Octahydropentalene compounds as chemokine receptor antagonists
View Patent ↗The present invention is directed to novel compounds of Formula (I) pharmaceutically acceptable salts thereof, pro-drugs thereof, biologically active metabolites thereof, isomers thereof or stereoisomers thereof wherein the variables are as defined herein. The compounds of Formula (I) are useful as chemokine receptor antagonists and as such would be useful in treating certain conditions and diseases, especially inflammatory conditions and diseases and proliferative disorders and conditions, for example, rheumatoid arthritis, osteoarthritis, multiple sclerosis and asthma.
1. A compound of Formula (I)
pharmaceutically acceptable salts, isomers thereof or stereoisomers thereof wherein
R a is H or optionally substituted (C 1 -C 6 )alkyl;
R b is selected from the optionally substituted group consisting of —(CH 2 ) n -aryl, —CH(CH 3 )-aryl, —(CH 2 ) n -aryl-aryl, —(CH 2 ) n -aryl-heteroaryl, —(CH 2 ) n —(C 3 -C 8 )cycloalkyl, —(CH 2 ) n -heteroaryl, —(CH 2 ) n -heterocyclyl and —(C 3 -C 8 )cycloalkyl-aryl; or
R a and R b are taken together with the nitrogen to form 2,3-dihydro-1H-isoindolyl, decahydroisoquinolinyl, optionally substituted piperidinyl or optionally substituted pyrrolidinyl;
Y is selected from the optionally substituted group consisting of 5,6,7,8-tetrahydro[1,6]naphthridinyl, —NH—(CH 2 ) n -heterocyclyl wherein the NH is attached to the carbonyl and -heterocyclyl-aryl wherein the heterocyclyl is attached to the carbonyl; and
n is 0, 1 or 2.
2. The compound or salt according to claim 1 wherein Y is selected from the optionally substituted group consisting of 5,6,7,8-tetrahydro[1,6]naphthridinyl, —NH—(CH 2 ) 2 -pyrrolidinyl and -piperazinyl-phenyl.
3. The compound or salt according to claim 2 wherein R a is H or methyl.
4. The compound or salt according to claim 3 wherein R b is selected from the optionally substituted group consisting of —CH 2 -phenyl, —CH 2 -phenyl-phenyl, —(CH 2 ) 2 -phenyl, —CH(CH 3 )-phenyl, —CH 2 CH 2 -phenyl-phenyl, —CH 2 -phenyl-pyrazolyl, phenyl-pyrazolyl, indanyl, —(CH 2 ) 2 -indolyl, 1,2,3,4-tetrahydronaphthyl, —(CH 2 )-pyrazinyl, —(CH 2 )-pyridinyl, —(CH 2 ) 2 -pyridinyl, —(CH 2 ) 2 -pyrrolidinyl, —(CH 2 ) 2 -thienyl, tetrahydrothienyl-1,1-dioxide, —(CH 2 ) 2 -piperidinyl, tetrahydropyranyl and -cyclohexyl-phenyl.
5. The compound or salt according to claim 4 wherein R b is selected from the optionally substituted group consisting of —CH 2 -phenyl, —(CH 2 ) 2 -phenyl, —CH 2 -phenyl-pyrazolyl, indanyl, —(CH 2 )-indolyl, 1,2,3,4-tetrahydronaphthyl, —(CH 2 ) 2 -pyridinyl and -cyclohexyl-phenyl.
6. The compound or salt according to claim 5 wherein Y is selected from the optionally substituted group consisting of 5,6,7,8-tetrahydro[1,6]naphthyridinyl and -piperazinyl-phenyl.
7. The compound or salt according to claim 6 wherein R b is selected from the optionally substituted group consisting of —CH 2 -phenyl, —(CH 2 ) 2 -phenyl, 1,2,3,4-tetrahydronaphthyl, —CH 2 -phenyl-pyrazolyl, indanyl, —(CH 2 ) 2 -pyridinyl and -cyclohexyl-phenyl.
8. The compound or salt according to claim 7 wherein R b is selected from the optionally substituted group consisting of —CH 2 -phenyl, 1,2,3,4 tetrahydronaphthyl and -cyclohexyl-phenyl.
9. The compound or salt according to claim 8 wherein R b is optionally substituted with one or more substituents selected from the group consisting of alkyl, alkoxy, halogen, CN, OH, CF 3 , OCF 3 , NH 2 , NH(CH 3 ) and N(CH 3 ) 2 .
10. The compound or salt according to claim 9 wherein Y is optionally substituted with CF 3 .
11. The compound or salt according to claim 2 wherein R a and R b are taken together with the nitrogen to form 2,3-dihydro-1H-isoindolyl, optionally substituted piperidinyl or optionally substituted pyrrolidinyl.
12. The compound or salt according to claim 11 wherein the optionally substituted piperidinyl or optionally substituted pyrrolidinyl is optionally substituted by substituents selected from the group consisting of optionally substituted cyclohexyl and optionally substituted phenyl.
13. The compound or salt according to claim 12 wherein Y is optionally substituted 5,6,7,8-tetrahydro[1,6]naphthyridinyl.
14. The compound or salt according to claim 13 wherein the optionally substituted piperidinyl is substituted with optionally substituted phenyl or optionally substituted pyrrolidinyl.
15. The compound or salt according to claim 14 wherein the optionally substituted piperidinyl is substituted with optionally substituted pyrrolidinyl.
16. The compound or salt according to claim 14 wherein the optionally substituted piperidinyl is substituted with optionally substituted phenyl.
17. The compound or salt according to claim 12 wherein the optionally substituted pyrrolidinyl is substituted by optionally substituted cyclohexyl.
18. A pharmaceutical composition comprising a compound of Formula (I)
or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient, wherein
R a is H or optionally substituted (C 1 -C 6 )alkyl;
R b is selected from the optionally substituted group consisting of —(CH 2 ) n -aryl, —CH(CH 3 )-aryl, —(CH 2 ) n -aryl-aryl, —(CH 2 ) n -aryl-heteroaryl, —(CH 2 ) n —(C 3 -C 8 )cycloalkyl, —(CH 2 ) n -heteroaryl, —(CH 2 ) n -heterocyclyl and —(C 3 -C 8 )cycloalkyl-aryl; or
R a and R b are taken together with the nitrogen to form 2,3-dihydro-1H-isoindolyl, decahydroisoquinolinyl, optionally substituted piperidinyl or optionally substituted pyrrolidinyl;
Y is selected from the optionally substituted group consisting of 5,6,7,8-tetrahydro[1,6]naphthyridinyl, —NH—(CH 2 ) n -heterocyclyl wherein the NH is attached to the carbonyl and -heterocyclyl-aryl wherein the heterocyclyl is attached to the carbonyl; and
n is 0, 1 or 2.
19. The compound or salt according to claim 1 , wherein the compound is selected from the group consisting of:
20. A pharmaceutical composition comprising a compound of claim 19 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.