IP Library Granted Patent US 7,618,970
Granted Patent B2
US 7,618,970 · App. 11/167,329 · Granted Nov 17, 2009

3-aminocyclopentanecarboxamides as modulators of chemokine receptors

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Quick Facts
Patent No.
US 7,618,970
App. No.
11/167,329
Granted
Nov 17, 2009
Kind
B2
Abstract

The present invention is directed to compounds of Formula I: which are modulators of chemokine receptors. The compounds of the invention, and compositions thereof, are useful in the treatment of diseases related to chemokine receptor expression and/or activity.

Claims (82)

1. A compound of Formula I:

or pharmaceutically acceptable salt thereof, wherein:

a dashed line indicates an optional bond;

W is:

V is N, NO or CR 5 ;

X is N, NO or CR 2 ;

Y is N, NO or CR 3 ;

Z is N, NO or CR 4 ; wherein no more than one of V, X, Y and Z is NO;

R A , R A1 , R B and R B1 are each, independently, H, OH, halo, C 1-6 alkyl, C 1-6 alkenyl, C 1-6 alkynyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, heterocyclyl, carbocyclyl, NR 10 R 12 , NR 10 CO 2 R 11 ; NR 10 CONR 10 R 12 , NR 10 SO 2 NR 10 R 12 , NR 10 —SO 2 —R 11 , CN, CONR 10 R 12 , CO 2 R 10 , NO 2 , SR 10 , SOR 10 , SO 2 R 10 , or SO 2 —NR 10 R 12 ;

R 1 is C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 hydroxyalkyl, —(C 0-6 alkyl)-O—(C 1-6 alkyl), —(C 0-6 alkyl)-S—(C 1-6 alkyl), —(C 0-6 alkyl)-(C 3-7 cycloalkyl)-(C 0-6 alkyl), OH, OR 10 , SR 10 , COR 11 , CO 2 R 10 , CONR 10 R 12 , carbocyclyl, heterocyclyl, CN, NR 10 R 12 , NR 10 SO 2 R 10 , NR 10 COR 10 , NR 10 CO 2 R 10 , NR 10 CONR 12 , CR 10 R 11 CO 2 R 10 or CR 10 R 11 OCOR 10 ;

R 2 , R 3 , R 4 , R 5 and R 6 are each, independently, H, OH, halo, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, C 1-6 thioalkoxy, NR 10 R 12 , NR 10 CO 2 R 11 ; NR 10 CONR 10 R 12 , NR 10 SO 2 NR 10 R 12 , NR 10 —SO 2 —R 11 , heterocyclyl, carbocyclyl, carbocyclyloxy, heterocyclyloxy, CN, NO 2 , COR 11 , CONR 10 R 12 , CO 2 R 10 , NO 2 , SR 10 , SOR 10 , SO 2 R 10 ; or SO 2 —NR 10 R 12 ;

R 7 is H or C 1-6 alkyl optionally substituted by 1-3 substituents selected from halo, OH, CO 2 H, CO 2 —(C 1-6 alkyl), or C 1-3 alkoxy;

R 8 is C 1-3 alkoxy, C 1-3 haloalkoxy, C 3-6 cycloalkyloxy or OH;

R 8′ is H;

R 9 and R 9′ are each, independently, H, C 1-6 alkyl, halo, C 1-3 alkoxy, C 1-3 haloalkoxy, C 3-6 cycloalkyl, C 3-6 cycloalkyloxy, OH, CO 2 R 10 , OCOR 10 , wherein said C 1-6 alkyl is optionally substituted with one or more substituents selected from F, C 1-3 alkoxy, OH or CO 2 R 10 ;

or R 9 and R 9′ together with the carbon atom to which they are attached form a 3-7 membered spirocyclyl group;

R 10 is H, C 1-6 alkyl, benzyl, phenyl, or C 3-6 cycloalkyl, wherein said C 1-6 alkyl, benzyl, phenyl, or C 3-6 cycloalkyl is optionally substituted with 1-3 selected from halo, OH, C 1-3 alkyl, C 1-3 haloalkyl, C 1-3 alkoxy, C 1-3 haloalkoxy, CO 2 H, and CO 2 —(C 1-6 alkyl);

R 11 is H, OH, C 1-6 alkyl, C 1-6 alkoxy, benzyl, phenyl, benzyloxy, phenyloxy, C 3-6 cycloalkyl or C 3-6 cycloalkyloxy, wherein said C 1-6 alkyl, C 1-6 alkoxy, benzyl, phenyl, benzyloxy, phenyloxy, C 3-6 cycloalkyl or C 3-6 cycloalkyloxy, is optionally substituted with 1-3 substituents selected from halo, OH, C 1-3 alkyl, C 1-3 alkoxy, CO 2 H, CO 2 —(C 1-6 alkyl) and CF 3 ;

R 12 is H, C 1-6 alkyl, benzyl, phenyl, or C 3-6 cycloalkyl, wherein said C 1-6 alkyl, benzyl, phenyl, or C 3-6 cycloalkyl is optionally substituted with 1-3 selected from halo, OH, C 1-3 alkyl, C 1-3 haloalkyl, C 1-3 alkoxy, C 1-3 haloalkoxy, CO 2 H, and CO 2 —(C 1-6 alkyl); and

p is 0 or 1.

2. The compound of claim 1 wherein W is

3. The compound of claim 1 wherein V is CR 5 .

4. The compound of claim 1 wherein X is CR 2 .

5. The compound of claim 1 wherein Y is CR 3 .

6. The compound of claim 1 wherein Z is CR 4 .

7. The compound of claim 1 wherein X is CR 2 ; Y is CR 3 ; and Z is CR 4 .

8. The compound of claim 1 wherein V is CR 5 , X is CR ; Y is CR 3 ; and Z is CR 4 .

9. The compound of claim 1 wherein R A , R A1 , R B and R B1 are each, independently, H,OH, halo, C 1-6 alkyl, C 1-6 alkenyl, C 1-6 alkynyl, C 1-6 haloalkyl, C 1-6 alkoxy or C 1-6 haloalkoxy.

10. The compound of claim 1 wherein R A , R A1 , R B and R B1 are each, independently, H,OH or C 1-6 alkoxy.

11. The compound of claim 1 wherein R A , R A1 , R B and R B1 are each, independently, H or OH.

12. The compound of claim 1 wherein R 1 is C 1-6 alkyl, C 1-6 hydroxyalkyl, —(C 0-6 alkyl)-O—(C 1-6 alkyl), or heterocyclyl.

13. The compound of claim 1 wherein R 1 is C 1-6 alkyl.

14. The compound of claim 1 wherein R 1 is prop-2-yl.

15. The compound of claim 1 wherein one of R 5 and R 6 is other than H.

16. The compound of claim 1 wherein one of R 5 and R 6 is C 1-4 haloalkyl.

17. The compound of claim 1 wherein R 6 is C 1-4 haloalkyl.

18. The compound of claim 1 wherein R 6 is CF 3 .

19. The compound of claim 1 wherein R 7 is H.

20. The compound of claim 1 wherein R 8 is C 1-3 alkoxy or C 1-3 haloalkoxy.

21. The compound of claim 1 wherein R 8 is C 1-3 alkoxy.

22. The compound of claim 1 wherein R 8 is methoxy.

23. The compound of claim 1 wherein R 8 is ethoxy.

24. The compound of claim 1 wherein R 9 and R 9′ are both H.

25. The compound of claim 1 having Formula Ie or If:

26. The compound of claim 1 having the Formula Ig:

27. The compound of claim 1 having the Formula Ih or Ii:

28. The compound of claim 1 which is selected from:

N-[(1R,3S)-3-Isopropyl-3-({4-[3-(trifluoromethyl)phenyl]piperazin-1-yl}carbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

3-Ethoxy-N-[(1R,3S)-3-isopropyl-3-({4-[3-(trifluoromethyl)phenyl]piperazin-1-yl}carbonyl)cyclopentyl]tetrahydro-2H-pyran-4-amine;

N-[(1R,3S)-3-Isopropyl-3-({4-[4-(trifluoromethyl)pyridin-2-yl]piperazin-1-yl}carbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

N-[(1R,3S)-3-Isopropyl-3-({4-[5-(trifluoromethyl)pyridin-3-yl]piperazin-1-yl}carbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

N-{(1R,3S)-3-Isopropyl-3-[(4-phenyl-3,6-dihydropyridin-1(2H)-yl)carbonyl]cyclopentyl} -3-methoxytetrahydro-2H-pyran-4-amine;

1-({(1S,3R)-1-Isopropyl-3-[(3-methoxytetrahydro-2H-pyran-4-yl)amino]cyclopentyl} carbonyl)-4-phenylpiperidin-4-ol;

1-({(1S,3R)-1-Isopropyl-3-[(3-methoxytetrahydro-2H-pyran-4-yl)amino]cyclopentyl}carbonyl)-4-[2-(trifluoromethyl)phenyl]piperidin-4-ol;

1-[((1S,3R)-1-Isopropyl-3-{[3-methoxytetrahydro-2H-pyran-4-yl]amino}cyclopentyl)carbonyl]-4-[3-(trifluoromethyl)phenyl]piperidin-4-ol;

1-[((1S,3R)-1-Isopropyl-3-{[3-methoxytetrahydro-2H-pyran-4-yl]amino}cyclopentyl)carbonyl]-4-[4-(trifluoromethyl)phenyl]piperidin-4-ol

N-((1R,3S)-3-Isopropyl-3-{[4-[2-(trifluoromethyl)phenyl]-3,6-dihydropyridin-1(2H)-yl]carbonyl}cyclopentyl)-3-methoxytetrahydro-2H-pyran-4-amine;

N-((1R,3S)-3-Isopropyl-3-{[4-[3-(trifluoromethyl)phenyl]-3,6-dihydropyridin-1(2H)-yl]carbonyl}cyclopentyl)-3-methoxytetrahydro-2H-pyran-4-amine;

3-Ethoxy-N-((1R,3S)-3-isopropyl-3-{[4-[3-(trifluoromethyl)phenyl]-3,6-dihydropyridin-1(2H)-yl]carbonyl }cyclopentyl)tetrahydro-2H-pyran-4-amine;

N-((1R,3S)-3-Isopropyl-3-{[4-(trifluoromethyl)-3′, 6′-dihydro-2,4′-bipyridin-1′(2′H)-yl]carbonyl}cyclopentyl)-3-methoxytetrahydro-2H-pyran-4-amine;

N-((1R,3S)-3-Isopropyl-3-{[5-(trifluoromethyl)-3′,6′-dihydro-3,4′-bipyridin-1′(2′H)-yl]carbonyl}cyclopentyl)-3-methoxytetrahydro-2H-pyran-4-amine;

N-[(1R,3S)-3-Isopropyl-3-({4-[4-(trifluoromethyl)pyrimidin-2-yl]piperazin-1-yl}carbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

N-[(1R,3S)-3-isopropyl-3-({4-[6-(trifluoromethyl)pyridin-2-yl]piperazin-1-yl}carbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

N-[(1R,3S)-3-isopropyl-3-(4-[6-(trifluoromethyl)pyrimidin-4-yl]piperazin-1-ylcarbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

N-[(1R,3S)-3-isopropyl-3-(4-[6-methyl-4-(trifluoromethyl)pyridin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

(4R)-N-[(1R,3S)-3-isopropyl-3-(4-[3-(trifluoromethyl)phenyl]piperidin-1-ylcarbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

2-[(1R,3S)-3-[(3-methoxytetrahydro-2H-pyran-4-yl)amino]-1-(4-[4-(trifluoromethyl)pyridin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]propan-2-ol;

2-[(1R,3S)-3-[(4R)-3-methoxytetrahydro-2H-pyran-4-yl]amino-1-(4-[4-(trifluoromethyl)pyrimidin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]propan-2-ol;

2-[(1S,3S)-3-[(3-methoxytetrahydro-2H-pyran-4-yl)amino]-1-(4-[6-(trifluoromethyl)pyridin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]propan-2-ol;

N-[(1S,3S)-3-ethyl-3-(4-[4-(trifluoromethyl)pyridin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

(4R)-N-[(1R,3S)-3-ethyl-3-(4-[4-(trifluoromethyl)pyrimidin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

N-[(1S,3S)-3-ethyl-3-(4-[6-(trifluoromethyl)pyridin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

(4R)-N-[(1R,3S)-3-methyl-3-(4-[4-(trifluoromethyl)pyrimidin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

(4R)-3-methoxy-N-[(1R,3S)-3-(2-methoxyethyl)-3-(4-[4-(trifluoromethyl)pyridin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]tetrahydro-2H-pyran-4-amine;

3-methoxy-N-[(1S,3S)-3-(2-methoxyethyl)-3-(4-[4-(trifluoromethyl)pyrimidin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]tetrahydro-2H-pyran-4-amine;

(4R)-N- [(1R,3S)-3-(ethoxymethyl)-3-(4-[4-(trifluoromethyl)-pyrimidin-2-yl]piperazin-1-ylcarbonyl) cyclopentyl]-3-tetrahydro-2H-pyran-4-amine;

(4R)-N-[(1R,3S)-3-(ethoxymethyl)-3-(4-[4-(trifluoromethyl)pyrimidin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]-3-methoxytetrahydro-2H-pyran-4-amine;

(4R)-3-methoxy-N-[(1R,3S)-3-(methoxymethyl)-3-(4-[4-(trifluoromethyl)pyridin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]tetrahydro-2H-pyran-4-amine;

(4R)-3-methoxy-N-[(1R,3S)-3-(methoxymethyl)-3-(4-[4-(trifluoromethyl)-pyrimidin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]tetrahydro-2H-pyran-4-amine;

(4R)-3-methoxy-N-[(1R,3S)-3-[(3R)-tetrahydrofuran-3-yl]-3-(4-[4-(trifluoromethyl)-pyrdin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]tetrahydro-2H -pyran-4-amine; and

(4R)-3-methoxy-N-[(1R,3S)-3-[(3R)-tetrahydrofuran-3-yl]-3-(4-[4-(trifluoromethyl)pyrimidin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]tetrahydro-2H-pyran-4-amine; or pharmaceutically acceptable salt thereof.

29. A composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier.

Assignments (6)
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY INFORMATION PREVIOUSLY RECORDED ON REEL 035920 FRAME 0576. ASSIGNOR(S) HEREBY CONFIRMS THE RECEIVING PARTY NAME SHOULD BE RECORDED AS TWO PARTIES. Recorded Jul 2, 2015
From: INCYTE CORPORATION
To: INCYTE HOLDINGS CORPORATION; INCYTE CORPORATION
Reel/Frame 036054/0740 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2015
From: INCYTE CORPORATION
To: INCYTE HOLDINGS CORPORATION AND INCYTE CORPORATION
Reel/Frame 035920/0576 →
CONFIRMATORY LICENSE Recorded Mar 20, 2006
From: INCYTE CORPORATION
To: PFIZER INC.
Reel/Frame 017351/0136 →
DOCUMENT PREVIOUSLY RECORDED AT REEL 016854 FRAME 0496 CONTAINED ERRORS IN PATENT APPLICATION NUMBER 11/167,328. DOCUMENT RERECORDED TO CORRECT ERRORS ON STATED REEL. Recorded Dec 20, 2005
From: XUE, CHU-BIAO; ZHENG, CHANGSHENG; FENG, HAO; XIA, MICHAEL; GLENN, JOSEPH; CAO, GANFENG; METCALF, BRIAN W.
To: INCYTE CORPORATION
Reel/Frame 017134/0689 →
SECURITY AGREEMENT Recorded Nov 30, 2005
From: INCYTE CORPORATION
To: PFIZER INC.
Reel/Frame 017281/0496 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 6, 2005
From: XUE, CHU-BIAO; ZHENG, CHANGSHENG; FENG, HAO; XIA, MICHAEL; GLENN, JOSEPH; CAO, GANFENG; METCALF, BRIAN W.
To: INCYTE CORPORATION
Reel/Frame 016854/0496 →