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filingDate 1999-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3475e077e646945108ca42ac10d97d30
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publicationDate 2001-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1140910-A1
titleOfInvention Process for the preparation of an acetate salt of paroxetine or paroxetine analogues
abstract The present invention relates to a new process for the preparation of an acetate salt of a compound of formula (1) in which R1 is a substituted phenyl group, preferably 3,4-methylenedioxyphenyl; the process comprising treating a solution of the compound of formula (1) with acetic acid and a co-solvent. The (-) trans isomer of 4-(4'-fluorophenyl)-3-(3',4'-methylenedioxyphenoxymethyl)-piperidine (paroxetine) is an important compound having antidepressant and anti-Parkinson properties. This compound is used in therapy as the hydrochloride salt to treat inter alia depression obsessive compulsive disorder (OCD) and panic.
priorityDate 1998-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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