http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006293530-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C215-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-87
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-02
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-00
filingDate 2006-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6350324b40041ca970ce355e4e5f1aea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b7417d03d7fef1861532645f3a854ce
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publicationDate 2006-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2006293530-A1
titleOfInvention Process for the manufacture of citalopram hydrobromide
abstract The present invention describes an improved process for the preparation of pure 1-(4′-Fluorophenyl)-1-(3-dimethylaminopropyl)-5-phthalanecarbonitrile and its bromide salt (citalopram hydrobromide), which is a well known antidepressant. Another aspect of the invention is isolation of crystalline (4-Bromo-2-hydroxymethyl)phenyl-(4-fluorophenyl)-3-(dimethylaminopropyl)methanol (Bromodiol) and conversion of desmethylcitalopram which is formed during the cyanide exchange reaction, to citalopram by heating with a mixture of formaldehyde and formic acid in chloroform. The resulting citalopram is purified using conventionally extraction methodology.
priorityDate 2003-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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