IP Library Granted Patent US 9,233,934
Granted Patent B2
US 9,233,934 · App. 13/913,369 · Granted Jan 12, 2016

Phenyl amino pyrimidine compounds and uses thereof

Inventors: Christopher John Burns (Richmond, AU); Andrew Craig Donohue (Richmond, AU); John Thomas Feutrill (Richmond, AU); Thao Lien Thi Nguyen (Richmond, AU); Andrew Frederick Wilks (Richmond, AU); Jun Zeng (Richmond, AU)
Assignee: YM BIOSCIENCES AUSTRALIA PTY LTD
C07D239/42C07D295/02C07D295/12C07D401/12C07D401/14C07D403/12C07D405/12C07D417/12
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Quick Facts
Patent No.
US 9,233,934
App. No.
13/913,369
Granted
Jan 12, 2016
Kind
B2
Abstract

The present invention relates to phenyl amino pyrimidine compounds which are inhibitors of protein kinases including JAK kinases. In particular the compounds are selective for JAK2 kinases. The kinase inhibitors can be used in the treatment of kinase associated diseases such as immunological and inflammatory diseases including organ transplants; hyperproliferative diseases including cancer and myeloproliferative diseases; viral diseases; metabolic diseases; and vascular diseases.

Claims (39)

1. A compound selected from the group consisting of:

N-(2-cyanopropan-2-yl)-4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)benzamide;

N-(cyanomethyl)-4-(2-(3-morpholinophenylamino)pyrimidin-4-yl)benzamide;

N-(cyanomethyl)-4-(2-(4-thiomorpholinophenylamino)pyrimidin-4-yl)benzamide;

N-(cyanomethyl)-4-(2-(4-iodophenylamino)pyrimidin-4-yl)benzamide;

N-(cyanomethyl)-N-(4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)phenyl)methanesulfonamide;

N-(cyanomethyl)-4-(2-(4-(morpholinomethyl)phenylamino)pyrimidin-4-yl)benzamide;

N-(2-(cyanomethylamino)-2-oxoethyl)-4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)benzamide;

N-(cyanomethyl)-4-(2-(4-(4-hydroxypiperidin-1-yl)phenylamino)pyrimidin-4-yl)benzamide;

N-(cyanomethyl)-4-(2-(4-(4-methylpiperazin-1-yl)phenylamino)pyrimidin-4-yl)benzamide;

N-(cyanomethyl)-4-(2-(4-(3-hydroxypiperidin-1-yl)phenylamino)-5-methylpyrimidin-4-yl)benzamide;

4-(2-(4-(1-benzylpiperidin-4-yloxy)phenylamino)pyrimidin-4-yl)-N-(cyanomethyl)benzamide;

N-(cyanomethyl)-4-(2-(6-morpholinopyridin-3-ylamino)pyrimidin-4-yl)benzamide;

4-(2-(4-(4-acetylpiperazin-1-yl)phenylamino)pyrimidin-4-yl-(cyanomethyl)benzamide;

N-(4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)phenyl)-N-(prop-2-ynyl)methanesulfonamide tosylate;

N-(cyanomethyl)-4-(2-(4-(piperidin-4-yloxy)phenylamino)pyrimidin-4-yl)benzamide;

5-(4-(4-(cyanomethylcarbamoyl)phenyl)pyrimidin-2-ylamino)-N,N-dimethyl-2-morpholinobenzamide;

N-tert-butyl-5-(4-(4-(cyanomethylcarbamoyl)phenyl)pyrimidin-2-ylamino)-2-morpholinobenzamide;

5-(4-(4-(cyanomethylcarbamoyl)phenyl)pyrimidin-2-ylamino)-N-ethyl-2-morpholinobenzamide;

N-(cyanomethyl)-4-(2-(3-fluoro-4-morpholinophenylamino)pyrimidin-4-yl)benzamide;

N-(cyanomethyl)-4-(2-(4-morpholino-3-(trifluoromethyl)phenylamino)pyrimidin-4-yl)benzamide;

5-(4-(4-(N-(cyanomethyl)methylsulfonamido)phenyl)pyrimidin-2-ylamino)-N-(2-(dimethylamino)ethyl)-2-morpholinobenzamide;

N-(cyanomethyl)-N-(4-(2-(4-morpholino-3-(trifluoromethyl)phenylamino) pyrimidin-4-yl)phenyl)methanesulfonamide;

N-(cyanomethyl)-4-(2-(3-(propoxymethyl)phenylamino)pyrimidin-4-yl)benzamide;

4-(2-(3-(allyloxymethyl)-4-morpholinophenylamino)pyrimidin-4-yl)-N-(cyanomethy)benzamide;

N-(cyanomethyl)-4-(2-(4-(1-ethylpiperidin-4-yloxy)phenylamino)pyrimidin-4-yl)benzamide;

N-(cyanomethyl)-N-(4-(2-(3-fluoro-4-morpholinophenylamino)pyrimidin-4-yl)phenyl)methanesulfonamide;

N-(4-(2-(3-cyano-4-morpholinophenylamino)pyrimidin-4-yl)phenyl)-N-(cyanomethyl)methanesulfonamide;

2-cyano-N-(4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)phenyl)acetamide;

N-(cyanomethyl)-4-(2-(4-(2-morpholinoethoxy)phenylamino)pyrimidin-4-yl)benzamide;

N-(cyanomethyl)-4-(2-{[4-(1,1-dioxo-1λ 6 ,4-thiomorpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzamide;

N-(cyanomethyl)-4-[2-({4-[(1,1-dioxo-1 λ 6 ,4-thiomorpholin-4-yl)methyl]phenyl}amino)pyrimidin-4-yl]benzamide;

N-(cyanomethyl)-N-methyl-4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)benzamide; and

N-(cyanomethyl)-4-(5-methyl-2-(4-morpholinophenylamino)pyrimidin-4-yl)benzamide;

or a pharmaceutically acceptable salts thereof.

2. A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.

3. A method for the treatment of a Janus kinase associated disease which comprises administering to a subject in need an effective amount of the compound of claim 1 or a pharmaceutical composition thereof.

4. The method of claim 3 , wherein the disease is a myeloproliferative disease selected from the group consisting of myelofibrosis, polycythemia vera (PV), and essential thrombacythemia (ET).

5. A method of inhibiting a Janus kinase in a cell comprising contacting the cell with the compound of claim 1 .

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 7, 2023
From: SIERRA ONCOLOGY LLC
To: GLAXOSMITHKLINE LLC
Reel/Frame 063879/0821 →
CHANGE OF NAME Recorded May 26, 2023
From: SIERRA ONCOLOGY, INC.
To: SIERRA ONCOLOGY LLC
Reel/Frame 063790/0568 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 3, 2018
From: YM BIOSCIENCES AUSTRALIA PTY LTD
To: SIERRA ONCOLOGY, INC.
Reel/Frame 047059/0834 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2014
From: BURNS, CHRISTOPHER JOHN; DONOHUE, ANDREW CRAIG; FEUTRILL, JOHN THOMAS; NGUYEN, THAO LIEN THI; WILKS, ANDREW FREDERICK; ZENG, JUN
To: CYTOPIA RESEARCH PTY LTD
Reel/Frame 032110/0295 →
CHANGE OF NAME Recorded Jan 31, 2014
From: CYTOPIA RESEARCH PTY LTD
To: YM BIOSCIENCES AUSTRALIA PTY LTD
Reel/Frame 032149/0903 →
Continuity (4)
Continuation 12530610
Provisional Application 60894264 · Mar 12, 2007
Provisional Application 61016252 · Dec 21, 2007
Related Publication 20140005180A1 · Jan 2, 2014