http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2516370-C

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-02
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-506
filingDate 2004-01-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f44b88f795e587053ca53040cb30f49f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e13f5514fa42ebfb804c3bcc5c58a4d
publicationDate 2012-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2516370-C
titleOfInvention A process of preparing imatinib and imatinib prepared thereby
abstract A process of preparing imatinib, either as the free base or as an acid addition salt, which process comprises reacting N-(2-methyl-5-aminophenyl-4-(3-pyridyl)-2-pyrimidine amine of formula (II) with a 4-(4-methyl-piperazino methyl)benzoyl halide of formula (III) in the presence of an inert organic solvent, so as to yield a hydrohalide salt of imatini formula (I) where n represents 1, 2 or 3 and Hal represents bromo, chloro fluoro or iodo, either in anhydrous or hydrated form, which can as desired optionally be further conve either to the free base or a further acid addition salt. The present invention is also concerned with imatinib prepared according to the above process.
priorityDate 2003-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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