http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-112014007718-B1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_eb596f03d029321340c965e75de6564a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-94
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
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filingDate 2012-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da7bc85697709880fa3719b354e764d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73a10bb03aa4d14c57ae020c77fee6e5
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publicationDate 2022-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-112014007718-B1
titleOfInvention METHOD FOR PREPARING 1-(4-(4-(3,4-DICHLORO-2-FLUOROPHENYLAMINO)-7-METHOXYQUINAZOLIN-6-ILOXY)PIPERIDIN-1-IL)-PROP-2-EN-1-ONE E INTERMEDIARIES USED IN THE SAME
abstract method for preparing 1-(4-(4-(3,4-dichloro-2-fluorophenylamino)-7-methoxyquinazolin-6-yloxy)piperidin-1-yl)-prop-2-en-1-one hydrochloride and intermediaries used in it. the present invention relates to an improved method for preparing 1-(4-(4-(3,4-dichloro-2-fluorophenylamino)-7-methoxyquinazolin-6-yloxy)piperidin-1-yl)-prop-2 hydrochloride -en-1-one, which selectively and efficiently inhibits the development of cancer cells induced by overexpression of an epidermal development factor receptor (egfr) and prevents the development of drug resistance caused by a tyrosine kinase mutation , and intermediaries used in it.
priorityDate 2011-10-05-04:00^^<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: 20.