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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
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-87
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-24
filingDate 2001-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bcdefeccbb19703e609c591b5f35f7d9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fab9bd5f2956a73ab96a12ae41662b6c
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publicationDate 2001-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NL-1018360-C1
titleOfInvention Process for the preparation of pure Citalopram.
abstract Preparation of citalopram involves removal of the desmethyl-citalopram impurity by reaction with an amide or an amide-like group forming agent; removing the amides, and further purifying the crude product to isolate the base citalopram. Preparation of citalopram (I) by subjecting a compound of formula (II) to a cyanide exchange reaction with a cyanide source involves: optionally subjecting the resultant crude (I) to initial purification; subsequently treating with an amide or an amide-like group forming agent (a) R-CO-X; Hal-C(Y')-W'-R or R'-SO2-Hal; subjecting the reaction mixture to an acid/base wash and/or crystallization and recrystallization to remove the amides formed from the crude mixture; optionally purifying the resulting product of (I), working up and isolating (I) as a base or a salt. Z = I, Br, Cl, CF3-(CF2)nSO2-O-; n = 0 - 8; X = halogen or O-CO-R'; Y' = O or S; W' = O, N or S; and R, R', R and R' = H, alkyl or optionally substituted aryl or aralkyl.
priorityDate 2000-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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