Pyrrolidine orexin receptor agonists
The present invention is directed to pyrrolidine compounds which are agonists of orexin receptors. The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which orexin receptors are involved.
1. A compound of the formula I:
wherein:
X is —O— or —NH—, or X may be a direct bond to R 1 ;
Y is N or CH;
R 1 is selected from:
(1) -C 1-6 alkyl, where the alkyl is unsubstituted or substituted with one to six substituents independently selected from R 4 , and
(2) -C 3-6 cycloalkyl, where the cycloalkyl is unsubstituted or substituted with one to six substituents independently selected from R 4 ;
R 2 is selected from:
(1) hydrogen,
(2) -C 1-6 alkyl, where the alkyl is unsubstituted or substituted with one to six substituents independently selected from R 4 ,
(3) -C 3-6 cycloalkyl, where the cycloalkyl is unsubstituted or substituted with one to six substituents independently selected from R 4 ,
(4) -phenyl, where the phenyl is unsubstituted or substituted with one to three substituents independently selected from R 4 , and
(5) -heteroaryl, where the heteroaryl is selected from: pyridyl, pyrimidinyl, and pyrazinyl, and the heteroaryl is unsubstituted or substituted with one to three substituents independently selected from R 4 ;
R 2a and R 2b are independently selected from:
(1) hydrogen,
(2) hydroxyl,
(3) halogen, and
(4) -C 1-6 alkyl, where the alkyl is unsubstituted or substituted with one to six substituents independently selected from halogen;
R 3 is phenyl, where the phenyl is unsubstituted or substituted with one to three substituents independently selected from R 4 ,
R 4 is selected from:
(1) hydroxyl,
(2) halogen,
(3) C 1-6 alkyl, which is unsubstituted or substituted with one to six fluoro,
(4) -C 3-6 cycloalkyl,
(5) —O-C 1-6 alkyl,
(6) —O (C═O)-C 1-6 alkyl,
(7) —NH 2 ,
(8) —NH-C 1-6 alkyl,
(9) —NO 2 ,
(10) phenyl,
(11) —CO 2 H, and
(12) —CN;
or a pharmaceutically acceptable salt thereof.
2. The compound of claim 1 or a pharmaceutically acceptable salt thereof wherein X is —O—.
3. The compound of claim 1 or a pharmaceutically acceptable salt thereof wherein R 1 is selected from:
(1) methyl,
(2) ethyl,
(3) —CH 2 OH,
(4) —CH 2 CF 3 ,
(5) —CH 2 CHF 2 ,
(6) —CH(CH 3 ) 2 ,
(7) —CH 2 CH 2 CH 2 F,
(8) cyclopropyl,
(9) —CH 2 -cyclopropyl,
(10) —CH 2 -cyclobutyl, and
(11) —CH 2 O(C═O)CH 3 .
4. The compound of claim 1 or a pharmaceutically acceptable salt thereof wherein R 2 is selected from:
(1) hydrogen,
(2) —CH 2 (CH 3 ) 2 ,
(3) —CF 3 ,
(4) —CH 2 CHF 2 ,
(5) —CH 2 CF 3 , and
(6) phenyl, which is unsubstituted or substituted with —CF 3 or —CH 2 CF 3 .
5. A compound which is selected from: methyl 2-(((4-phenylcyclohexyl)oxy)methyl)-3-(phenylsulfonamido)pyrrolidine-1-carboxylate; methyl (CIS)-2-((((CIS)-4-phenylcyclohexyl)oxy)methyl)-3-(phenylsulfonamido)pyrrolidine-1-carboxylate; or a pharmaceutically acceptable salt thereof.
6. A pharmaceutical composition which comprises an inert carrier and a compound of claim 1 or a pharmaceutically acceptable salt thereof.