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filingDate 2007-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e281536d0b4fc5374dfb2d4e10ab0d3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_86f298c66882cff926861cd940ead4a4
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publicationDate 2014-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2492645-T3
titleOfInvention An improved procedure for the preparation of erlotinib hydrochloride
abstract A process for the preparation of erlotinib substantially free of N-methoxyethyl impurity, namely N- [(3-ethynylphenyl) - (2-methoxyethyl)] - 6,7-bis (2-methoxyethoxy) -4-quinazolinamine, or a of its pharmaceutically acceptable salts, which comprises isolating erlotinib or a pharmaceutically acceptable salt of erlotinib from a solvent medium comprising dimethylsulfoxide and an alcoholic solvent.
priorityDate 2007-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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