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filingDate 2000-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_262e2e3d5a4276ce6f01d39b122eb29a
publicationDate 2001-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-0104113-A2
titleOfInvention Process for the preparation of paroxetine and synthetic intermeditates thereof
abstract The present invention relates to a new process for preparing pharmaceutically active compounds and intermediates therefor. 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. There is described herein an improved process for its preparation which avoids several isolation and purification steps required in the prior art.
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