http://rdf.ncbi.nlm.nih.gov/pubchem/patent/NZ-521200-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-87
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-343
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-87
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-343
filingDate 2001-03-01^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b51128e00f2d46ac405f04d8383ff43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7694f7bfc6c576797858ab5eca314a97
publicationDate 2004-03-26^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-521200-A
titleOfInvention Method for the preparation of citalopram
abstract Disclosed is a method of preparing the antidepressant drug citalopram (1-[3-(dimethylamino)propyl]-1-(4- fluorophenyl)-1,3-dihydro-5-isobenzofurancarbonitrile) by reacting a compound of formula (II) with a compound of formula (III), wherein R is halogen or -O-SO2-X (X=alkyl, alkenyl) and R1 is dimethylamino, halogen or -O-SO2-X. Note if R1 is halogen or -O-SO2-X, then conversion of the resulting compound of said reaction will accordingly follow.
priorityDate 2000-03-03^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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