IP Library Patent Application 12246918
Patent Application
App. No. 12/246,918

2,6-SUBSTITUTED-4-MONOSUBSTITUTED AMINO-PYRIMIDINE AS PROSTAGLANDIN D2 RECEPTOR ANTAGONISTS

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Patent No.
US None
App. No.
12/246,918
Abstract

The present invention is directed to a compound of formula (I), wherein R 1 and R 2 are as defined herein, a pharmaceutical composition comprising a pharmaceutically effective amount of one or more compounds of the invention in admixture with a pharmaceutically acceptable carrier, and a method of treating a patient suffering from a PGD2-mediated disorder by administering to said patient a pharmaceutically effective amount of a compound of the invention.

Claims (74)

1 . A compound of formula (I):

wherein:

R 1 is 2,4-dichloro-phenyl or 4-trifluoromethoxy-phenyl, and

when R 1 is 2,4-dichloro-phenyl, then R 2 is 3-carboxy-pyrrolidinyl, 3,5-di-(1-hydroxy-1-methyl-ethyl)-phenyl, 3-amino-piperidin-1-yl, 4-amino-piperidin-1-yl, 4-acetamide-piperidin-1-yl, 1-methyl-2-carboxy-2,3-dihydro-1H-indol-5-yl, 3-(1-tert-butylsulfonylaminocarbonyl-1-methyl-ethyl)-phenyl, 3-(1-dimethylaminosulfonylaminocarbonyl-1-methyl-ethyl)-phenyl, 3-(1-thiomorpholin-4-ylcarbonyl-1-methyl-ethyl)-phenyl, 3-(1-aminocarbonyl-1-methyl-ethyl)-phenyl, 3-(1-dimethylaminocarbonyl-1-methyl-ethyl)-phenyl, 3-carboxymethyl-piperidin-1-yl, 3-methylsulfonylaminocarbonyl-piperidin-1-yl, 3-ethylsulfonylaminocarbonyl-piperidin-1-yl, 3-tert-butylsulfonylaminocarbonyl-piperidin-1-yl, 3-trifluoromethylsulfonylaminocarbonyl-piperidin-1-yl, 3-[(1H-tetrazol-5-yl)-aminocarbonyl]-piperidin-1-yl, 3-aminocarbonyl-piperidin-1-yl, 3-dimethylaminocarbonyl-piperidin-1-yl, 3-dimethylaminosulfonylaminocarbonyl-piperidin-1-yl, or 2-carboxy-2,3-dihydro-benzofuran-5-yl, and

when R 1 is 4-trifluoromethoxy-phenyl, then R 2 is 3-(1-methyl-1-carboxy-ethyl)-piperidinyl, 3-carboxy-piperidinyl, 3-methylsulfonylaminocarbonyl-piperidin-1-yl, 5-carboxy-thiophen-2-yl,

or a pharmaceutically acceptable salt, hydrate, or solvate thereof, a pharmaceutically acceptable prodrug thereof, or a pharmaceutically acceptable salt, hydrate or solvate of the prodrug.

2 . The compound according to claim 1 , which is

1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methyl-pyrimidin-4-yl}-pyrrolidine-3-carboxylic acid,

2-(1-{2-Methoxy-6-[2-(4-trifluoromethoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-piperidin-3-yl)-2-methyl-propionic acid,

2-[3-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-5-(1-hydroxy-1-methyl-ethyl)-phenyl]-propan-2-ol,

[6-(3-Amino-piperidin-1-yl)-2-methoxy-pyrimidin-4-yl]-[2-(2,4-dichloro-phenyl)-ethyl]-amine,

[6-(4-Amino-piperidin-1-yl)-2-methoxy-pyrimidin-4-yl]-[2-(2,4-dichloro-phenyl)-ethyl]-amine,

N-(1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidin-4-yl)-acetamide,

5-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-1-methyl-2,3-dihydro-1H-indole-2-carboxylic acid,

2-Methyl-propane-2-sulfonic acid [2-(3-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenyl)-2-methyl-propionyl]-amide,

N,N-dimethylamide-2-sulfonic acid [2-(3-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenyl)-2-methyl-propionyl]-amide,

2-(3-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenyl)-2-methyl-1-thiomorpholin-4-yl-propan-1-one,

2-(3-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenyl)-isobutyramide,

2-(3-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenyl)-N,N-dimethyl-isobutyramide,

(1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidin-3-yl)-acetic acid,

1-{2-Methoxy-6-[2-(4-trifluoromethoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-piperidine-3-carboxylic acid,

N-(1-{2-Methoxy-6-[2-(4-trifluoromethoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-piperidine-3-carbonyl)-methanesulfonamide,

N-(1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carbonyl)-methanesulfonamide,

Ethanesulfonic acid (1-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carbonyl)-amide,

2-Methyl-propane-2-sulfonic acid (1-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carbonyl)-amide,

N-(1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carbonyl)-C,C,C-trifluoro-methanesulfonamide,

1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carboxylic acid (1H-tetrazol-5-yl)-amide,

1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carboxylic acid amide,

1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carboxylic acid dimethylamide,

N,N-Dimethylamide-2-sulfonic acid 1-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carboxamide,

5-{2-Methoxy-6-[2-(4-trifluoromethoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-thiophene-2-carboxylic acid, or

5-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-2,3-dihydro-benzofuran-2-carboxylic acid.

3 . The compound or the ester prodrug according to claim 1 , which is

1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methyl-pyrimidin-4-yl}-pyrrolidine-3-carboxylic acid,

2-(1-{2-Methoxy-6-[2-(4-trifluoromethoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-piperidin-3-yl)-2-methyl-propionic acid,

2-[3-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-5-(1-hydroxy-1-methyl-ethyl)-phenyl]-propan-2-ol,

[6-(3-Amino-piperidin-1-yl)-2-methoxy-pyrimidin-4-yl]-[2-(2,4-dichloro-phenyl)-ethyl]-amine,

[6-(4-Amino-piperidin-1-yl)-2-methoxy-pyrimidin-4-yl]-[2-(2,4-dichloro-phenyl)-ethyl]-amine,

N-(1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidin-4-yl)-acetamide,

5-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-1-methyl-2,3-dihydro-1H-indole-2-carboxylic acid,

2-Methyl-propane-2-sulfonic acid [2-(3-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenyl)-2-methyl-propionyl]-amide,

N,N-dimethylamide-2-sulfonic acid [2-(3-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenyl)-2-methyl-propionyl]-amide,

2-(3-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenyl)-2-methyl-1-thiomorpholin-4-yl-propan-1-one,

2-(3-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenyl)-isobutyramide,

2-(3-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-phenyl)-N,N-dimethyl-isobutyramide,

(1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidin-3-yl)-acetic acid,

1-{2-Methoxy-6-[2-(4-trifluoromethoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-piperidine-3-carboxylic acid,

N-(1-{2-Methoxy-6-[2-(4-trifluoromethoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-piperidine-3-carbonyl)-methanesulfonamide,

5-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-1-methyl-2,3-dihydro-1H-indole-2-carboxylic acid ethyl ester,

(1-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidin-3-yl)-acetic acid ethyl ester,

N-(1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carbonyl)-methanesulfonamide,

Ethanesulfonic acid (1-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carbonyl)-amide,

2-Methyl-propane-2-sulfonic acid (1-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carbonyl)-amide,

N-(1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carbonyl)-C,C,C-trifluoro-methanesulfonamide,

1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carboxylic acid (1H-tetrazol-5-yl)-amide,

1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carboxylic acid amide,

1-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carboxylic acid dimethylamide,

N,N-Dimethylamide-2-sulfonic acid 1-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-piperidine-3-carboxamide,

5-{2-Methoxy-6-[2-(4-trifluoromethoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-thiophene-2-carboxylic acid, or

5-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yl}-2,3-dihydro-benzofuran-2-carboxylic acid,

or a pharmaceutically acceptable salt, hydrate, or solvate thereof.

4 . A pharmaceutical composition comprising a pharmaceutically effective amount of the compound according to claim 1 or a pharmaceutically acceptable salt, hydrate, or solvate thereof, a pharmaceutically acceptable prodrug thereof, or a pharmaceutically acceptable salt, hydrate or solvate of the prodrug, in admixture with a pharmaceutically acceptable carrier.

5 . A method for treating an allergic disease, systemic mastocytosis, a disorder accompanied by systemic mast cell activation, anaphylaxis shock, bronchoconstriction, bronchitis, urticaria, eczema, a diseases accompanied by itch, a disease which is generated secondarily as a result of behavior accompanied by itch, inflammation, chronic obstructive pulmonary diseases, ischemic reperfusion injury, cerebrovascular accident, chronic rheumatoid arthritis, pleurisy, or ulcerative colitis, in a patient in need thereof, comprising administering to the patient a pharmaceutically effective amount of the compound according to claim 1 , or a pharmaceutically acceptable salt, hydrate, or solvate thereof, a pharmaceutically acceptable prodrug thereof, or a pharmaceutically acceptable salt, hydrate or solvate of the prodrug.

6 . The method according to claim 5 , wherein the a disease which is generated secondarily as a result of behavior accompanied by itch is cataract, retinal detachment, inflammation, infection or sleeping disorder.

7 . The method according to claim 5 , wherein the allergic disease is allergic rhinitis, allergic conjunctivitis, atopic dermatitis, bronchial asthma or food allergy.

8 . The method according to claim 5 , wherein the disease accompanied by itch is atopic dermatitis or urticaria.

9 . The method according to claim 5 , wherein the disease that is generated secondarily as a result of behavior accompanied by itch is cataract, retinal detachment, inflammation, infection or sleeping disorder.

10 . The method according to claim 5 , which is for treating bronchial asthma.

11 . The method according to claim 5 , which is for treating allergic rhinitis.

12 . The method according to claim 5 , which is for treating allergic dermatitis.

13 . The method according to claim 5 , which is for treating allergic conjunctivitis.

14 . The method according to claim 5 , which is for treating chronic obstructive pulmonary disease.

15 . A pharmaceutical composition comprising a pharmaceutically effective amount of the compound according to claim 1 or a pharmaceutically acceptable salt, hydrate, or solvate thereof, a pharmaceutically acceptable prodrug thereof, or a pharmaceutically acceptable salt, hydrate or solvate of the prodrug, and a compound selected from the group consisting of an antihistamine, a leukotriene antagonist, a beta agonist, a PDE4 inhibitor, a TP antagonist and a CrTh2 antagonist, in admixture with a pharmaceutically acceptable carrier.

16 . The pharmaceutical composition according to claim 15 , wherein the antihistamine is fexofenadine, loratadine or citirizine, the leukotriene antagonist is montelukast or zafirlukast, the beta agonist is albuterol, salbuterol or terbutaline, the PDE4 inhibitor is roflumilast or cilomilast, the TP antagonist is Ramatroban, and the CrTh2 antagonist is Ramatroban.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2011
From: STEFANY, DAVID; HARRIS, KEITH JOHN; GILLESPY, TIMOTHY A.; GARDNER, CHARLES J.; AGUIAR, JOACY C.
To: SANOFI-AVENTIS U.S. LLC
Reel/Frame 026910/0007 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2011
From: SANOFI-AVENTIS U.S. LLC
To: SANOFI-AVENTIS
Reel/Frame 026912/0364 →
CHANGE OF NAME Recorded Sep 15, 2011
From: SANOFI-AVENTIS
To: SANOFI
Reel/Frame 026913/0092 →
CHANGE OF NAME Recorded Aug 2, 2011
From: SANOFI-AVENTIS
To: SANOFI
Reel/Frame 026686/0522 →