http://rdf.ncbi.nlm.nih.gov/pubchem/patent/IN-2014DN03447-A

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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_835e2293c5dcaba81155016ecfc87be3
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publicationDate 2015-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber IN-2014DN03447-A
abstract The present invention relates to an improved method for preparing l-(4-(4-(3,4-dichloro-2-fluorophenylamino)-7- methoxyquinazolin-6-yloxy)piperidin-l-yl)-prop-2-en-l-one hydrochloride, which selectively and effectively inhibits the growth of cancer cells induced by over-expression of an epidermal growth factor receptor (EGFR) and prevents the development of drug resistance caused by mutation of a tyrosine kinase, and intermediates used therein.
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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