Abstract: The invention relates to processes for preparing compounds having the formula, and crystalline forms thereof, wherein Ar is aryl or heteroaryl, L is an optional alkylene linker, and R2, R3, R4, and R5, are as defined in the specification herein, which compounds are useful as kinase inhibitors, in particular, inhibitors of protein tyrosine kinase and p38 kinase.
Type:
Grant
Filed:
December 23, 2008
Date of Patent:
August 14, 2012
Assignee:
Bristol-Myers Squibb Company
Inventors:
Jean Lajeunesse, John D. DiMarco, Michael Galella, Ramakrishnan Chidambaram
Abstract: The present invention provides for tricyclic compounds having the formula (I), wherein R1, R2, R5, R6, R7, and R8 are as described herein. The present invention further provides pharmaceutical compositions comprising such compounds, as well as the use of such compounds for treating inflammatory and immune diseases.
Type:
Grant
Filed:
May 8, 2006
Date of Patent:
June 15, 2010
Assignee:
Bristol-Myers Squibb Company
Inventors:
William J. Pitts, James Kempson, Junqing Guo, Jagabandhu Das, Charles M. Langevine, Steven H. Spergel, Scott Hunter Watterson
Abstract: The present invention is directed to metabolites of ?N-(2-Chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino]-5-thiazolecarboxamide, the compound of formula (I), pharmaceutical compositions thereof, and to methods of using the metabolites and the pharmaceutical compositions in the treatment of oncological and immunological disorders.
Type:
Grant
Filed:
March 15, 2006
Date of Patent:
November 24, 2009
Assignee:
Bristol-Myers Squibb Company
Inventors:
Vinod Kumar Arora, Lisa Joy Christopher, Donghui Cui, Wenying Li
Abstract: The present invention provides for thiazolopyridine-based tricyclic compounds having the formula (I), wherein R1, R2, R5 and R6 are as described herein. The present invention further provides pharmaceutical compositions comprising such compounds, as well as the use of such compounds for treating inflammatory and immune diseases.
Type:
Grant
Filed:
November 10, 2005
Date of Patent:
July 7, 2009
Assignee:
Bristol-Myers Squibb Company
Inventors:
Jagabandhu Das, James Kempson, William J. Pitts, Steven H. Spergel
Abstract: The present application describes modulators of CCR3 of formula (I): A—E—NR1—G??(I) or pharmaceutically acceptable salt forms thereof, useful for the prevention of inflammatory diseases such as asthma and other allergic diseases.
Type:
Grant
Filed:
September 13, 2005
Date of Patent:
June 23, 2009
Assignee:
Bristol-Myers Squibb Company
Inventors:
John V Duncia, Joseph B Santella, III, Daniel S Gardner, Dean A Wacker
Abstract: The present application describes modulators of chemokine receptor activity of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma and other allergic diseases, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis, including methods of preparing and intermediates thereof.
Abstract: The present application describes a process of preparing a compound of formula (IV), or salt or stereoisomer thereof: wherein Pg, at each occurrence, is independently selected from an amine protecting group; comprising the steps of reacting a compound of Formula with a reducing agent to give a compound of Formula III: reacting the compound of formula (III) with an amine of formula (IIa) using reductive amination to give the compound of formula (III)
Abstract: The present application describes modulators of CCR3 of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma and other allergic diseases.
Abstract: The invention relates to processes for preparing compounds having the formula, and crystalline forms thereof, wherein Ar is aryl or heteroaryl, L is an optional alkylene linker, and R2, R3, R4, and R5, are as defined in the specification herein, which compounds are useful as kinase inhibitors, in particular, inhibitors of protein tyrosine kinase and p38 kinase.
Type:
Grant
Filed:
July 29, 2005
Date of Patent:
February 17, 2009
Assignee:
Bristol-Myers Squibb Company
Inventors:
Jean Lajeunesse, John D. DiMarco, Michael Galella, Ramakrishnan Chidambaram
Abstract: The present application describes modulators of chemokine receptor activity of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma and other allergic diseases, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis, including methods of preparing and intermediates thereof.
Abstract: The present invention provides for pyrazolopurine-based tricyclic compounds having the formula (I), wherein R1, R2, R3, R4, R5 and R6 are as described herein. The present invention further provides pharmaceutical compositions comprising such compounds, as well as the use of such compounds for treating inflammatory and immune diseases.
Type:
Grant
Filed:
February 24, 2004
Date of Patent:
February 12, 2008
Assignee:
Bristol-Myers Squibb Company
Inventors:
Yuping Qiu, Makonen Belema, Xuejie Yang, Fred Christopher Zusi, William J. Pitts
Abstract: The present application describes modulators of CCR3 of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma and other allergic diseases.
Type:
Grant
Filed:
March 25, 2004
Date of Patent:
December 25, 2007
Assignee:
Bristol-Myers Squibb Pharma Company
Inventors:
Soo S. Ko, George V. Delucca, John V. Duncia, Joseph B. Santella, III, Dean A. Wacker
Abstract: The present application describes modulators of chemokine receptors of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma and other allergic diseases.
Type:
Grant
Filed:
November 12, 2004
Date of Patent:
November 6, 2007
Assignee:
Bristol-Myers Squibb Company
Inventors:
Soo S. Ko, Douglas G. Batt, George V. Delucca, John V. Duncia, Daniel S. Gardner, Joseph B. Santella
Abstract: The present invention provides novel methods for the synthesis of (S)-6-chloro-4-cyclopropylethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one of formula (III) which is useful as a human immunodeficiency virus (HIV) reverse transcriptase inhibitor.
Type:
Grant
Filed:
September 1, 2005
Date of Patent:
April 17, 2007
Assignee:
Bristol-Myers Squibb Company
Inventors:
Purushotham Vemishetti, Scott T. Chadwick, Carrie A. Costello, Sridhar Desikan, Emily A. Reiff
Abstract: Novel cyclic compounds and salts thereof, pharmaceutical compositions containing such compounds, and methods of using such compounds in the treatment of protein tyrosine kinase-associated disorders such as immunologic and oncologic disorders.
Type:
Grant
Filed:
May 26, 2005
Date of Patent:
March 13, 2007
Assignee:
Bristol-Myers Squibb Company
Inventors:
Jagabandhu Das, Ping Chen, Derek J. Norris
Abstract: The present application describes modulators of MCP-1 of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the prevention of rheumatoid arthritis, multiple sclerosis, atherosclerosis and asthma, processes for preparing and intermediates thereof.
Type:
Grant
Filed:
February 11, 2004
Date of Patent:
February 27, 2007
Assignee:
Bristol-Myers Squibb Company
Inventors:
Robert J. Cherney, Percy H. Carter, John V. Duncia, Daniel S. Gardner, Joseph B. Santella
Abstract: The present invention provides for pyrazolopurine-based tricyclic compounds having the formula (I), wherein R1, R2, R3, R4, R5 and R6 are as described herein. The present invention further provides pharmaceutical compositions comprising such compounds, as well as the use of such compounds for treating inflammatory and immune diseases.
Type:
Grant
Filed:
May 18, 2004
Date of Patent:
February 13, 2007
Assignee:
Bristol-Myers Squibb Company
Inventors:
William J. Pitts, Makonen Belema, Patrice Gill, James Kempson, Yuping Qiu, Claude A. Quesnelle, Steven H. Spergel, Fred Christopher Zusi