IP Library Granted Patent US 8,748,621
Granted Patent B2
US 8,748,621 · App. 13/556,547 · Granted Jun 10, 2014

1,3-disubstituted 4-(aryl-X-phenyl)-

Inventors: Jose Maria Cid-Nunez (Toledo, ES); Andres Avelino Trabanco-Suarez (Toledo, ES); Gregor James MacDonald (Beerse, BE); Guillaume Albert Jacques Duvey (Geneva, CH); Robert Johannes Lutjens (Geneva, CH); Patrick Terry Finn (Geneva, CH)
Assignees: Janssen Pharmaceuticals, Inc.; Addex Pharma, SA
C07D213/64
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Quick Facts
Patent No.
US 8,748,621
App. No.
13/556,547
Granted
Jun 10, 2014
Kind
B2
Abstract

The present invention relates to a method of treating, ameliorating, or controlling a condition in a mammal, including a human, wherein the condition is selected from the group consisting of anxiety disorders, psychotic disorders, substance-dependence related disorders, mood disorders, epilepsy or convulsive disorders, idiopathic Parkinson's disease, and Alzheimer's disease, wherein the method comprises administering to the mammal an effective amount of a compound of Formula (I) wherein all radicals are as defined in the application and claims. In particular, such conditions are central nervous system disorders selected from the group of anxiety, schizophrenia, depression, and epilepsy.

Claims (39)

1. A method for treating, ameliorating, or controlling a central nervous system disorder in a human, selected from the group consisting of anxiety disorders, psychotic disorders selected from the group consisting of schizophrenia, schizoaffective disorder and schizophreniform disorder, mood disorders, epilepsy or convulsive disorders, and dementia of the Alzheimer's type, wherein the method comprises administering to the human an effective amount of a compound having the formula (I)

or a stereochemically isomeric form thereof, wherein

R 1 is C 1-6 alkyl; or C 1-3 alkyl substituted with C 3-7 cycloalkyl, phenyl, or phenyl substituted with halo, trifluoromethyl or trifluoromethoxy;

R 2 is halo, trifluoromethyl, C 1-3 alkyl or cyclopropyl;

R 3 is hydrogen or halo;

X is O, S, SO, SO 2 , or CF 2 ; and

Ar is unsubstituted phenyl; unsubstituted pyridinyl; or phenyl or pyridinyl substituted with one or two substituents selected from the group consisting of halo, C 1-3 alkyl, C 1-3 alkoxy, trifluoromethyl, hydroxyC 1-3 alkyl and (CH 2 ) n —CO 2 H, wherein n=0, 1, or 2;

or a pharmaceutically acceptable salt thereof, provided that when R 3 is 2′-fluoro then Ar is not 3-pyridinyl substituted with one or two C 1-3 alkyl substituents.

2. The method according to claim 1 wherein

R 1 is 1-butyl, 2-methyl-1-propyl, 3-methyl-1-butyl, (cyclopropyl)methyl or 2-(cyclopropyl)-1-ethyl;

R 2 is chloro or trifluoromethyl;

R 3 is hydrogen, chloro or fluoro;

X is O; and

Ar is pyridinyl substituted with at least one methyl, or phenyl substituted with COOH or hydroxyC 1-3 alkyl;

or a pharmaceutically acceptable salt or a solvate thereof.

3. The method according to claim 1 wherein

R 1 is 1-butyl, 3-methyl-1-butyl, (cyclopropyl)methyl or 2-(cyclopropyl)-1-ethyl;

R 2 is chloro;

R 3 is chloro or fluoro;

X is O; and

Ar is 2-methylpyridin-4-yl, 2-methylpyridin-3-yl or 2,6-dimethylpyridin-4-yl,

or a pharmaceutically acceptable salt thereof.

4. The method according to claim 1 wherein said compound is selected from the group consisting of:

1-Butyl-3-chloro-4-[4-(2-methylpyridin-4-yloxy)-phenyl]-1H-pyridin-2-one

1-Butyl-3-chloro-4-[2-fluoro-4-(2-methylpyridin-4-yloxy)-phenyl]-1H-pyridin-2-one

3-Chloro-1-cyclopropylmethyl-4-[4-(2,6-dimethylpyridin-3-yloxy)-3-fluoro-phenyl]-1H-pyridin-2-one

4-[4-(1-Butyl-3-chloro-2-oxo-1,2-dihydro-pyridin-4-yl)-phenoxy]-benzoic acid

1-Cyclopropylmethyl-4-[4-(2,6-dimethyl-pyridin-4-yloxy)-3-fluoro-phenyl]-3-trifluoromethyl-1H-pyridin-2-one.

5. The method of claim 1 , wherein the central nervous system disorder is an anxiety disorder selected from the group consisting of agoraphobia, generalized anxiety disorder (GAD), obsessive-compulsive disorder (OCD), panic disorder, posttraumatic stress disorder (PTSD), social phobia and other phobias.

6. The method of claim 1 , wherein the central nervous system disorder is a psychotic disorder selected from the group consisting of schizophrenia, schizoaffective disorder, and schizophreniform disorder.

7. The method of claim 1 , wherein the central nervous system disorder is a mood disorder selected from the group consisting of bipolar disorders (I & II), cyclothymic disorder, depression, dysthymic disorder, major depressive disorder and substance-induced mood disorder.

8. The method of claim 1 , wherein the central nervous system disorder is epilepsy or a convulsive disorder selected from the group consisting of generalized nonconvulsive epilepsy, generalized convulsive epilepsy, petit mal status epilepticus, grand mal status epilepticus, partial epilepsy with or without impairment of consciousness, infantile spasms, epilepsy partialis continua, and other forms of epilepsy.

9. The method of claim 1 , wherein the central nervous system disorder is selected from the group consisting of anxiety, schizophrenia, depression, and epilepsy.

10. The method of claim 1 , further comprising administering an orthosteric agonist of mGluR2 in combination with the compound of formula (I).

11. The method of claim 1 , wherein the central nervous system disorder is dementia of the Alzheimer's type.

12. The method of claim 9 , wherein the central nervous system disorder is anxiety.

13. The method of claim 9 , wherein the central nervous system disorder is schizophrenia.

14. The method of claim 9 , wherein the central nervous system disorder is depression.

15. The method of claim 9 , wherein the central nervous system disorder is epilepsy.

Assignments (1)
CHANGE OF NAME Recorded Nov 4, 2013
From: ADDEX PHARMACEUTICALS SA
To: ADDEX PHARMA SA
Reel/Frame 031573/0380 →
Priority Claims (1)
EP 07116388 · Sep 14, 2007 · regional
Continuity (2)
Division 12677691
Related Publication 20120309793A1 · Dec 6, 2012