http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007191608-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-85
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-85
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-63
filingDate 2004-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f61add3825ad8fe3488ba68364095e35
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_87784bbfd218e5096961ba1fd25acb17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e218212bc2a98b5b540340ef092931ca
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c99107ed6b9bc36c9593e6000a3de638
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dc14caca3c6fe55d507cac95ac0b09ad
publicationDate 2007-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2007191608-A1
titleOfInvention Process for preparing 3-aminothienopyridone derivatives
abstract This invention provides a class of 3-amino-7H-thieno[2,3-b]pyridin-6-one derivatives, substituted in the 7-position by an aryl, heteroaryl, cycloalkyl or heterocycloalkyl moiety, and in the 2-position by a specified range of substituent groups; also provided is a process for preparing those compounds, and the use thereof as intermediates in the manufacture of certain p38 MAP kinase inhibitors.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2008319009-A1
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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Total number of triples: 819.