IP Library › Granted Patent US 8,653,091
Granted Patent B2
US 8,653,091 · App. 12/594,364 · Granted Feb 18, 2014

Pyrid-2yl fused heterocyclic compounds, and compositions and uses thereof

Inventors: Zhi-Liang Wei (Foster City, CA); John Kincaid (San Francisco, CA); Michael G. Kelly (Thousand Oaks, CA); Donogh John Roger O'Mahony (San Mateo, CA); Carl Kaub (San Mateo, CA)
Assignee: Evotec AG
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Quick Facts
Patent No.
US 8,653,091
App. No.
12/594,364
Granted
Feb 18, 2014
Kind
B2
Abstract

Fused heterocyclic compounds are provided according to formula 1a or 1b: where R 1 , R 2 , and R 3 are as defined herein. Provided compounds and pharmaceutical compositions thereof are useful for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, cognitive disorders, anxiety, depression, and others.

Claims (43)

1. A compound according to formula 1a:

wherein

R 1 is cycloalkyl, cycloheteroalkyl, or heteroaryl unsubstituted or substituted with one or more R 4 groups;

R 2 is substituted or unsubstituted C 1 -C 6 alkyl or cycloalkyl;

R 3 is halo, substituted or unsubstituted C 1 -C 6 alkyl or cycloalkyl;

each R 4 is independently selected from the group consisting of H, alkyl, acyl, acylamino, alkylamino, alkythio, alkoxy, alkoxycarbonyl, alkylarylamino, arylalkyloxy, arylalkyloxy, amino, aryl, arylalkyl, sulfo, substituted sulfo, substituted sulfonyl, substituted sulfinyl, substituted sulfanyl, azido, carbamoyl, carboxyl, cyano, cycloalkyl, cycloheteroalkyl, dialkylamino, halo, heteroaryloxy, heteroaryl, heteroalkyl, hydroxy, nitro, and thiol;

or a pharmaceutically acceptable salt, solvate, prodrug, tautomer or isotopic variant thereof.

2. A compound according to claim 1 , wherein R 3 is Cl, F, Me, Et, i-Pr, or cyclopropyl.

3. An enantiomerically pure compound according to formula 2a or 2c:

wherein R 1 , R 2 and R 4 are as in claim 1 ; or a pharmaceutically acceptable salt, solvate, prodrug, tautomer or isotopic variant thereof.

4. A compound according to claim 3 , wherein R 1 is substituted or unsubstituted heteroaryl.

5. A compound according to claim 3 , wherein R 1 is substituted or unsubstituted bicycloalkyl, or bicycloheteroaryl.

6. A compound according to claim 3 , wherein R 1 is unsubstituted pyridyl or unsubstituted pyrimidinyl.

7. A compound according to claim 3 , wherein R 1 is selected from substituted or unsubstituted quinolinyl, isoquinolinyl, methylenedioxyphenyl, imidazopyridyl, benzoxazolyl, and indolyl.

8. A compound according to claim 3 , wherein R 1 is

and wherein subscript n′ is selected from 1-5 and each R 5 is independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted acyl, substituted or unsubstituted acylamino, substituted or unsubstituted alkylamino, substituted or unsubstituted alkythio, substituted or unsubstituted alkoxy, aryloxy, alkoxycarbonyl, substituted alkoxycarbonyl, substituted or unsubstituted alkylarylamino, arylalkyloxy, substituted arylalkyloxy, amino, aryl, substituted aryl, arylalkyl, sulfo, substituted sulfo, substituted sulfonyl, substituted sulfinyl, substituted sulfanyl, azido, substituted or unsubstituted carbamoyl, carboxyl, cyano, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloheteroalkyl, substituted or unsubstituted dialkylamino, halo, heteroaryloxy, substituted or unsubstituted heteroaryl, substituted or unsubstituted heteroalkyl, hydroxy, nitro, and thiol.

9. A compound according to claim 8 , wherein subscript n′ is 1 or 2.

10. A compound according to claim 8 , wherein each R 5 is independently selected from H, Me, Et, Pr, iso-Pr, Ph, Cl, F, Br, CN, OH, OMe, OEt, OPh, COPh, CO 2 Me, CH 2 —N-morpholino, CH 2 —N-(4-Me-piperidino), NH 2 , CONH 2 , CF 3 , CHF 2 , OCF 3 , OCHF 2 , t-Bu, SMe, CH═CH—CO 2 H, SOMe, SO 2 Me, SO 2 CF 3 , SO 2 NH 2 , SO 3 H, SO 3 Me, cyclopropyl, triazolyl, morpholinyl, and pyridyl; and the subscript n′ is 1 or 2.

11. A compound according to claim 1 , wherein the compound is according to formula 3b, 3c, 3e, or 3f:

and wherein R 2 is as in claim 1 ; and each R 5 is independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted acyl, substituted or unsubstituted acylamino, substituted or unsubstituted alkylamino, substituted or unsubstituted alkythio, substituted or unsubstituted alkoxy, aryloxy, alkoxycarbonyl, substituted alkoxycarbonyl, substituted or unsubstituted alkylarylamino, arylalkyloxy, substituted arylalkyloxy, amino, aryl, substituted aryl, arylalkyl, sulfo, substituted sulfo, substituted sulfonyl, substituted sulfinyl, substituted sulfanyl, azido, substituted or unsubstituted carbamoyl, carboxyl, cyano, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloheteroalkyl, substituted or unsubstituted dialkylamino, halo, heteroaryloxy, substituted or unsubstituted heteroaryl, substituted or unsubstituted heteroalkyl, hydroxy, nitro, and thiol.

12. A compound according to claim 11 , wherein each R 5 is independently selected from H, Me, Et, Pr, iso-Pr, Ph, Cl, F, CN, OH, OMe, OEt, OPh, CF 3 , CHF 2 , OCF 3 , OCHF 2 , t-Bu, SO 2 Me, SO 2 CF 3 , and SO 3 Me.

13. A compound according to claim 11 , wherein R 5 is H, Cl, F, Me, CF 3 , SO 2 Me, or OMe.

14. A compound according to claim 11 , wherein R 2 is selected from Me, Et, n-Pr, t-Bu, CF 3 , CH 2 OH, CH 2 CH 2 OH, CH 2 CH 2 OAc, CH 2 (CH 2 ) 2 OH, CH 2 CH 2 NHMe, CH 2 NMe 2 , CH 2 CH 2 NMe 2 , CH 2 CONH 2 , CH 2 CONMe 2 , CH 2 COOH, CH 2 CH 2 COOH, CH 2 (CH 2 ) 2 COOH, CH 2 OMe, and CH 2 CH 2 OMe.

15. A compound according to claim 11 , wherein R 2 is selected from CH 2 NR 2 ′R 2 ″, CH 2 CH 2 NR 2 ′R 2 ″, and CH 2 CH 2 CH 2 NR 2 ′R 2 ″; and wherein R 2 ′ and R 2 ″ can join together to form a heterocyclic ring.

16. A compound according to claim 11 , wherein R 2 is selected from cyclopropyl, cyclobutyl or cyclohexyl.

17. A compound according to claim 11 , wherein R 2 is Me.

18. A compound according to claim 11 , wherein R 2 is Me, CH 2 OH or CH 2 CH 2 OH.

19. A compound according to claim 1 , selected from the group consisting of:

[6-(5-Methyl-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yl]-[(R)-1-6-trifluoromethyl-pyridin-3-yl)-ethyl]-amine;

[6-(5-Chloro-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yl]-[(R)-1-6-trifluoromethyl-pyridin-3-yl)-ethyl]-amine;

[6-(5-Chloro-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yl]-[(R)-cyclopropyl-(6-trifluoromethyl-pyridin-3-yl)-methyl]-amine;

(R)-3-[6-(5-Chloro-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-ylamino]-3-(6-methoxy-pyridin-3-yl)-propan-1-ol;

(R)-3-(6-Methoxy-pyridin-3-yl)-3-[6-(5-methyl-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-ylamino]-propan-1-ol;

(S)-2-[6-(5-Chloro-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-ylamino]-2-(6-methoxy-pyridin-3-yl)-ethanol;

(S)-2-(6-Methoxy-pyridin-3-yl)-2-[6-(5-methyl-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-ylamino]-ethanol;

(R)-3-(6-Methyl-pyridin-3-yl)-3-[6-(5-methyl-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-ylamino]-propan-1-ol;

(R)-3-[6-(5-Methyl-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-ylamino]-3-(6-trifluoromethyl-pyridin-3-yl)-propan-1-ol; and

[6-(5-Methyl-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yl]-[(R)-1-(2-methyl-pyrimidin-5 -yl)-ethyl]-amine;

or a pharmaceutically acceptable salt, solvate, prodrug, stereoisomer, tautomer or isotopic variant thereof.

20. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a pharmaceutically effective amount of a compound of claim 1 .

21. The pharmaceutical composition of claim 20 , wherein the carrier is suitable for parenteral administration.

22. The pharmaceutical composition of claim 20 , wherein the carrier is suitable for oral administration.

23. The pharmaceutical composition of claim 20 , wherein the carrier is suitable for topical administration.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 6, 2011
From: RENOVIS, INC.
To: EVOTEC AG
Reel/Frame 026450/0639 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 29, 2010
From: WEI, ZHI-LIANG; KINCAID, JOHN; KELLY, MICHAEL G.; O'MAHONY, DONOGH JOHN ROGER; KAUB, CARL
To: RENOVIS, INC.
Reel/Frame 024156/0558 →
Continuity (3)
Provisional Application 60921604 · Apr 2, 2007
Provisional Application 60921603 · Apr 2, 2007
Related Publication 20110009432A1 · Jan 13, 2011