http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007516163-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-85
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-85
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-04
filingDate 2004-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2007-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2007516163-A
titleOfInvention Method for preparing 3-aminothienopyridone derivative
abstract The present invention relates to 3-amino-7H-thieno [2,3-b] pyridine substituted with an aryl, heteroaryl, cycloalkyl or heterocycloalkyl group at the 7-position and a specific range of substituents at the 2-position. A class of -6-one derivatives is provided; methods for preparing these compounds and their use as intermediates in the manufacture of certain p38 MAP kinase inhibitors are also provided.
priorityDate 2003-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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