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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-10
filingDate 2006-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49d5949fb246607c44c714f57c4bdbf2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d80a29980296d07de6d4cf93d3786115
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_223889d5b68fbe727f2d43b0c3d20e1d
publicationDate 2009-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EA-012852-B1
titleOfInvention GETTING IRBESARTANA
abstract The present invention relates to a method for producing irbesartan or its pharmaceutically acceptable salts, including the synthesis of tritylrbesartan using the reaction of 5- (4- (bromomethyl) biphenyl-2-yl) -1- (triphenylmethyl) tetrazole and 2-n-butyl-4-cyclopentane -2-imidazolin-5-one or its salt in an organic solvent in the presence of a phase transfer catalyst and a base, removal of the protective group and isolation of irbesartan or its pharmaceutically acceptable salt.
priorityDate 2005-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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