IP Library Granted Patent US 7,429,663
Granted Patent B2
US 7,429,663 · App. 10/504,679 · Granted Sep 30, 2008

7-(Pyrimidin-4-yl)-Imidazo[1,2-a]Pyrimidin-5(1H)-ones as GSK3β inhibitors

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Quick Facts
Patent No.
US 7,429,663
App. No.
10/504,679
Granted
Sep 30, 2008
Kind
B2
Abstract

The invention relates to a imidazo[1,2-a]pyrimidone derivative represented by formula (I) or a salt thereof: R 1 wherein X represents a bond, an ethenylene group, an ethenylene group, a methylene group optionally substituted; a carbonyl group, an oxygen atom, a sulfur atom, a sulfonyl group, a sulfoxide group or a nitrogen atom being optionally substituted; R 1 represents a 2, 4 or 5-pyrimidinyl optionally substituted; R 2 represents a C 1-6 alkyl group, a C 1-2 perhalogenated alkyl group,a C 1-3 halogenated alkyl group, a benzyl group, a benzene ring, a naphthalene ring, 5,6,7,8-tetrahydronaphthalene ring, a pyridine ring, an indole ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring, the benzyl group and the rings being optionally substituted; and n represents 0 to 3. The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β, such as Alzheimer disease.

Claims (29)

1. A compound of formula (I) or a pharmaceutically acceptable salt thereof:

wherein:

X represents a covalent single bond, an ethenylene group, an ethynylene group, a methylene group optionally substituted by one or two groups selected from a C 1-6 alkyl group, a hydroxy group and a C 1-4 alkoxy group; a carbonyl group, an oxygen atom, a sulfur atom, a sulfonyl group, a sulfoxide group or a nitrogen atom being optionally substituted by a C 1-6 alkyl group;

R 1 represents a 2, 4 or 5-pyrimidinyl optionally substituted by a C 1-4 alkyl group, C 1-4 alkoxy group or a halogen atom;

R 2 represents a C 1-6 alkyl group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a benzyl group, a benzene ring, a naphthalene ring, 5,6,7,8-tetrahydronaphthalene ring, a pyridine ring, an indole ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring, the benzyl group and the rings being optionally substituted by 1 to 4 substituents selected from a C 1-6 alkyl group, a benzene ring, a halogen atom, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a hydroxyl group, a C 1-4 alkoxy group, a nitro, a cyano, an amino, a C 1-6 monoalkylamino group or a C 2-10 dialkylamino group; and

n represents 0 to 3.

2. The compound of formula (I) according to claim 1 , wherein R 1 represents an unsubstituted 4-pyrimidine ring.

3. The compound of formula (I) according to claim 1 , wherein R 2 is a benzene ring, a naphthalene ring, or a 5,6,7,8-tetrahydronaphthalene ring, the rings being optionally substituted by 1 to 4 substituents selected from a C 1-6 alkyl group, a benzene ring, a halogen atom, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a hydroxyl group, a C 1-4 alkoxy group, a nitro, a cyano, an amino, a C 1-6 monoalkylamino group or a C 2-10 dialkylamino group.

4. A compound selected from the group consisting of:

1-(3-Phenyl-propyl)-7-(pyrimidin-4-yl)-1 H-imidazo[1,2-a]pyrimidin-5-one;

1-[3-(2-Fluoro-phenyl)-propyl]-7-(pyrimidin-4-yl)-1 H-imidazo[1,2-a]pyrimidin-5-one;

1-[2-(4-Fluoro-2-methoxy-phenyl)-ethyl]-7-(pyrimidin-4-yl )-1 H-imidazo[1,2-a]pyrimidin-5-one;

1-[2-(4-Methoxy-phenyl)-ethyl]-7-(pyrimidin-4-yl)-1 H-imidazo[1,2-a]pyrimidin-5-one;

1-[2-(4-methyl-phenyl)-ethyl]-7-(pyrimidin-4-yl)-1 H-imidazo[1,2-a]pyrimidin-5-one;

1-(2-Naphthalen-1-yl-ethyl)-7-(pyrimidin-4-yl)-1 H-imidazo[1,2-a]pyrimidin-5-one;

1-[2(3-Fluoro-phenyl)-ethyl]7-(pyrimidin-4yl )-1 H-imidazo[1,2-a]pyrimidin-5-one;

1-[2-(3-Chloro-phenyl)-ethyl]-7-(pyrimidin-4-yl)-1 H-imidazo[1,2-a]pyrimidin-5-one;

1-[2-(2-Methoxy-phenyl)-ethyl]7-(pyrimidin4-yl)-1 H-imidazo[1,2-a]pyrimidin-5-one;

4-[2-[5-Oxo-7-(pyrimidin-4-yl)-5H-imidazo[1,2-a]pyrimidin-1-yl]-ethyl]-benzonitrile;

1-(2-Hydroxy-2phenylethyl)-7-(pyrimidin-4-yl)-1 H-imidazo[1,2-a]pyrimidin-5-one;

1-(2-Oxo-2-phenyl-ethyl)-7-(pyrimidin-4-yl)-1 H-imidazo[1,2-a]pyrimidin-5-one;

1-[2(4-Fluoro-phenyl)-ethyl]-7-(pyrimidin4yl)-1 H-imidazo[1,2-a]pyrimidin-5-one;

1-[2-(4-Ethoxy-phenyl)-ethyl]-7-(pyrimidin-4-yl)-1 H-imidazo[1,2-a]pyrimidin-5-one; and

1-[2-(2,5-Dimethoxy-phenyl)-ethyl]-7-(pyrimidin-4-yl)-1 H-imidazo[1,2-a]pyrimidin-5-one;

or a pharmaceutically acceptable salt thereof.

5. A compound of formula (III):

wherein:

R 1 represents a 2, 4 or 5-pyrimidinyl optionally substituted by a C 1-4 alkyl group, C 1-4 alkoxy group or a halogen atom.

6. The compound of formula (I) according to claim 2 , wherein R 2 is a benzene ring, a naphthalene ring, or a 5,6,7,8-tetrahydronaphthalene ring, the rings being optionally substituted by 1 to 4 substituents selected from a C 1-6 alkyl group, a benzene ring, a halogen atom, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a hydroxyl group, a C 1-4 alkoxy group, a nitro, a cyano, an amino, a C 1-6 monoalkylamino group or a C 2-10 dialkylamino group.

Assignments (3)
CHANGE OF NAME Recorded Jun 20, 2012
From: SANOFI-AVENTIS
To: SANOFI
Reel/Frame 028413/0927 →
CHANGE OF NAME Recorded Jul 22, 2005
From: SANOFI-SYNTHELABO
To: SANOFI-AVENTIS
Reel/Frame 016345/0189 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2005
From: LOCHEAD, ALISTAIR; SAADY, MOURAD; YAICHE, PHILIPPE
To: SANOFI-AVENTIS; MITSUBISHI PHARMA CORPORATION
Reel/Frame 016211/0779 →