http://rdf.ncbi.nlm.nih.gov/pubchem/patent/MX-PA05008411-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_257e52a8fcb6658dc74983b64fd511b7
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-87
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-24
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-87
filingDate 2004-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72dc649bd0797343f2beb3984064e4be
publicationDate 2005-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber MX-PA05008411-A
titleOfInvention PROCEDURE FOR THE PREPARATION OF A CIANOISOBENZOFURAN.
abstract A process for the preparation of citalopran and the pharmaceutically acceptable salts thereof is described, by reacting 5-cyanophthalide with a 4-fluorophenylmagnesium halide, reducing 3-hydroxymethyl-4 (4-fluorobenzoyl) benzonitrile with a ketone reducing agent. To alcohols, send 3-hydroxymethyl-4 - [(4-fluorophenyl) hydroxymethyl) benzonitrile obtained in this way to a cyclization reaction to provide 1- (4-fluorophenyl) -1,3-dihydro-5-isobenzofurannocarbonitrile without 1 , 1-bis (4-fluorophenyl) -1,3-dihydro-5-isobenzofurancarbonitrile and treat 1,1-bis (4-fluorophenyl) -1,3-dihydro-5-isobenzofurannocarbonitrile with a 3- (dimethylamino) halide ) propyl in the presence of a base.
priorityDate 2003-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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