http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8664389-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C257-12
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C257-12
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C251-00
filingDate 2009-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7374120a288aa2dd3c80e67afa0870c2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cc0a1ad634acb22e487b4f652c20ba30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_259eb40531859e401e262f1c88ac724b
publicationDate 2014-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8664389-B2
titleOfInvention Process for the preparation of lapatinib and it's pharmaceutically acceptable salts
abstract The present invention relates to an improved and novel process for the preparation of high purity crystalline base of Lapatinib of formula-(1) having chemical name N-{3-chloro-4-[(3-fluorobenzyloxy]phenyl}-6-[5-({[2-(methanesulfonyl)ethyl]amino}methyl]-2-furyl]-4-quin-azolinamine and its pharmaceutically acceptable salts. The present invention further relates to intermediates according to formula (8) and formula (9) used in this process.
priorityDate 2008-11-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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