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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12
filingDate 2015-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ce2cdeb10874d7c7ef03e927e515c02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_32c2691202afc6c87453d07f9842bc41
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f1ffe7e7ad6fda994e384b9182eb7529
publicationDate 2017-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-3224257-A1
titleOfInvention Novel method for preparing thienopyrimidine compound and intermediates used therein
abstract The present invention provides a novel method for preparing a thienopyrimidine compound of Formula 1, which is a selective inhibitor of tyrosine kinase activity, in particular, of mutant epidermal growth factor receptor tyrosine kinase, and novel intermediates used in the method.[ 1 ]
priorityDate 2014-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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