NZ745259B2 - Substituted piperidine compound and use thereof - Google Patents
Substituted piperidine compound and use thereofInfo
- 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
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
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- A—HUMAN NECESSITIES
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- C07D211/18—Heterocyclic 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
- C07D211/20—Heterocyclic 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
- C07D211/24—Heterocyclic 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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- C07D211/36—Heterocyclic 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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- C07D211/36—Heterocyclic 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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- C07D213/04—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
- C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
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- 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
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- 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
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- 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
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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)
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
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 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NZ745259A NZ745259A (en) | 2025-03-28 |
| NZ745259B2 true NZ745259B2 (en) | 2025-07-01 |
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