IP Library Granted Patent US 8,188,289
Granted Patent B2
US 8,188,289 · App. 11/685,674 · Granted May 29, 2012

Conformationally restricted urea inhibitors of soluble epoxide hydrolase

Assignee: The Regents of the University of California
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Quick Facts
Patent No.
US 8,188,289
App. No.
11/685,674
Granted
May 29, 2012
Kind
B2
Abstract

Inhibitors of the soluble epoxide hydrolase (sEH) are provided that incorporate multiple pharmacophores and are useful in the treatment of diseases.

Claims (49)

1. A compound having the formula:

wherein R 1 is a member selected from the group consisting of phenyl, cyclohexyl, cycloheptyl and adamantyl, wherein said phenyl is optionally substituted with from 1 to 2 substituents each independently selected from the group consisting of C 1 -C 8 alkyl, haloC 1 -C 8 alkyl, cyano, haloC 1 -C 8 alkoxy, C 1 -C 8 heteroalkyl, aryl, heteroaryl;

L is selected from the group consisting of —CO— and —SO 2 -;

R 4 is selected from the group consisting of H, C 1 -C 8 alkyl, arylC 0 -C 8 alkyl, and C 3 -C 12 cycloalkyl, each optionally substituted with from 1 to 2 substituents each independently selected from the group consisting of C 1 -C 8 alkyl, halo, C 1 -C 8 heteroalkyl, arylC 0 -C 8 alkyl, COR 6 , S(O) m R 6 and heteroaryl;

each R 6 is independently selected from the group consisting of H, C 1 -C 8 alkyl, C 1 -C 8 alkoxy and amino;

the subscript n is 0; and

the subscript m is an integer of from 0 to 2;

or a pharmaceutically acceptable salt thereof.

2. The compound in accordance with claim 1 having the formula:

or a pharmaceutically acceptable salt thereof.

3. The compound in accordance with claim 1 or 2 , wherein R 1 is adamantyl.

4. The compound in accordance with claim 1 or 2 , wherein R 1 is cycloheptyl or cyclohexyl.

5. The compound in accordance with claim 1 or 2 , wherein L is a —C(O)—.

6. The compound in accordance with claim 1 or 2 , wherein R 4 is selected from the group consisting of hydrogen, C 1 -C 8 alkyl, and arylC 0 -C 8 alkyl.

7. The compound in accordance with claim 1 or 2 , wherein R 4 is C 1 -C 8 alkyl.

8. A compound according to claim 2 which compound is selected from the group consisting of:

N-(1-acetylpiperidin-4-yl)-N′-(adamant-1-yl)urea;

N-(1-propionylpiperidin-4-yl)-N′-(adamant-1-yl)urea;

N-(1-butyrylpiperidin-4-yl)-N′-(adamant-1-yl)urea;

N-(1-benzoylpiperidin-4-yl)-N′-(adamant-1-yl)urea;

4-[4-(3-adamantan-1-yl-ureido)-piperidin-1-yl]-4-oxo-butanoic acid methyl ester;

5-[4-(3-adamantan-1-yl-ureido)-piperidin-1-yl]-5-oxo-pentanoic acid methyl ester;

2-[4-(3-adamantan-1-yl-ureido)-piperidine-1-carbonyl]-benzoic acid methyl ester;

3-[4-(3-adamantan-1-yl-ureido)-piperidine-1-carbonyl]-benzoic acid methyl ester;

4-[4-(3-adamantan-1-yl-ureido)-piperidine-1-carbonyl]-benzoic acid methyl ester;

1-(1-acetyl-piperidin-4-yl)-3-(4-trifluoromethoxyphenyl)urea;

1-(1-trifluoromethylcarbonylpiperidin-4-yl)-3-(4-trifluoromethoxyphenyl)urea; and

1-(1-acetyl-piperidin-4-yl)-3-cycloheptyl urea;

or a pharmaceutically acceptable salt thereof.

9. The compound according to claim 8 , wherein said compound is selected from the group consisting of:

N-(1-acetylpiperidin-4-yl)-N′-(adamant-1-yl)urea;

N-(1-propionylpiperidin-4-yl)-N′-(adamant-1-yl)urea;

N-(1-butyrylpiperidin-4-yl)-N′-(adamant-1-yl)urea; and

N-(1-benzoylpiperidin-4-yl)-N′-(adamant-1-yl)urea or a pharmaceutically acceptable salt thereof.

10. The compound according to claim 8 , wherein said compound is N-(1-acetylpiperidin-4-yl)-N′-(adamant-1-yl)urea or a pharmaceutically acceptable salt thereof.

11. The compound according to claim 8 , wherein said compound is N-(1-propionylpiperidin-4-yl)-N′-(adamant-1-yl)urea or a pharmaceutically acceptable salt thereof.

12. The compound according to claim 8 , wherein said compound is N-(1-butyrylpiperidin-4-yl)-N′-(adamant-1-yl)urea or a pharmaceutically acceptable salt thereof.

13. The compound according to claim 8 , wherein said compound is N-(1-benzoylpiperidin-4-yl)-N′-(adamant-1-yl)urea or a pharmaceutically acceptable salt thereof.

14. A compound according to claim 2 which compound is selected from the group consisting of:

N-(1-methanesulfonylpiperidin-4-yl)-N′-(adamant-1-yl)urea;

N-(1-methanesulfonylpiperidin-4-yl)-N′-(4-trifluoromethoxyphenyl)urea;

N-(1-toluene-4-sulfonylpiperidin-4-yl)-N′-(4-trifluoromethoxyphenyl)urea; and

N-[1-(5-dimethylaminonaphthalene-1-sulfonyl)-piperidin-4-yl]-N′-(4-trifluoromethoxy -phenyl) urea;

or a pharmaceutically acceptable salt thereof.

15. The compound according to claim 14 , wherein said compound is N-(1-methanesulfonylpiperidin-4-yl)-N′-(adamant-1-yl)urea or a pharmaceutically acceptable salt thereof.

16. The compound according to claim 14 , wherein said compound is N-(1-methanesulfonylpiperidin-4-yl)-N′-(4-trifluoromethoxy-phenyl)urea or a pharmaceutically acceptable salt thereof.

17. The compound according to claim 14 , wherein said compound is N-(1-toluene-4-sulfonylpiperidin-4-yl)-N′-(4-trifluoromethoxy-phenyl)urea or a pharmaceutically acceptable salt thereof.

18. The compound according to claim 14 , wherein said compound is N-[1-(5-dimethylaminonaphthalene-1-sulfonyl)-piperidin-4-yl]-N′-(4-trifluoromethoxy-phenyl) urea or a pharmaceutically acceptable salt thereof.

19. A pharmaceutical composition comprising a compound according to any one of claims 1 and 2 and a pharmaceutically acceptable excipient.

Assignments (5)
CONFIRMATORY LICENSE Recorded Jul 21, 2011
From: UNIVERSITY OF CALIFORNIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 026628/0127 →
CONFIRMATORY LICENSE Recorded May 26, 2010
From: UNIVERSITY OF CALIFORNIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024442/0686 →
ASSIGNMENT Recorded Mar 17, 2010
From: ARETE THERAPEUTICS, INC.
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 024093/0749 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 8, 2007
From: GLESS, RICHARD
To: ARETE THERAPEUTICS
Reel/Frame 019429/0861 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2007
From: HAMMOCK, BRUCE D.; JONES, PAUL D.; MORISSEAU, CHRISTOPHE; HUANG, HUAZHANG; TSAI, HSING-JU
To: REGENTS OF THE UNIVERSITY OF CALIFORNIA, THE
Reel/Frame 019198/0625 →
Continuity (2)
Provisional Application 60782172 · Mar 13, 2006
Related Publication 20070225283A1 · Sep 27, 2007