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NZ745259B2 - Substituted piperidine compound and use thereof - Google Patents
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NZ745259B2 - Substituted piperidine compound and use thereof - Google Patents

Substituted piperidine compound and use thereof

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Publication number
NZ745259B2
NZ745259B2 NZ745259A NZ74525917A NZ745259B2 NZ 745259 B2 NZ745259 B2 NZ 745259B2 NZ 745259 A NZ745259 A NZ 745259A NZ 74525917 A NZ74525917 A NZ 74525917A NZ 745259 B2 NZ745259 B2 NZ 745259B2
Authority
NZ
New Zealand
Prior art keywords
group
alkyl
optionally substituted
carbonyl
hypersomnia
Prior art date
Application number
NZ745259A
Other versions
NZ745259A (en
Inventor
Tatsuhiko Fujimoto
Koichiro Fukuda
Mariko HIROZANE
Takahiro Matsumoto
Kentaro Rikimaru
Hiromichi Sugimoto
Norihito Tokunaga
Original Assignee
Takeda Pharmaceutical Company Limited
Filing date
Publication date
Application filed by Takeda Pharmaceutical Company Limited filed Critical Takeda Pharmaceutical Company Limited
Priority claimed from PCT/JP2017/003610 external-priority patent/WO2017135306A1/en
Publication of NZ745259A publication Critical patent/NZ745259A/en
Publication of NZ745259B2 publication Critical patent/NZ745259B2/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P23/00Anaesthetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/48Drugs for disorders of the endocrine system of the pancreatic hormones
    • A61P5/50Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
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    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/20Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
    • C07D211/24Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by sulfur atoms to which a second hetero atom is attached
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    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
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    • C07D213/04Heterocyclic 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
    • C07D213/24Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms
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    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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
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    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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
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    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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
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    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
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Abstract

Provided is a substituted piperidine compound having an orexin type 2 receptor agonist activity. A compound represented by the formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof has an orexin type 2 receptor agonist activity, and is useful as a prophylactic or therapeutic agent for narcolepsy.

Claims (22)

Claims
1.
2. A compound represented by the formula: wherein R1 is (1) a hydrogen atom, (2) a C1-6 alkyl-carbonyl group optionally substituted by 1 to 7 substituents 10 selected from (i) a halogen atom, (ii) a cyano group, (iii) a hydroxy group, (iv) a C3-10 cycloalkyl group, (v) a C1-6 alkoxy group, (vi) a C6-14 aryl group, (vii) a C6-14 aryloxy group, (viii) a pyrazolyl group, a thiazolyl group, a pyrimidinyl group or a pyridazinyl group, each of which is ally substituted by an 15 oxo group, (ix) a pyrazolyloxy group optionally substituted by 1 to 3 C1-6 alkyl groups, (x) a C1-6 alkyl-carbonyl group, (xi) a C1-6 alkoxy-carbonyl group, (xii) a C1-6 alkyl-carbonyloxy group, (xiii) a C1-6 ulfonyl group, (xiv) a mono- or di-C1-6 alkylamino group, (xv) a C1-6 alkyl-carbonylamino group and (xvi) a (C1-6 (C1-6 alkyl-carbonyl)amino group, 20 (3) a C3-10 cycloalkyl-carbonyl group optionally substituted by 1 to 3 substituents selected from a halogen atom, a cyano group, a hydroxy group, an oxo group and a C1-6 alkyl group, (4) a C1-6 alkoxy-carbonyl group optionally substituted by 1 to 6 substituents selected from ium, a halogen atom and a C6-14 aryl group, 25 (5) a C3-10 lkyloxy-carbonyl group optionally substituted by 1 to 3 substituents selected from a C1-6 alkyl group, (6) a C6-14 aryl-carbonyl group optionally substituted by 1 to 3 substituents selected from a halogen atom and a C6-14 aryl group, (7) a C6-14 aryloxy-carbonyl group, (8) a furylcarbonyl group, a thienylcarbonyl group, a pyrazolylcarbonyl group, an olylcarbonyl group or a pyridylcarbonyl group, each of 5 which is optionally substituted by 1 to 3 tuents selected from a C1-6 alkyl group, (9) an azetidinylcarbonyl group, an oxetanylcarbonyl group, a pyrrolidinylcarbonyl group, a tetrahydrofuranylcarbonyl group, a tetrahydropyranylcarbonyl group or a morpholinylcarbonyl group, each of 10 which is optionally substituted by 1 to 3 substituents selected from an oxo group, a C1-6 alkyl-carbonyl group, a C1-6 alkoxy-carbonyl group and a C1-6 alkylsulfonyl group, (10) a mono- or di-C1-6 alkyl-carbamoyl group optionally substituted by 1 to 3 substituents selected from a halogen atom, a cyano group, a hydroxy group 15 and a C1-6 alkoxy group, (11) a mono- or di-C3-10 cycloalkyl-carbamoyl group, (12) a mono- or di-C6-14 aryl-carbamoyl group, (13) a C1-6 alkylsulfonyl group, (14) a C3-10 cycloalkylsulfonyl group, 20 (15) a C6-14 lfonyl group ally tuted by 1 to 3 halogen atoms, (16) a thienylsulfonyl group, a pyrazolylsulfonyl group, an imidazolylsulfonyl group, a pyridylsulfonyl group or a dihydrochromenylsulfonyl group, each of which is optionally substituted by 1 to 3 substituents selected from a C1-6 alkyl group, 25 (17) a mono- or di-C1-6 sulfamoyl group or (18) a C1-6 alkyl-carbonyl-carbonyl group; R2 is a C3-6 cycloalkyl group, a pyrrolidinyl group, a piperidinyl group or a dioxanyl group, each of which is ally substituted by 1 to 3 substituents selected from (1) deuterium, 30 (2) a halogen atom, (3) a hydroxy group, (4) a C1-6 alkyl group optionally substituted by 1 to 3 substituents selected from a halogen atom and a C6-14 aryl group, (5) a C3-10 cycloalkyl group, (6) a C1-6 alkoxy group ally substituted by a C3-10 cycloalkyl group, (7) a C6-14 aryl group optionally substituted by 1 to 3 substituents selected from a halogen atom, a cyano group, a C1-6 alkyl group optionally substituted by 1 to 3 halogen atoms, a C1-6 alkoxy group optionally tuted by 1 to 3 5 halogen atoms and a hydroxy group, (8) a C6-14 aryloxy group, (9) a tri-C1-6 ilyloxy group, (10) a pyrazolyl group, a thiazolyl group, a pyridyl group, a pyrimidinyl group, a quinazolinyl group, a benzothiazolyl group or an isoquinolinyl 10 group, each of which is optionally substituted by 1 to 3 substituents selected from a halogen atom, a C1-6 alkyl group and a C1-6 alkoxy group, and (11) a C6-14 aryl-carbonyl group; and R3 is a C1-6 alkyl group, or a mono- or di-C1-6 alkylamino group, or a salt thereof. 15 2. The compound according to claim 1, which is represented by the formula: wherein R1, R2 and R3 are as defined in claim 1, or a salt thereof.
3. The compound according to claim 1, wherein R1 is 20 (1) a hydrogen atom, (2) a C1-6 alkyl-carbonyl group optionally substituted by a y group, (3) a cyclopropanecarbonyl group, (4) a C1-6 alkoxy-carbonyl group or (5) a mono- or di-C1-6 alkyl-carbamoyl group; 25 R2 is (A) a exyl group optionally substituted by 1 to 3 substituents selected (1) a C1-6 alkyl group and (2) a phenyl group optionally substituted by 1 to 3 substituents selected from a halogen atom, a C1-6 alkyl group optionally substituted by 1 5 to 3 halogen atoms and a C1-6 alkoxy group or (B) a piperidinyl group optionally substituted by 1 to 3 pyrimidinyl groups; R3 is a C1-6 alkyl group or a di-C1-6 alkylamino group, or a salt thereof.
4. The compound ing to claim 1, wherein 10 R1 is (1) a C1-6 alkyl-carbonyl group optionally tuted by a hydroxy group, (2) a C1-6 alkoxy-carbonyl group or (3) a mono- or di-C1-6 alkyl-carbamoyl group; R2 is a cyclohexyl group optionally substituted by 1 to 3 substituents selected from 15 (1) a C1-6 alkyl group and (2) a phenyl group optionally substituted by 1 to 3 halogen atoms; and R3 is a C1-6 alkyl group, or a salt thereof.
5. The compound of claim 1, which is Methyl (2R,3S)((methylsulfonyl)amino) (((cisphenylcyclohexyl)oxy)methyl)piperidinecarboxylate or a salt thereof. 20
6. The compound of claim 1, which is N-((2R,3S)glycoloyl(((cis(2,3,6- orophenyl)cyclohexyl)oxy)methyl)piperidinyl)methanesulfonamide or a salt thereof.
7. The compound of claim 1, which is (2R,3S)-N-ethyl(((cis isopropylcyclohexyl)oxy)methyl)((methylsulfonyl)amino)piperidinecarboxamide or a salt f. 25
8. A medicament comprising the compound or salt according to any one of claims 1 to 7.
9. The medicament of claim 8, for use in therapy.
10. The medicament of claim 9, wherein the therapy ses treatment of a disease or disorder associated with an orexin type 2 or.
11. The medicament of claim 10, wherein the disease or disorder is selected from the 30 group consisting of narcolepsy, idiopathic hypersomnia, hypersomnia, sleep apnea me, narcolepsy syndrome accompanied by narcolepsy-like ms, omnia syndrome accompanied by daytime hypersomnia, Alzheimer’s, obesity, insulin resistance syndrome, cardiac failure, diseases related to bone loss, sepsis, disturbance of consciousness such as coma and the like, and side s and complications due to anesthesia, or for use as an etic nist.
12. The medicament of claim 10, wherein the disease or disorder is selected from the group consisting of narcolepsy, idiopathic hypersomnia, hypersomnia, or sleep apnea 5 syndrome.
13. The medicament of claim 10, wherein the disease or disorder is narcolepsy.
14. The compound or salt according to any one of claims 1 to 7 for use in therapy.
15. The compound or salt of claim 14, wherein the therapy ses treatment of a disease or disorder associated with an orexin type 2 receptor. 10
16. The compound of claim 15 or a salt thereof, wherein the disease or disorder is selected from the group consisting of narcolepsy, idiopathic hypersomnia, hypersomnia, sleep apnea syndrome, epsy syndrome accompanied by narcolepsy-like symptoms, hypersomnia syndrome accompanied by daytime hypersomnia, Alzheimer, obesity, insulin resistance syndrome, cardiac failure, diseases related to bone loss, sepsis, disturbance of consciousness 15 such as coma and the like, side effects and complications due to anesthesia, and anesthetic antagonist.
17. The nd of claim 15, or a salt thereof, wherein the disease or disorder is selected from the group consisting of narcolepsy, idiopathic hypersomnia, omnia, or sleep apnea syndrome. 20
18. The compound of claim 15, or a salt thereof, wherein the disease or disorder is narcolepsy.
19. Use of the compound or salt according to any one of claims 1 to 7 in the manufacture of a medicament for the treatment of a disease or er associated with an orexin type 2 receptor, n the disease or disorder is selected from the group consisting of narcolepsy, 25 idiopathic hypersomnia, hypersomnia, sleep apnea me, epsy syndrome accompanied by narcolepsy-like symptoms, hypersomnia syndrome accompanied by daytime hypersomnia, Alzheimer, obesity, insulin ance syndrome, cardiac failure, diseases related to bone loss, sepsis, disturbance of consciousness such as coma and the like, side effects and complications due to anesthesia, and anesthetic antagonist. 30
20. The use of claim 19, wherein the disease or disorder is selected from the group ting of narcolepsy, idiopathic hypersomnia, hypersomnia, sleep apnea syndrome, or side effects and complications due to anesthesia.
21. The use of claim 19, wherein the disease or disorder is narcolepsy.
22. The compound of claim 1, substantially as herein described with nce to any one of the examples and/or
NZ745259A 2017-02-01 Substituted piperidine compound and use thereof NZ745259B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2016019834 2016-02-04
PCT/JP2017/003610 WO2017135306A1 (en) 2016-02-04 2017-02-01 Substituted piperidine compound and use thereof

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NZ745259B2 true NZ745259B2 (en) 2025-07-01

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