IP Library Granted Patent US 7,317,125
Granted Patent B2
US 7,317,125 · App. 11/343,567 · Granted Jan 8, 2008

Diacylglycerol acyltransferase inhibitors

Assignee: Hoffman-La Roche Inc.
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Quick Facts
Patent No.
US 7,317,125
App. No.
11/343,567
Granted
Jan 8, 2008
Kind
B2
Abstract

Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, obesity, type II diabetes mellitus and metabolic syndrome.

Claims (43)

1. A compound of the formula (I):

wherein:

X is O or S;

R 1 is hydrogen, halogen, (C 1 -C 6 )alkyl or cyano;

R 2 , R 2′ are independently of each other H or halogen;

R 3 is unsubstituted phenyl, phenyl substituted with a group independently selected from the group consisting of halogen, (C 1 -C 6 ) alkyl, NH(CH 2 ) n CH(CH 3 ) 2 , or —O(CH 2 ) n OCH 3 , unsubstituted saturated, unsaturated or partially saturated heterocycyl which is a 5- or 6-membered heteroaromatic ring connected by a ring carbon atom which has from 1 to 3 hetero ring atoms selected from the group consisting of S, N and O, substituted saturated, unsaturated or partially saturated heterocycyl substituted with (C 1 -C 6 ) alkyl, or substituted or unsubstituted 5-10-membered carbocyclic ring;

R 4 is branched or unbranched (C 2 -C 6 ) alkyl, unsubstituted phenyl, phenyl mono-, di- or tri-substituted with a group independently selected from the group consisting of halogen, (C 1 -C 6 ) alkyl, (C 1 -C 6 ) alkoxy, —O(CH)(CH 3 ) 2 , —CF 3 , —O(CH 2 ) n CH 3 , —OCF 3 , —SCH 3 , —SO 2 CH 3 , —NO 2 , —(CH) 2 Ar, or unsubstituted or substituted 5-10 membered carbocyclic ring;

R 5 is (C 1 -C 6 ) alkyl;

n is 0, 1, 2 or 3,

or a pharmaceutically acceptable salt thereof.

2. The compound according to claim 1 , wherein R 3 is:

wherein Y is O or S.

3. The compound according to claim 1 , wherein X is O.

4. The compound according to claim 1 , wherein X is S.

5. The compound according to claim 1 , wherein R 4 is substituted phenyl which is phenyl mono-, di- or tri-substituted with a group independently selected from the group consisting of halogen, (C 1 -C 6 ) alkyl, (C 1 -C 6 ) alkoxy, —O(CH)(CH 3 ) 2 , —CF 3 , —O(CH 2 ) n CH 3 , —OCF 3 , —SCH 3 , —SO 2 CH 3 , and —NO 2 .

6. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(5-fluoro-2′-methoxy-biphenyl-2-yloxy)-acetyl]-N′-isopropyl-hydrazide.

7. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(5,2′-difluoro-biphenyl-2-yloxy)-acetyl]-N′-isopropyl-hydrazide.

8. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(5-fluoro-2′-methylsylfanyl-biphenyl-2-yloxy)-acetyl]-N′-isopropyl-hydrazide.

9. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(5-fluoro-2′-nitro-biphenyl-2-yloxy)-acetyl]-N′-isopropyl-hydrazide.

10. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(5-fluoro-2′-isopropoxy-biphenyl-2-yloxy)-acetyl]-N′-isopropyl-hydrazide.

11. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(2′-ethyl-5-fluoro-biphenyl-2-yloxy)-acetyl]-N′-isopropyl-hydrazide.

12. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(5-fluoro-2′-propoxy-biphenyl-2-yloxy)-acetyl]-N′-isopropyl-hydrazide.

13. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(2′-methoxycarbonyl-5-fluoro-biphenyl-2-yloxy)-acetyl]-N′-isopropyl-hydrazide.

14. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(2′-ethoxy-5-fluoro-biphenyl-2-yloxy)-acetyl]-N′-isopropyl hydrazide.

15. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(5-fluoro-2′-isopropyl-biphenyl-2-yloxy)-acetyl]-N′-isopropyl-hydrazide.

16. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(2′-ethyl-3,5-difluoro-biphenyl-2-yloxy)-acetyl]-N′-isopropyl-hydrazide.

17. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(5-methyl-2′-trifluoro-biphenyl-2-yloxy)-acetyl]-N′-isopropyl hydrazide.

18. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(4,5-difluoro-2′-trifluoromethoxy-biphenyl-2-yloxy)-acetyl]-N′-isopropyl hydrazide.

19. The compound according to claim 1 , wherein the compound is benzoic acid N′-[2-(3,5-difluoro-2′-trifluoromethoxy-biphenyl-2-yloxy)-acetyl]-N′-isopropyl hydrazide.

20. The compound according to claim 1 , wherein the compound is cyclohexanecarboxylic acid N′-[2-(5-fluoro-2′-trifluoromethoxy-biphenyl-2-yloxy)-acetyl]-N′-isopropyl-hydrazide.

21. The compound according to claim 1 , wherein the compound is thiophene-2-carboxylic acid N′-[2-(5-fluoro-2′-trifluoromethoxy-biphenyl-2-yloxy)-acetyl]-N′-isopropyl hydrazide.

22. A method for the treatment of obesity, type II diabetes or metabolic syndrome in a patient in need thereof, which comprises administering to said patient a therapeutically effective amount of a compound of the formula (I):

wherein:

X is O or S;

R 1 is hydrogen, halogen, (C 1 -C 6 )alkyl or cyano;

R 2 , R 2′ are independently of each other H or halogen;

R 3 is unsubstituted phenyl, substituted phenyl with a group independently selected from the group consisting of halogen, (C 1 -C 6 ) alkyl, NH(CH 2 ) n CH(CH 3 ) 2 , or —O(CH 2 ) n OCH 3 , unsubstituted saturated, unsaturated or partially saturated heterocycyl which is a 5- or 6-membered heteroaromatic ring connected by a ring carbon atom which has from 1 to 3 hetero ring atoms selected from the group consisting of S, N and O, substituted saturated, unsaturated or partially saturated heterocycyl substituted with (C 1 -C 6 ) alkyl, or substituted or unsubstituted 5-10-membered carboxylic ring;

R 4 is branched or unbranched (C 2 -C 6 ) alkyl, unsubstituted phenyl, substituted phenyl which is phenyl mono-, di- or tri-substituted with a group independently selected from the group consisting of halogen, (C 1 -C 6 ) alkyl, (C 1 -C 6 ) alkoxy, —O(CH)(CH 3 ) 2 , —CF 3 , —O(CH 2 ) n CH 3 , —OCF 3 , —SCH 3 , —SO 2 CH 3 , —NO 2 , —(CH) 2 Ar, or unsubstituted or substituted 5-10 membered carboxylic ring;

R 5 is (C 1 -C 6 ) alkyl;

n is 0, 1, 2 or 3,

or a pharmaceutically acceptable salt thereof.

23. The method according to claim 22 , wherein said therapeutically effective amount of said compound is in an amount of from about 10 mg to about 1000 mg per day.

24. A pharmaceutical composition comprising a compound or a pharmaceutically acceptable salt or ester thereof according to claim 1 , and a pharmaceutically acceptable carrier.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 17, 2009
From: HOFFMANN-LA ROCHE INC.
To: VIA PHARMACEUTICALS, INC.
Reel/Frame 022552/0847 →
Continuity (2)
Provisional Application 6065067100 · Feb 7, 2005
Related Publication 20060178532A1 · Aug 10, 2006