IP Library Granted Patent US 9,737,534
Granted Patent B2
US 9,737,534 · App. 14/840,118 · Granted Aug 22, 2017

Oxazoline and isoxazoline derivatives as CRAC modulators

Inventors: Nageswara Rao Irlapati (Maharashtra, IN); Gokul Keruji Deshmukh (Maharashtra, IN); Vijay Pandurang Karche (Maharashtra, IN); Santosh Madhukar Jachak (Maharashtra, IN); Neelima Sinha (Maharashtra, IN); Venkata P. Palle (Maharashtra, IN); Rajender Kumar Kamboj (Maharashtra, IN)
Assignee: LUPIN LIMITED
A61K31/497A61K31/42A61K31/421A61K31/422A61K31/423A61K31/4245A61K31/433A61K31/4439A61K31/496C07D261/12C07D413/10C07D413/14C07D417/14
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Quick Facts
Patent No.
US 9,737,534
App. No.
14/840,118
Granted
Aug 22, 2017
Kind
B2
Abstract

The present invention relates to compounds of Formula (I), along with processes for their preparation that are useful for treating, preventing and/or managing the diseases, disorders, syndromes or conditions associated with the modulation of CRAC. The invention further relates to methods of treating, preventing managing and/or lessening the diseases, disorders, syndromes or conditions associated with the modulation of CRAC of Formula (I).

Claims (52)

1. A method of treating rheumatoid arthritis in a subject in need thereof, wherein the method comprises administering to the subject a therapeutically effective amount of a compound of Formula (I):

wherein:

R 1 , which may be same or different at each occurrence, is independently selected from halogen, alkyl, haloalkyl, alkoxy and cycloalkyl;

R 2 is selected from hydrogen, halogen, hydroxyl, alkyl, haloalkyl, alkoxy, haloalkoxy, and cycloalkyl;

R is alkyl; and

p is an integer ranging from 0 to 2, both inclusive;

or a pharmaceutically acceptable salt thereof or stereoisomers thereof.

2. The method of claim 1 , wherein the method comprises administering to the subject a therapeutically effective amount of a compound selected from:

2,6-Difluoro-N-(2′-methyl-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

N-(5′-(4-Ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2′-methyl-[1,1′-biphenyl]-4-yl)-2,6-difluorobenzamide,

2,6-Difluoro-N-(2′-methyl-5′-(5-oxo-4-propyl-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

N-(2′-Ethyl-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-2,6-difluorobenzamide,

2-Chloro-N-(2′-ethyl-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-6-fluorobenzamide,

N-(2′-Ethyl-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-2-fluoro-6-methylbenzamide,

2,6-Difluoro-N-(2′-methoxy-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

2-Chloro-6-fluoro-N-(2′-methoxy-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

2-Fluoro-N-(2′-methoxy-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-6-methylbenzamide,

4-Ethyl-N-(2′-methoxy-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

N-(2′-(Difluoromethoxy)-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-2,6-difluorobenzamide,

N-(2′-Chloro-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-2,6-difluorobenzamide,

2,6-Difluoro-N-(2′-methyl-3′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

2-Chloro-6-fluoro-N-(2′-methyl-3′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

N-(2′-ethyl-3′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-2,6-difluorobenzamide,

or pharmaceutically acceptable salt thereof.

3. A method of treating rheumatoid arthritis in a subject in need thereof, wherein the method comprises administering to the subject a therapeutically effective amount of a compound which is 2,6-Difluoro-N-(2′-methyl-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide.

4. A method of treating rheumatoid arthritis in a subject in need thereof, wherein the method comprises administering to the subject a therapeutically effective amount of a compound which is N-(5′-(4-Ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2′-methyl-[1,1′-biphenyl]-4-yl)-2,6-difluorobenzamide.

5. A method of treating rheumatoid arthritis in a subject in need thereof, wherein the method comprises administering to the subject a therapeutically effective amount of a compound which is 2,6-Difluoro-N-(2′-methyl-3′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide.

6. A method of treating rheumatoid arthritis in a subject in need thereof, wherein the method comprises administering to the subject a therapeutically effective amount of a compound which is 2-Chloro-6-fluoro-N-(2′-methyl-3′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide.

7. A method of treating rheumatoid arthritis in a subject in need thereof, wherein the method comprises administering to the subject a pharmaceutical composition comprising a compound of Formula (I):

wherein:

R 1 , which may be same or different at each occurrence, is independently selected from halogen, alkyl, haloalkyl, alkoxy and cycloalkyl;

R 2 is selected from hydrogen, halogen, hydroxyl, alkyl, haloalkyl, alkoxy, haloalkoxy, and cycloalkyl;

R is alkyl; and

p is an integer ranging from 0 to 2, both inclusive;

or a pharmaceutically acceptable salt thereof or stereoisomers thereof.

8. A method of treating rheumatoid arthritis in a subject in need thereof, wherein the method comprises administering to the subject a pharmaceutical composition comprising a compound selected from:

2,6-Difluoro-N-(2′-methyl-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

N-(5′-(4-Ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2′-methyl-[1,1′-biphenyl]-4-yl)-2,6-difluorobenzamide,

2,6-Difluoro-N-(2′-methyl-5′-(5-oxo-4-propyl-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

N-(2′-Ethyl-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-2,6-difluorobenzamide,

2-Chloro-N-(2′-ethyl-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-6-fluorobenzamide,

N-(2′-Ethyl-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-2-fluoro-6-methylbenzamide,

2,6-Difluoro-N-(2′-methoxy-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

2-Chloro-6-fluoro-N-(2′-methoxy-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

2-Fluoro-N-(2′-methoxy-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-6-methylbenzamide,

4-Ethyl-N-(2′-methoxy-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

N-(2′-(Difluoromethoxy)-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-2,6-difluorobenzamide,

N-(2′-Chloro-5′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-2,6-difluorobenzamide,

2,6-Difluoro-N-(2′-methyl-3′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

2-Chloro-6-fluoro-N-(2′-methyl-3′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide,

and N-(2′-ethyl-3′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)-2,6-difluorobenzamide,

or a pharmaceutically acceptable salt thereof.

Assignments (1)
CHANGE OF ADDRESS Recorded Jan 27, 2017
From: LUPIN LIMITED
To: LUPIN LIMITED
Reel/Frame 041936/0001 →
Priority Claims (2)
IN 1215/KOL/2010 · Oct 30, 2010 · national
IN 473/KOL/2011 · Apr 1, 2011 · national
Continuity (2)
Division 13882567
Related Publication 20160022673A1 · Jan 28, 2016