The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Apr. 14, 2020

Filed:

Jun. 23, 2016
Applicant:

Bristol-myers Squibb Company, Princeton, NJ (US);

Inventors:

John V. Duncia, Newtown, PA (US);

Daniel S. Gardner, Furlong, PA (US);

John Hynes, Washington Crossing, PA (US);

John E. Macor, Washington Crossing, PA (US);

Natesan Murugesan, Princeton Junction, NJ (US);

Joseph B. Santella, Springfield, PA (US);

Hong Wu, New Hope, PA (US);

Durgarao Kantheti, Bangalore, IN;

Satheesh Kesavan Nair, Bangalore, IN;

Venkatram Reddy Paidi, Bangalore, IN;

Sreekantha Ratna Kumar, Bangalore, IN;

Kandhasamy Sarkunam, Hosur, IN;

Ramesh Kumar Sistla, Bangalore, IN;

Subba Rao Polimera, Bangalore, IN;

Assignee:

Bristol-Myers Squibb Company, Princeton, NJ (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07D 487/04 (2006.01); C07D 401/14 (2006.01); C07D 413/04 (2006.01); C07D 471/04 (2006.01); A61P 29/00 (2006.01); A61P 11/00 (2006.01); A61P 1/00 (2006.01); A61P 25/04 (2006.01); A61P 19/02 (2006.01); A61P 37/06 (2006.01); A61P 11/06 (2006.01); A61P 17/06 (2006.01); A61P 37/00 (2006.01); A61P 35/00 (2006.01); A61K 31/519 (2006.01); A61K 31/435 (2006.01);
U.S. Cl.
CPC ...
C07D 487/04 (2013.01); C07D 401/14 (2013.01); C07D 413/04 (2013.01); C07D 471/04 (2013.01);
Abstract

Disclosed are compounds of Formula (I) Formula (I) or salts thereof, wherein HET is a heteroaryl selected from oxazolyl, pyrazolyl, imidazo[1,2-b]pyridazin-3-yl, and pyrazolo[1,5-a]pyrimidin-3-yl, wherein said heteroaryl is attached to the pyridinyl group in the compound of Formula (I) by a carbon ring atom in the heteroaryl and wherein said heteroaryl is substituted with zero to 2 R; and R, R, and Rare define herein. Also disclosed are methods of using such compounds as modulators of IRAK4, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing inflammatory and autoimmune diseases, or in the treatment of cancer.


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