IP Library Granted Patent US 8,629,275
Granted Patent B2
US 8,629,275 · App. 13/060,775 · Granted Jan 14, 2014

AHCY hydrolase inhibitors for treatment of hyper homocysteinemia

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Quick Facts
Patent No.
US 8,629,275
App. No.
13/060,775
Granted
Jan 14, 2014
Kind
B2
Abstract

The present invention is directed to AHCY inhibitors of formula (I): which are useful in the treatment of diseases characterized by high homocysteine levels, such as Alzheimer's disease. The invention is also directed to pharmaceutical compositions comprising the compounds, and to the use of the compounds and compositions in the treatment of diseases characterized by high homocysteine levels.

Claims (66)

1. A compound of formula (I):

or a pharmaceutically acceptable salt thereof, wherein

X—Y is selected from the group consisting of

(1) CR 1 R 2 —CR 3 R 4 ,

(2) CR 1 ═CR 2 ;

Z is —CR 5 ;

Q is selected from the group consisting of

(1) hydrogen,

(2) halogen, and

(2) —C 1-6 alkyl;

R 1 , R 2 , R 3 and R 4 are each independently selected from the group consisting of

(1) hydrogen,

(2) hydroxyl,

(3) halogen,

(4) —C 1-6 alkyl, wherein said alkyl is optionally substituted with

(a) halogen, or

(b) hydroxyl;

R 5 is selected from the group consisting of

(1) hydrogen,

(2) —C 1-6 alkyl, and

(3) —C 3-6 cycloalkyl.

2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein Z is —CR 5 —, wherein R 5 is halogen.

3. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein X—Y is CR 1 R 2 —CR 3 R 4 .

4. The compound of claim 3 , or a pharmaceutically acceptable salt thereof, wherein each of R 1 , R 2 , R 3 and R 4 is selected from the group consisting of

(1) hydrogen, and

(2) —C 1-3 alkyl, wherein said alkyl is optionally substituted with

(a) halogen, or

(b) hydroxyl.

5. The compound of claim 4 , or a pharmaceutically acceptable salt thereof, wherein each of R 1 , R 2 , R 3 and R 4 is selected from the group consisting of

(1) hydrogen, and

(2) —CH 2 OH.

6. The compound of claim 5 , or a pharmaceutically acceptable salt thereof, wherein each of R 1 , R 2 , R 3 and R 4 is hydrogen.

7. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein X—Y is CR 1 ═CR 2 .

8. The compound of claim 7 , or a pharmaceutically acceptable salt thereof, wherein each of R 1 and R 2 is selected from the group consisting of

(1) hydrogen, and

(2) —C 1-3 alkyl, wherein said alkyl is optionally substituted with

(a) halogen, or

(b) hydroxyl.

9. The compound of claim 8 , or a pharmaceutically acceptable salt thereof, wherein each of R 1 and R 2 is selected from the group consisting of

(1) hydrogen, and

(2) —CH 2 OH.

10. The compound of claim 7 , or a pharmaceutically acceptable salt thereof, wherein X—Y is CH═CR 2 , wherein R 2 is selected from the group consisting of

(1) hydrogen, and

(2) —C 1-3 alkyl, wherein said alkyl is optionally substituted with

(a) halogen, or

(b) hydroxyl.

11. The compound of claim 7 , or a pharmaceutically acceptable salt thereof, wherein X—Y is —CH═CH—.

12. The compound of claim 1 , wherein R 5 is selected from the group consisting of

(1) halogen, and

(2) —C 1-3 alkyl, wherein said alkyl is optionally substituted with

(a) halogen, or

(b) hydroxyl.

13. The compound of claim 1 , wherein Q is hydrogen or halogen.

14. The compound of claim 13 , wherein Q is hydrogen.

15. The compound of claim 1 , which is selected from the group consisting of

(1R,2S,3R)-3-(4-amino-7-fluoro-1H-imidazo[4,5-c]pyridin-1-yl)cyclopentane-1,2-diol (1); (1R,2S,3R)-3-(4-amino-7-chloro-1H-imidazo[4,5-c]pyridin-1-yl)cyclopentane-1,2-diol(1-11);

(1R,2S,3R)-3-(4-amino-7-methyl-1H-imidazo[4,5-c]pyridin-1-yl)cyclopentane-1,2-diol(1-12);

(1R,2S,3R)-3-(4-amino-6,7-difluoro-1H-imidazo[4,5-c]pyridin-1-yl)cyclopentane-1,2-diol(1-15);

(1R,2R,5R)-5-(4-amino-7-chloro-1H-imidazo[4,5-c]pyridin-1-yl)cyclopent-3-ene-1,2-diol(2-7);

(1R,2R,5R)-5-(4-amino-7-methyl-1H-imidazo[4,5-c]pyridin-1-yl)cyclopent-3-ene-1,2-diol (2-8);

(1R,2R,3S,4R)-4-(4-amino-7-fluoro-1H-imidazo[4,5-c]pyridin-1-yl)cyclopentane-1,2,3-triol(3);

(1R,2S,3R,5S)-3-(4-amino-7-fluoro-1H-imidazo[4,5-c]pyridin-1-yl)-5-fluorocyclopentane-1,2-diol(4);

(1R,2S,3S)-3-(4-amino-7-fluoro-1H-imidazo[4,5-c]pyridin-1-yl)-4-fluorocyclopentane-1,2-diol(5);

(1R,2S,3R,5S)-3-(4-amino-7-fluoro-3a,7a-dihydro-1H-imidazo[4,5-c]pyridin-1-yl)-5-methylcyclopentane-1,2-diol(6);

or a pharmaceutically acceptable salt thereof.

16. A pharmaceutical composition comprising a compound of claim 1 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

Assignments (3)
CHANGE OF NAME Recorded Aug 29, 2012
From: SCHERING CORPORATION
To: MERCK SHARP & DOHME CORP.
Reel/Frame 028866/0511 →
MERGER Recorded Aug 27, 2012
From: MERCK SHARP & DOHME CORP.
To: SCHERING CORPORATION
Reel/Frame 028850/0515 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 25, 2011
From: CONVERSO, ANTONELLA; FRALEY, MARK E.; HARTINGH, TIMOTHY J.
To: MERCK SHARP & DOHME CORP
Reel/Frame 025868/0984 →