IP Library Granted Patent US 7,932,245
Granted Patent B2
US 7,932,245 · App. 10/691,095 · Granted Apr 26, 2011

Spirocyclopropyl amides and acids and their therapeutic applications

Assignee: Abbott Laboratories
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Quick Facts
Patent No.
US 7,932,245
App. No.
10/691,095
Granted
Apr 26, 2011
Kind
B2
Abstract

The present invention relates to the use of compounds of formula (I) for the treatment of epilepsy, bipolar disorder, psychiatric disorders, migraine, pain, or movement disorders, and to provide neuroprotection.

Claims (59)

1. A method of treating migraine, epilepsy, or bipolar disorder in a mammal comprising administering to a mammal a therapeutically effective amount of a compound of formula (I)

wherein

A is cyclohexyl optionally substituted with 1, 2, 3, or 4 alkyl groups;

R A , R B , and R C are independently hydrogen or alkyl;

R 1 is OR 2 or NR 3 R 4 ;

R 2 is hydrogen;

R 3 and R 4 are independently hydrogen, carboxyalkyl, hydroxyalkyl, or (NR 5 R 6 )carbonylalkyl;

and

R 5 and R 6 are hydrogen.

2. The method according to claim 1 wherein R 1 is OR 2 .

3. The method according to claim 1 wherein

R 1 is OR 2 .

4. The method according to claim 3 wherein the compound of formula (I) is

spiro[2.5]octane-1-carboxylic acid;

(1S)-spiro[2.5]octane-1-carboxylic acid;

(1R)-spiro[2.5]octane-1-carboxylic acid;

2-methylspiro[2.5]octane-1-carboxylic acid;

5,7-dimethylspiro[2.5]octane-1-carboxylic acid;

6-tert-butylspiro[2.5]octane-1-carboxylic acid;

(4S3R)-4-isopropyl-7-methylspiro[2.5]octane-1-carboxylic acid; or

5,5,7,7-tetramethylspiro[2.5]octane-1-carboxylic acid.

5. The method according to claim 1 wherein

R 1 is NR 3 R 4 .

6. The method according to claim 1 wherein

R 1 is NR 3 R 4 ;

R 4 is hydrogen or (NR 5 R 6 )carbonylalkyl; and

R 3 is hydrogen.

7. The method according to claim 6 wherein the compound of formula (I) is

spiro[2.5]octane-1-carboxamide;

N-(2-amino-2-oxoethyl)spiro[2.5]octane-1-carboxamide;

(1S)—N-[(1S)-2-amino-1-methyl-2-oxoethyl]spiro[2.5]octane-1-carboxamide;

(1R)—N-[(1S)-2-amino-1-methyl-2-oxoethyl]spiro[2.5]octane-1-carboxamide;

(1S)-spiro[2.5]octane-1-carboxamide;

(1R)-spiro[2.5]octane-1-carboxamide;

2-methyl spiro[2.5]octane-1-carboxamide;

N-(2-amino-2-oxoethyl)-2-methylspiro[2.5]octane-1-carboxamide;

5,7-dimethylspiro[2.5]octane-1-carboxamide;

N-(2-amino-2-oxoethyl)-5,7-dimethylspiro[2.5]octane-1-carboxamide;

6-tert-butylspiro[2.5]octane-1-carboxamide;

N-(2-amino-2-oxoethyl)-6-tert-butylspiro[2.5]octane-1-carboxamide;

(4S,7R)-4-isopropyl-7-methylspiro[2.5]octane-1-carboxamide;

(4S,7R)—N-(2-amino-2-oxoethyl)-4-isopropyl-7-methylspiro[2.5]octane-1-carboxamide;

N-(3-amino-3-oxopropyl)spiro[2.5]octane-1-carboxamide;

5,5,7,7-tetramethylspiro[2.5]octane-1-carboxamide; or

N-(2-amino-2-oxoethyl)-5,5,7,7-tetramethylspiro[2.5]octane-1-carboxamide.

8. The method according to claim 6 wherein the compound of formula (I) is (1S)—N-(2-amino-2-oxoethyl)spiro[2.5]octane-1-carboxamide.

9. The method according to claim 6 wherein the compound of formula (I) is (1R)—N-(2-amino-2-oxoethyl)spiro[2.5]octane-1-carboxamide.

10. The method according to claim 1 wherein

R 1 is NR 3 R 4 ;

R 4 is carboxyalkyl or hydroxyalkyl; and

R 3 is hydrogen.

11. The method according to claim 10 wherein the compound of formula (I) is

[(spiro[2.5]oct-1-ylcarbonyl)amino]acetic acid;

{[(1S)-spiro[2.5]oct-1-ylcarbonyl]amino}acetic acid;

{[(1R)-spiro[2.5]oct-1-ylcarbonyl]amino}acetic acid;

(1R)—N-[(2R)-2-hydroxypropyl]spiro[2.5]octane-1-carboxamide;

(1R)—N-[(2S)-2-hydroxypropyl]spiro[2.5]octane-1-carboxamide;

(1S)—N-[(2R)-2-hydroxypropyl]spiro[2.5]octane-1-carboxamide; or

(1S)—N-[(2S)-2-hydroxypropyl]spiro[2.5]octane-1-carboxamide.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2013
From: ABBOTT LABORATORIES
To: ABBVIE INC.
Reel/Frame 030176/0968 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 16, 2004
From: BENNANI, YOUSSEF L.; BUNNELLE, WILLIAM H.; CHANG, SOU-JEN; CHEMBURKAR, SANJAY P.; DART, MICHAEL J.; KU, YI-YIN; CHEN, JINHUA; FERNANDO, DILINIE P.; LOCKWOOD, MARK; WANG, LEI
To: ABBOTT LABORATORIES
Reel/Frame 015062/0852 →
Continuity (2)
Provisional Application 60420286 · Oct 22, 2002
Related Publication 20040204396A1 · Oct 14, 2004