H), 6.98 (d, HRMS-ESI (/17 Z) .1: 5.4 Hz, 1H), 6.58 (td, .1: ([M+H]+) 8.3, 2.6 Hz, 1H), 6.51 (dd, J calcd for = 10.9, 2.5 Hz, 1H), 5.81 CZXH30FNZO77 (dq,.]: 10.1,61 Hz, 1H), 525.203 7; found, 4.63 — 4.43 (m, 2H), 3.87 (s, 525.2035 3H), 3.75 (s, 3H), 2.38 (s, 3H), 2.15 (s, 3H), 0.99 (d, .1 : 7.1 Hz, 3H) 19F NMR (376 MHz, CDClg) -11359.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP MASS NMR No. (‘0 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.47 - 8.36 (m, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.35 (dd, J: 8.7, 5.7 Hz, 1H), 7.30 — 7.15 (m, 5H), 6.99 (d, .]= 5.5 HRMS-ESI (m Z) Hz, 1H), 6.85 (1d, .1: 8.4, ([M+H]+) 2.8 Hz, 1H), 6.79 (dd, J: 9.8, 2.8 Hz, 1H), 5.73 (dq, J calcd for 526 : 10.0, 6.1 Hz, 1H), 4.60 - C28H30FN2067 4.47 (m, 1H), 4.26 (d, .1: 509.2088; found, .0 Hz, 1H), 3.89 (s, 3H), 509.2079 2.38 (s, 3H), 2.30 (s, 3H), 123 (d, J: 6.1 Hz, 3H), 0.96 (d, J: 7.1 Hz, 3H).
"’F NMR (376 MHz, CDC13) lH NMR (400 MHz, CDCH) 8 8.41 (d, J: 5.0 Hz, 1H), 8.30 (d, J: 5.4 Hz, 1H), 7.23 — 7.19 (m, 2H), 7.19 — 7.10 (m, 1H), 7,03 (d, J: 7.9 Hz, SI (m/Z) 2H), 6.97 (d,.]= 5.5 Hz, ([1V1+H]+) 1H), 6.63 — 6.50 (m, 2H), calcd for 5.80 (dq,J: 9.6, 6.1 Hz, C29H32FN2O7, 1H), 4.61 — 4.46 (m, 2H), 539.2193; found, 3.88 (s, 3H), 3.81 (s, 3H), 539.2180 2.38 (s, 3H), 2.25 (s, 3H), 1.22 (d, J = 6.2 Hz, 3H), 0.95 (d, .1: 7.2 Hz, 3H). 19F NMR (3 76 MHz, CDC13) a —113.44_ [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No. (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.40 (d, .1: 8.6 Hz, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.28 (dd, J: 8.8, 5.9 Hz, 1H), 7.18 - 7.10 (m, 2H), 7.02 (d, HRMS-ESI (m Z) .1: 79 Hz, 2H), 6.98 (d, .1: ([M+H]+) 5.5 Hz, 1H), 6.92 — 6.78 (m, 2H), 5.74 (dq, J: 10.0, 6.1 calcd for 528 Hz, 1H), 4.62 _ 4.45 (m, 1H), C29H32FN2067 4.24 (d, J: 10.1 Hz, 1H), 523.2244; found, 3.88 (s, 3H), 2.38 (s, 3H), 2.37 (s, 3H), 2.24 (s, 3H), 1.24 (d, J: 6.1 Hz, 3H), 0.97 (d, J: 7.2 Hz, 3H).
"’F NMR (376 MHz, CDC13) -116.88.
'H NMR (400 MHz, CDCH) 8 8.41 (d, J: 7.9 Hz, 1H), 8,31 (d, J: 5.4 Hz, 1H), 7.37 —7.23 (m, 1H), 7.20 — 7.12 (m, 2H), 7,06 (d, J: 7.8 Hz, 2H), 6.98 (d,.]= 5.5 Hz, HRMS-ESI (m z) 1H), 6.57 (td, .1: 8.3, 2.5 ([M+H]+) Hz, 1H), 6,50 (dd, J: 11.0, calcd for 2.6 Hz, 1H), 5.78 (dq, J= C29H32FN2O7, 102,61 Hz, 1H), 4.69 — 4.41 539.2193; found, (m, 2H), 3189(5, 3H), 3.76 539.2182 (s, 3H), 2.38 (s, 3H), 2.27 (s, 3H), 1.21 (d, .1: 6,] Hz, 3H), 0.98 (d, .1: 7.1 Hz, "’1? NMR (376 MHz, CDClg) -113.82.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS NMR No. (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.40 (s, 1H), 8.30 (d,./: .4 Hz, 1H), 7,33 (dd, J: 8.7, 5.8 Hz, 1H), 7.20 — 7.04 (m, 4H), 6.98 (d, J: 5.5 Hz, 1H), 6.84 (td, .1: 8.5, 2.9 HRMS-ESI(I1IZ) Hz, 1H), 6.77 (dd, J: 9.6, ([M+H]+) 2.4 Hz, 1H), 5.71 (dq,J= calcd for 10.1, 6.1 Hz, 1H), 4.61 -445 C29H32FN206, (m, 1H), 4.21 (d, J: 10.1 523 .2244; found, Hz, 1H), 3.89 (s, 3H), 2.38 523 .2229 (s, 3H), 2.30 (s, 3H), 2.28 (s, 3H), 1.23 (d, J: 6.0 Hz, 3H), 0.96 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) -11733. 1H NMR (400 MHz, CDC13) 8.40 (d, .1: 6.0 Hz, 1H), 8.30 (d, .1: 5.5 Hz, 1H), 7.35 - 7.22 (m, 2H), 7.13 (dd, J: 8.3, 6.4 Hz, 1H), 6.99 (d,J= HRMS-ESI (m z) .5 Hz, 1H), 6.96 - 6.84 (m, 2H), 6.65 - 6.51 (m, 2H), calcd for 5.79 (dq, J: 9.7, 6.2 Hz, C28H29F2N207, 1H), 4.64 _ 4.47 (m, 2H), 543.1943; found, 3.88 (s, 3H), 3.81 (3,311), 36 2.38 (s, 3H), 1.23 (d, J: 6.1 Hz, 3H), 0.99 (d, .1: 7.2 Hz, 19F NMR (376 MHz, CDCl;) 4129241648.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by an Cmpd. 53:; MP IR NMR 3445s Nb‘ g 6C) (mn4) GH;BC,”F) ?iymy?3(40034Hz,cx)Ch) J:32Hz1HL 83lmw]:54fk,u?,729 :HMm3?6%@J= Hmnggonm 55H11HL6WL681mL QNHHT) 4Hl57IMqJ:lOL64 Hz, 1H), 4.60 — 4.49 (m, 1H), calcd for 532 y\ 426(d?l=10()Hz,H{) C28H20F2N2Oo, 4 ’3 ’3 a x ‘189(S*3FD’2J8(S’3H) 5271993'fbund 5271584 ’ 235(3,3HL J==62 ' Hz3HyLmu¢J=12Hz ”FrmuR4376hmHz(j)Ch) —H6oz—H638 ?iymy?3(40034Hz,cx)Ch) 58M(¢J:58HZIHL 8MM¢J:54H11HL7B -7l8(nL3}D,702-689 HMM$E$OHQ (m ??658a¢J=8425 QNH{H+) HLIPD,652(dd“/:109, 26I{;]}D,576(dq?l= cam for 533 10.0, 6.2 Hz, 1H), 4.60 — 4.46 C28H20F2NZO77 a ’3 a yBJWBAmmd OEZHl388§”H1375 (S, 3H), 2.38 (S, 3H), 1.21 (d, 543.1928 J=62HL3HLLW(¢J= 12HL3H) mFT?y?{(376h{Hz,C?)Ch) 3—H32@_H64L [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan CmNE.d. MP 1R NMR (0C) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.40 (d, .1: 8.1 Hz, 1H), 8.30 (d, J: 5.4 Hz, 1H), 7.33 (dd, J: 8.6, 5.7 Hz, 1H), 7.23 _ 7.13 (m, 2H), 7.04 _ HRMS-ESI(/11z) 6.92 (m, 3H), 6.86 (td, J: ([M+H]+) 8.5, 2.8 Hz, 1H), 6.80 (dd, J = 9.7, 2.8 Hz, 1H), 5.69 (dq, 534 .1: 9.9, 6.2 Hz, 1H), 4.63 — C) ‘jg 52281 93317 £61138 4.45 (m, 1H), 4.24 (d, J: 9.8 €27 11985 1 Hz, 1H), 3.89 (s, 3H), 2.38 1 ' (s, 3H), 2.28 (s, 3H), 1.23 (d, J: 6.1 Hz, 3H), 0.99 (d,J: 7.2 Hz, 3H).
”P NMR (376 MHz, CDC13) 8 —115.54, -116.80.
'H NMR (400 MHz, CDCH) 8.49 — 8.39 (m, 1H), 8.30 (d, J: 5.5 Hz, 1H), 7.19 — . - HRMS-ESI m z) 7.053H)? 5.78 (dq, J: 10.2,m, 6H 7.01 4 6.92 111161) ([M+H]+() , 6(.1m, 3385,2982, Hz, 1H), 4.59 — 4.46 (m, 535, 1771,1737,, calcdfor 1H) 396(d 1:102HZ 1679, 1605, C26H33N200, 505.233, 1H)1 3'86 (31m) 2137 (37 1508 found, 505.2333 1 1 1 1 ‘ 1 3H), 2.30 (s, 3H), 2.27 (s, 3H), 1.23 (d, .1: 6.2 Hz, 3H), 0.90 (d, J: 7.2 Hz, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan Cmpd.
MASS N1VJR No1 (cm ) (1H7 13c:1 19F) 1H NMR (400 MHz, CDC13) 8.41 (d, .1: 5.6 Hz, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7,23 (dd, J: 8.5, 6.6 Hz, 1H), 7.16 (dd, J: 8.6, 5.9 Hz, 1H), 6.99 (d, .1: 5.5 Hz, 1H), 6.81 (qd,J= 9.1, 8.3, HRMS-ESI (m/Z) 2.8 Hz, 2H), 6.57 (td, J= (Thin ?lm) ([M+H]+) 83,25 Hz, " 1H), 6.51 (dd, .1 ',cdyér.’ 3377, 2985, calcd for = 10.8, 25 Hz, 1H), 5.68 536 av 1771, 1736, 2:,tz, C29H31F2N2O7, (dq,J= 10.0, 6.1 Hz, 1H), ait. 1677, 1502, «7 557.2094; found, 4.74 (d, .1: 10.0 Hz, 1H), 557.2082 4.62 — 4.49 (m, 1H), 3.90 (s, 3H), 3.76 (s, 3H), 2.42 (s, 3H), 2.38 (s, 3H), 1.21 (d, .1 : 5.9 Hz, 3H), 1.04 (d,J: 7.2 Hz, 3H).
"’F NMR (376 MHz, CDC13) —113.52, —117.02.
'H NMR (400 MHz, CDCH) 8.40 (d,J= 6.1 Hz, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.31 (dd, .1: 8.4, 6.7 Hz, 1H), HRMS-ESI (m z) 7,23 — 7.14 (m, 1H), 6.99 (d, (Thin ?lm) ([M+H]+) J: 5.5 Hz, 1H), 6.84—6.68 3376, 2940, (m, 2H), 6.58 (td, .1: 83,25 calcd for 537 1770, 1737, Hz, 1H), 6.52 (dd, J: 10.8, F3NZO7: 1678, 1601, 2.5 Hz, 1H), 5.86 — 5.73 (m, 561.1843, found, 1502, 1 196 1H), 4.78 (d, .1: 9.9 Hz, 561 . 1836 1H), 4.65 4 4,43 (m, 1H), 3.90 (s, 3H), 3.75 (s, 3H), 2.38 (s, 3H), 1.24 (d, .1: 6.1 Hz, 3H), 1.04 (d, .1 : 7.2 Hz, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.44 4 8.37 (m, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.33 (dd, J: 8.5, 5.8 Hz, 1H), 7.04 (dd, .1: 8.4, 6.8 Hz, 1H), 6.99 (d, .1: 5.5 Hz, 1H), 6.88 — 6.74 (m, 2H), 6.64 — 6.53 (Thin ?lm) HREEEEJ" ‘) (m, 2H), 5.67 (dq, J: 9.8, “5378 2986 538 1770’ 1736’ calcd for 6.1 Hz, 1H), 4.74 (d, .1: 9.8 16777 15017 F2N207, HZ, 1H), 4.62 — 4.4501], 1196 ’ 557.2094, found, 1H), 3.90 (s, 3H), 3.84 (s, 7 557.2091 3H), 2.38 (s, 3H), 2.27 (s, 3H), 1.25 (d, J : 6.2 Hz, 3H), 0.98 (d, J: 7.2 Hz, 19F NMR (376 MHz, CDC13) —112.97, -11743. 1H NMR (400 MHz, CDC13) 8.43 — 8.35 (m, 1H), 8.31 (d, .1: 5.4 Hz, 1H), 7.33 (dd, SI (m/z) J= 8.6, 5.7 Hz, 1H), 7.19 — (Thin ?lm) ([M+H]+) 7.07 (m, 1H), 7.00 (d, J: 5.5 3377, 2983, Hz, 1H), 6.90 4 6.74 (m, calcd for 539 1771,1738, 4H), 5.68 (dq,./: 12.0, 6.1 C H PM) 1677, 1502, 54§81§g4? 1,6111% Hz, 1H), 4.62 (d, J = 9.9 Hz, 1201 5451896 ° 1H), 4.61 44.49 (m, 1H), ' 3.90 (s, 3H), 2.38 (s, 3H), 2.28 (s, 3H), 1.27 (d, J: 6.1 Hz, 3H), 1.00 (d, .1: 7.2 Hz, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No, (CC) (cm'l) (1H, 13C. 191:) 1H NMR (300 MHz, CDC13) 8.43 (d, .1: 8.0 Hz, 1H), 8.31 (d, .7: 5.4 Hz, 1H), 7.37 HRMS-ESI (m/Z) 4 7.21 (m, 5H), 7.24 4 7.14 (Thin ?lm) ([M+H]+) (m, 1H), 6,98 (d, J = 5.5 Hz, 3388,2985, 1H), 0.89 4 0.84 (m, 1H), calcd for 540 1771,1737, 0.79—0.72 (m, 1H), 5.904 C H“ FN7O 1079, 1572, 5092120382- 18301610 5.72 (m, 1H), 4.50 (dq, J = 1508,1452 ‘ 1 ’ 81,711 Hz, lH),4.4l (01,7: 509.2078 .0 Hz, 1H), 3.89 (s, 3H), 2.38 (s, 3H), 2.24 (s, 3H), 1.24 (01, .1: 0.2 Hz, 3H), 1.00 (d, J : 7.2 Hz, 3H). 1H NMR (400 MHz, CDCL.) 8,42 (d, J: 8.2 Hz, 1H), 8.31 (dd,J= 5.5, 1.2 Hz, 1H), 7.29 4 7.17 (m, 3H), 7.07 4 0.89 (m, 3H), 0.87 HRMS-ESI (m z) (dd, J: 8.0, 1.7 Hz, 1H), (Thin ?lm) 0.80 4 0.72 (m, 1H), 5.75 3378, 2984, calcd for (dq, .1: 9.7, 0.1 Hz, 1H), 1771, 1737, C28H29FZNZO6: 4.02 4 4.50 (m, 1H), 4.39 (d, 1679, 1509 527.1988, found, J: 9.8 Hz, 1H), 3.89 (s, 3H), 527. 1975 2.38 (s, 3H), 2.25 (s, 3H), 1.26—1.21(m,3H), 1.01 (d, J = 7.2 Hz, 3H).
”P NMR (370 MHz, CDC13) 4115.07, -118.89.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H. 13C. 191:) 1H NMR (400 MHz. CDC13) 8.48 4 8.36 (m. 1H). 8.29 (d. J: 5.6 Hz. 1H). 7.26 4 7.21 (m. 1H). 7.20 — 7.16 (m. 2H). 7.07 (d. .1: 7.9 Hz. 2H). 6.96 (d. .1: 5.5 Hz.
. HRMSESI!” Z) 1H). 6.84 (dd. J: 8.1. 1.9 (Thm ?lm) ([M+H] ) Hz 1H) 6 74 (dd J = 11 3 3390. 2984. 1 1 1 .1 1 1 calcd for 2.2 Hz. 542 $1772 1H). 5.83 , 5.75 (m.. 3:16787 15087 C29H32FN206, 1H). 4.63 — 4.50 (m, 1H). 141152 1 523.2239. found. 4.37 (d. J: 10.1 Hz. 1H). 1 3.86 (s. 3H). 2.37 (s. 3H). 2.27 (s. 3H). 2.22 (s, 3H). 1.24 (d. J: 6.1 Hz. 3H). 1.00 (d. .1: 7.2 Hz. 3H). 191: NMR (376 MHz. CDC13) -11902. 1H NMR (400 MHz. CDC13) 8.42 (d. J: 7.9 Hz. 1H). 8.31 (d. .1: 5.4 Hz. 1H). 7.24 (dd. J = 9.6. 5.7 Hz. 1H). 7.17 (t. J: 7.9 Hz. 1H). 6.99 (d. .1: 5.5 Hz. 1H). 6.88 4 (Thin ?lm) @5451??? 7) 6.82 (m. 3H). 6.75 (dd.J: 11.3. 2.2 Hz. 1H). 5.72 (dq.J 3384 2983 : 9.8. 6.1 Hz. 1H). 4.63 (d. .1 543 17721 17371 calcd for 16791 15911 C29H31F2N206. : 10.0 Hz. 1H). 4.62 4 4.51 15071 14521 541.2145. found. (m. 1H). 3.89 (s. 3H). 2.39 1 38 (3. 3H). 2.38 (s. 3H). 2.24 (s. 3H). 1.26 (d. J: 6.1 Hz. 3H). 1.05 (d. J: 7.2 Hz. 191: NMR (376 MHz. CDC13) —116.51.—118.10.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H. 13C. 191:) 1H NMR (400 MHz. CDC13) 8.45 4 8.39 (m. 1H). 8.31 , (61.7: 5.5 Hz. 1H). 7.324 . HRMS'ESIEW) 7.20 (m. 2H). 6.99 (d. J: 5.5 £1111“ ?lm) ([M+H] ) Hz, 1H). 6.88 4 6.84 (m. 17:11:39 calcd for 1H). 6.84 4 6.73 (m. 3H). 16787 15047 C28H23F3N206; 5.85 — 5.74-(111. 1H). 4.70 (d. 1453’ 14.321 545.1894; found. J: 9.9 Hz. 1H). 4.63 44.52 1 ‘ 545.1885 (m. 1H). 3.89 (s. 3H). 2.38 (s. 3H). 2.25 (s. 3H). 1.27 (d.
J: 6.1 Hz. 3H). 1.04 (d. J: 7.2 Hz. 3H). 1H NMR (500 MHZ. CDC13) 8.41 (s. 1H). 8.32 (d../: .5 Hz. 1H). 7.31 4 7.27 (m. 2H). 7.22 (t. J: 7.7 Hz. 2H). 7.17 (d. .1: 8.1 Hz. 2H). 7.15 4 7.10 (m. 1H). 7.09 (d. .1: 7.9 Hz. 2H). 6.99 (d. J: 5.5 . Hz. 1H). 5.79 (dq. J: 10.1. $172“ $191312) 6.1 Hz. 1H). 4.57 4 4.47 (m. 1770117347 1H). 4.01 (d.J= 10.1 Hz. 1675’ 1508’ ESIMS m z 4912 1H). 3.90 (s. 3H). 2.38 (s. 1451’ 1309’ ([M+H] ) 3H). 2.28 (s. 3H). 1.24 (d. .1 1 7 :62 Hz. 3H). 0.88 (d.J= 1200. 1174. 7 2 HZ 3H) 1046.907. ' 1 ' 802.730. 6 C NMR (126 MHz. 5172.24. 168.91. 162.24. . 146.64. 141.73. 141.57. 138.27. 137.43. 136.47. 129.44. 128.46. 127.99. 126.56. 109.68. 73.36. 57.53. 56.27. 47.83, 20.97. 20.75. 19.24. 17.92.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (500 MHz, CDC13) 8.42 (s, 1H), 8.32 (d,./: .4 Hz, 1H), 7.29 4 7.23 (m, 4H), 7.18 (td, J: 6,0, 2.8 Hz, 3H), 7.04 (d, J: 7.9 Hz, 2H), 6.99 (d, .1: 5.5 Hz, 1H), 5.79 (dq, J= 98,62 (Thin ?lm) Hz, 1H), 4.57 — 4.49 (m, 3381, 2982, 1H), 4.02 (d, .1: 9.9 Hz, 1770, 1734, 1H), 3.90 (s, 3H), 2.38 (s, g; 1675, 1507, ESHXSIZ’Hai‘)“ 3H), 2.25 (s, 3H), 1.23 (d, J 546 1435, 1309, : 6.2 Hz, 3H), 0.93 (d, .7: 1199, 1174, 7.2 Hz, 3H). 1045,907, 804, 729, 13C NMR (126 MHz, 699 CDC13) 5 172.23, 168.92, 162.25, 159.41, 146.64, 141.59, 138.34, 137.44, 136.15, 129.13, 128.72, , 127.99, 126.77, 10968, 73.38, 57.41, 56.28, 47.87, 20.94, 20.76, 19.25, 18.00, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \\ MP IR NMR No. (0C) (cm'l) (1H, 13C, 191:) 1H NMR (500 MHz, CDC13) 8.41 (s, 1H), 8.32 (01,7: .4 Hz, 1H), 7.23 (dd, J : 8.7, 5.3 Hz, 2H), 7.18 — 7.13 (m, 2H), 7.05 (d, J = 7.8 Hz, 2H), 7.01 i 0.93 (m, 3H), .74 (dq, J: 9.0, 02 Hz, 1H), 4.58 — 4.50 (m, 1H), (Thin ?lm) 4.01 (d, .1: 9.0 Hz, 1H), 3.90 3380, 2982, (s, 3H), 2,38 (s, 3H), 2.20 (s, 1770, 1735, 3H), 1.22 (d, J = 0.2 Hz, 1070, 1507, ESHXSAZ’Hz?fgl 3H), 0,94 (d, .1: 7.2 Hz, 547 1451, 1310, 3H). \ 1200, 1175, 1158,1047, 13C1\11\4R(1201\4Hz, 908, 810, CDC13) 5 , 108.91, 709, 729 102.20, 101.04 (d, J = 245.3 Hz), 159.43, 140.03, , 138.05, 137.45, 137.32(d,J=3.3 Hz), 130.34, 129.50 (d, J=7.8 Hz), 129.22, 127.94, 115.53 (d,J= 21.3 Hz), 109.70, 73.21, 50.51, 50.28, 47.85, .94, 20.75, 19.15, 17.99. ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H. 13C, 191:) 1H NMR (500 MHz, CDC13) 8.40 (s, 1H), 8.32 (d,./: .4 Hz, 1H), 7.33 4 7.23 (m, 6H), 7.23 — 7.17 (m, 1H), 6.99 (d, J: 5.5 Hz, 1H), 6.93 (t, .1 : 8.6 Hz, 2H), 5.76 (dq, J: 9.9, 6.2 Hz, 1H), 4.55 (p, J: 7.2 Hz, 1H), 4.05 (d, J: (Thin ?lm) 9.8 Hz, 1H), 3.90 (s, 3H), 3379, 2983, 2.38 (s, 3H), 1.23 (d, J: 6.2 1770, 1736, Hz, 3H), 0.97 (d, J: 7.2 Hz, 1676, 1509, 3H). 548 ESI??1\S4:HZ]:1)95 ~1 1452, 1310, 1201,1175, 13CN1\4R(1261V1Hz, 1046, 908, CDC13)6 172.17, , 817, 732, 162.28, 161.59 (d,J:245.0 700 Hz), 159.44, 146.64, 141.48, 141.04, 137.47, l37.16(d,J:3.4 Hz), 129.60 (d, J: 7.9 Hz), 128.84, 128.02, 127.02, 115.28 21.1 Hz), 109.74, 73.24, 57.00, 56.28, 47.83, 20.75, 19.22, 18.02.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP 1R NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (500 MHz, CDC13) 8.39 (s, 1H), 8.32 (61,]: .5 Hz, 1H), 7.28 i 7.21 (m, 2H), 7.14 (d, J: 8.2 Hz, 2H), 7.09 (d, J: 7.9 Hz, 2H), 6.99 (d, .1: 5.5 Hz, 1H), 6.95 — 6.89 (m, 2H), .74 (dq, J: 10.0, 6.2 Hz, . - 1H), 45844.50 (m, 1H), $3315“ 3191?; 4.00 (d, J: 10.0 Hz, 1H), 1;,70’ 173 5’ 3.90 (s, 3H), 2.38 (s, 3H), 1676’ 150‘7’ ESIMS m 2 509.1 2.29 (s, 3H), 1.23 (d, J: 6.1 549 1451’ 1436’ ([M+H]+) Hz, 3H), 0,97 (d, J : 71 Hz, 1310,1201, 153;” £28 13C NMR (126 MHz, 7’31 ’ 5172.18, 168.91, 162.27, 161.54 ((1, .1: 2451 Hz), 159.44, 146.63, 141.50, 138.06, 137.48 ((1, J = 3.6 Hz), 136.65, 129.49 (d, J: 8.3 Hz), 127.86, 115.24 (d, J: 21.3 Hz), 109.73, 73.30, 56.66, 56.28, 47.83, 20.98, 20.75, 19.22, 18.02, [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. \ MP 1R NMR No. (0C) (cm'l) (1H.1"C,19F) 1H NMR (400 MHz. CDC13) 8.39 (d. .1: 8.1 Hz. 1H). 8.32 (d. J: 5.5 Hz. 1H). 7.34 — 7.22 (m. 5H). 7.20 — 7.14 (m. 1H). 6.99 (d. J: 5.5 Hz. 1H). 6.85 4 6.74 (m. 2H). .80 (dtd, J: 9.9. 7.3. 6.7. .4 Hz. 1H). 4.55 (dt.J= 8.1.7.1 Hz. 1H).4.41 (d..]: $5“ $1221). .0 Hz. 1H). 3.90 (s. 3H). 238 (s. 3H). 1.27 (d. J: 6.1 ” 1 ’ HZ1 3H’ )1 0.92 d.]:7.2H 1770, 1737, Sl32 311‘)” Z” 1676. 1503. ‘ 550 ([M+H]+) 145211310”4 13CNMR (126 MHz ‘ 322* i512 CDC13)5172,13. 168.91. , 162.27. 162.03 (dd.J= 9077 731 168.8. 12.1 Hz). 160.964 159.14 (m). 159.43. 146.64. 141.50. 140.06. 137.46. 129.88 (dd.J= 9.6. 5.6 Hz). 128.60. 128.27. . 124.68 — 124.00 (m). 111.60 (dd. J: 21.3. 3.6 Hz). . 1045541033 (m). 72.51. 56.28. 49.35. 47.80. 20.75. 18.92. 17.92.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.40 (s, 1H), 8.32 (d,./: .5 Hz, 1H), 7.25 4 7.16 (m, 3H), 7.05 (d, J: 7.9 Hz, 2H), 6.99 (d, .1: 5.5 Hz, 1H), 6.84 4 6.73 (m, 2H), .77 (dtd, J: 9.5, 6.5, 5.2 Hz, 1H), 4.59 — 4.51 (m, (Thin ?lm) 1H), 4.38 (d, .1: 9.8 Hz, 3384, 2983, 1H), 3.90 (s, 3H), 2.38 (s, 1771, 1737, 3H), 2.26 (s, 3H), 1.25 (d, J 1677, 1502, ESHXSAZ’HZ?fm : 6.2 Hz, 3H), 0.96 (d, J : 551 1452, 1310, 72 Hz, 3H). 1201, 1175, 1148, 1049, 13C NMR (126 MHz, 966, 908, CDC13) 5 172.12, 168.92, 732 162.78 — 159.09 (111), 146.64, 141.53, 137.46, 136.96, 136.56, 129.88 ((1, J: 57 Hz), , 128.16, 124.64 ((1, J=15,0 Hz),111.52(d,J :208 Hz), 109.71, 104.49 — 103.84 (m), 72.59, 56.28, 48.90, 47.84, 20.96, 20.75, 18.92, 18.00.
[Annotation] Mel.Chan None set by an [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Cmpd. MP IR NMR No. (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.37 (d, .1: 6.0 Hz, 1H), 8.32 (d, J: 5.4 Hz, 1H), 7.28 — 7.18 (m, 3H), 7.00 (d, J: .5 Hz, 1H), 6.97 — 6.90 (m, 2H), 6.86 4 6.75 (m, 2H), .76 (dtd, J: 9.7, 6.5, 5.2 Hz, 1H), 4.62 — 4.48 (m, (Thin ?lm) 1H), 4.39 (d, .1: 9.8 Hz, 3384, 2985, 1H), 3.91 (s, 3H), 2.38 (s, 1770, 1737, , 3H), 1.26 (d, J = 6.1Hz, 1676, 1503, $104184th +5312 3H), 1,00 (d, .1: 7.2 Hz, 552 ([ 1 ) 1201, 1175, 3H). 1160, 1148, 966, 847, 13C NMR (126 MHz, 825, 811, CDC13) 5 172.05, 168.91, 732 163.09 — 159.02 (111), 146.63, 141.42, 137.50, 135.78, 12982 (d, J: 8.2 Hz), 124.23 (d,J= 11.3 Hz), 115.42 (d,J= 21.3 Hz), 111.98 4111.29(m), 109.77, 104.80 — 103.42 (m), 72.42, 56.30, 48.69, 47.81, 20.75, 18.93, 18.00.
[Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan Cmpd. MP IR NMR No, (CC) (cm'l) (1H, 13C, 191:) 1H NMR (400 MHz, CDC13) 8.41 (d, .1: 7.4 Hz, 1H), 8.31 (d, J: 5.4 Hz, 1H), 7.32 — 7.20 (m, 4H), 7.19 — 7.11 (m, 1H), 7.12 — 7.02 (m, 2H), HRMS—ESI (m z) 6.98 (d, .1: 5.5 Hz, 1H), 6.90 ([M+H]+) (dd, J = 9.6, 8.1 Hz, 1H), .76 (dq, J: 100, 6.2 Hz, calcd for 553 1H), 4.59—4.45 (m, 1H), C28H30FNZOO’ 3 99 3‘ (d J: 10 1 Hz 509.2088; found, y ', ’ 1H) 1 3.88 (s, 5H), 2.37 (s, 3H), 509 2074' 2.22 (d, .1: 2.0 Hz, 3H), 1.23 (d, J: 6.1 Hz, 3H), 0,90 (d, J = 7.2 Hz, 3H).
”P NMR (3 76 MHz, CDC13) —120. 17.
'H NMR (400 MHz, CDC13) 8.40 (s, 1H), 8.31 (d, J: .4 Hz, 1H), 7.32 - 7,23 (m, 1H), 7.11 — 7.01 (m, 2H), 6.99 (d, J: 5.5 Hz, 1H), 6.88 (t, J: 9.3 Hz, 1H), 6.58 (td, HRMS—ESI (m z) .I: 8.3, 2.5 Hz, 1H), 6.52 ([M+H]+) (dd, J 2 109, 2.5 Hz, 1H), .74 (dq, J: 10.1, 6.2 Hz, calcd for 554 1H), 4.55 (dq, .1: 8.1, 7.2 C)‘)H11F7N)O7 557 20399,T fdund HZ’ 1H)” 4‘46 (d’ J : [0'1 ‘557 21091 ’ Hz, 1H), 3.90 (s, 3H),3.77 ' (s, 3H), 2,38 (s, 3H), 2.21 (d, .1: 1.9 Hz, 3H), 1.20 (d, J: 6.1 Hz, 3H), 0.99 (d, J = 7.1 Hz, 3H), 191: NMR (3 76 MHz, CDC13) -113,46,-120,45.
. I\0. — Compound Number [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan Table 3. Biological Testing Rating Scale Rating Table for Fungal Pathogens Not Tested No Activity Observed in the Reported Assay Table 4. Biological Activity — PUCCRT and SEPTTR Disease Control in High and Low Volume Applications HV activity at 100 ppm LV activity at 121.5 g/H * SEPTTR>X< PUCCRT"< SEPTTR* ' 1DP* 3DC"< lDP* 3DC* 3DC"< CCCCCC AAACCCC BADCCCC AAAABAA DABCCCC _DAACCCC _AAACCCC _BAACCCC ADAACCCC_C 107 ABAACCCC 109 BDDBCCCC [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] an Unmarked set by Mel.Chan VC .mVDDDBA W mm C paWR T VCmm 111 A WWW:0PWT LWCC MWCCW mm 113 CC 114 .A mwnAABBA A HWCCCC-CCa?gmmWoT.C AB AA C/CC CC C CC/C 121 AA BB AA —A124 AABAAA C/CC/CCCCC CCCCC B D C 130 B BD AA C/CC C/CC ”‘B131135137 BC ADAAADBAC CCCCC C C A BA CC/CCCCCCCCAA CCCCCCCCBA 142 C C CC AA AA AA 145 CC CCCCC .CC BA 148 CC CC CC BA BA .BA AABBAAAA ation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan mmam.mVCC W. mm MSCCCCCConWT HR mm W TmWCCCC aC 49 LWBAVC MWBA 1 150 PCC QSAAAAAmydo“ HWAAAA 189 C C CCCCC CCC A B AABAA BAA [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan HV activity at 100 Rpm LV activity at 121.5 g/H "< SEPTTR* PUCCRT"< SEPTTR* [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan ionNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan WC paWR.mVBDBABCDAA W mm onWTmwnADDADCBAA LWCCCCCCCCCVC mmMWCCCCCCCCCW a mydo“ C T 333333333 00009999999 WBAAAACBAA 0090123456 BA CCCCCCCC HWCCCCCCCCCCCC AB CC AA CC/CC/CC CC 44444444444 00111111111 0090123456700 AABACABAAAA DBDDAD CC/CC/CCCCCCCCCCCCC AAABACABABBAB CCCCCCCCCCCCC DD CC 44 22 5/0 AAA AAA CCCCCCCCCCCCC/CC/CCC CC/CC/CC/CCCCCCCCCCCCC/CC/CCC CC/CCC BAD CCC [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan WC .mWDDD mm W CmR mSBBonWT VC aCHR WoT 700 WBB mmBAB,x. .WTCC.1*W mm 22 mSCCCCCC 44 LWCC HWCCCC 463 C C C C/ D D D B [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan mm W. mm W mm CpawR VC aCHR 5m 44 6/0 45 PCC .mAPCC CComWTmmCCCC .x./ MATAD éADnnD (0.VTHWADBB 55 00 01 CC CC CC CC DBB AAA AAB [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan ation] Mel.Chan Unmarked set by Mel.Chan VC W M W a CpaWR OFmm VCmm awnWT 503 HWCC .m*TCC LWAAAB —‘—‘510 C 51] C 512 mWCCCCCCCCCCC MWBBDDDDABABD HWDABDDDABADD C B D D CC DA DA DA CC AB AB AB —‘—‘—525 CC )] C CCCCCCCCCCC 532 C BDAAABBBBDAA C AA A BBAAAAAAAAAAA CC AA AB AA 540 C C CCC AAA BBB AAA [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan HV activity at 100 ppm LV activity at 121.5 g/H PUCCRT* SEPTTR* * SEPTTR* 54] C C C C A B A A 542 C C C C A B A A C C C C A A A A C C C C A A A A C C A C A C C C C A A A A C C C C A A A A C C C C A A A A *Cmpd. No. — Compound Number *PUCCRT * Wheat Brown Rust (Puccima lri/icma) *SEPTTR * Wheat Leaf Blotch (Zyvnriois'epz‘ariu trilici) *lDP — 1 Day tant *3DC , 3 Day Curative *g/H , Grams Pcr Hoctarc *ppm — Parts Per Million Table 5. Biological ty — Disease Control at 100 ppm ALTESO* CERCBE"< COLLLA* LEPTNO"< >>CUD>CU I>>>>>>>>> 50> >> >>>>>>>>>>> >>>>>>>>>>> ation] Mel.Chan None set by Mel.Chan [Annotation] an MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan ALTESO"< CERCBE’:< COLLLA* LEPTNO"< i>lii>>>|>>>A A A A A A A A A A >lA A A A >iA A A A A A mepd. No. , Compound Number CALTESO — Tomato Early Blight (Alfemaria solani) *CERCBE 7 Leaf Spot of Sugar Beets (Cercospom be?co/a) *COLLLA 7 Cucumber Anthracnoso (( YONG/()H‘IICZIH? Ingmar/71297) *LEPTNO — Wheat Glume Blotch (Lepfosphaeria nodomm) *lDP — 1 Day Protectant Table 6. Biological Activity — Disease Control at 100 ppm PYRIOR* RHYNSE>X< VENTTN* Cmpd. No. lDP* 92 C A C 139 A A A 140 A C A 141 A A A 142 A A A 145 A A A 146 A A A 148 A A A 150 A A A 167 A A C 171 A A C 174 A A B l76 A A A 199 A A C 204 A A C 464 A A A [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan ed set by Mel.Chan PYRIOR"< RHYNSE>X< VENTIN’:< Cmpd. No. 1DP"< 468 A A A 472 A A A 475 A A B 524 A A A 528 A A A 532 C A C *Cmpd. N0, 4 Compound Number *PYRIOR —‘ Rice Blast (Pyriczz/aria oryzae) *RHYNSE — Barley Scald (R173 ‘I7colsp0rizmz 's) iVENTIN 4 Apple Scab (WWW/'0 a/l's) ilDP — 1 Day Protectant Table 7. Biological Activity — Disease Control at 25 ppm PHAKPA* Cmpd. N0. lDP”< 3DC’1< 139 A B 140 B D 141 A B 142 A B 92 B B 145 A B 146 A B 148 A B 150 A A 158 A B l67 A B 169 A D 171 A B 173 B D 174 A B 175 B D 176 B B 199 A B 204 A B 207 B D 208 A B 209 A B [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by an [Annotation] Mel.Chan Unmarked set by Mel.Chan PHAKPA>X< Cmpd. NO. 1DP* 3DC* 210 A D 211 A B 212 B D 213 A B 464 A A 468 A B 472 A B 475 A B 493 D D 494 D D 495 B D 496 B D 497 D D 498 A B 499 B B 500 A B 501 B B 502 B D 503 A D 504 B D 505 D D 506 D D 507 D D 508 B D 509 D D 510 B D 511 D D 512 D D 513 D D 514 D D 515 D D 516 B D 517 B D 518 B D 519 D B 520 D D 521 B D 522 B D 523 A B [Annotation] Mel.Chan None set by Mel.Chan [Annotation] Mel.Chan MigrationNone set by Mel.Chan [Annotation] Mel.Chan Unmarked set by Mel.Chan PHAKPA* Cmpd. No. 1DP* 3DC* 524 A B 525 A B 526 A D 527 A B 528 A B 529 A B 530 A B 531 A B 532 A B 533 A B 534 A B 535 B D 536 A B 537 A B 538 B B 539 A B 540 A B 541 A B 542 B D 543 A B 544 A B 545 B D 546 A B 547 A B 548 A D 549 B D 550 A B 551 A B 552 A B 553 B D 554 B D *Cmpd. No. , Compound Number *PHAKPA , Asian Soybean Rust (Pha/copsom pac/7VW‘I71'ZI') *lDP — 1 Day tant *3DC , 3 Day Curative

Claims (3)

1. A compound which is chosen from Compound Number ure 1004849615 O CH3 H3C O O CH3 141 H N O O CH3 H3C O 142 O CH3 N O O CH3 O CH3 H3C O O CH3 149 H N O O CH3 O CH3 H3C O O F O CH3 O CH3 194 N N O O CH3 H3C O CH3 O Cl O CH3 206 N O CH3 O CH3 OH F O CH3 387 N O O CH3
2. A ition including at least one of the compounds of claim 1 and a phytologically acceptable carrier material.
3. The composition of claim 2 further comprising at least one of the compounds of claim 1 and r pesticide including fungicides, insecticides, nematocides, miticides, arthropodicides, bactericides and combinations thereof. 1004849615
NZ748767A 2015-12-18 Picolinamide compounds with fungicidal activity NZ748767B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462098120P 2014-12-30 2014-12-30
US201462098122P 2014-12-30 2014-12-30
NZ732641A NZ732641A (en) 2014-12-30 2015-12-18 Picolinamide compounds with fungicidal activity

Publications (2)

Publication Number Publication Date
NZ748767A NZ748767A (en) 2023-08-25
NZ748767B2 true NZ748767B2 (en) 2023-11-28

Family

ID=

Similar Documents

Publication Publication Date Title
US11284620B2 (en) Picolinamide compounds with fungicidal activity
AU2019231764B2 (en) Picolinamides as fungicides
AU2015374376A1 (en) Picolinamides with fungicidal activity
AU2015374377A1 (en) Picolinamide compounds with fungicidal activity
CN106164070A (en) There is the macro ring picolinamide compound of Fungicidally active
CN107205399A (en) It is used as the picolinamide of fungicide
CN106061256A (en) Macrocyclic pyridinamide compounds with fungicidal activity
WO2015100183A1 (en) Macrocyclic picolinamides as fungicides
CN106470983A (en) Big ring picolinamide as antifungal
AU2020279818B2 (en) Fungicidal aryl amidines
WO2017116939A1 (en) Macrocyclic picolinamides as fungicides
NZ748767B2 (en) Picolinamide compounds with fungicidal activity
WO2017116956A1 (en) Macrocyclic picolinamides as fungicides