http://rdf.ncbi.nlm.nih.gov/pubchem/patent/NZ-501285-A

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filingDate 1998-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eede432c502c6b75bfeed55757bef9cb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07776b8a82d17e4b5d3bc7be24f1e4f0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa6041ab2c87fdde91136199b022d934
publicationDate 2001-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-501285-A
titleOfInvention Process for preparing 4-(4'-fluorophenyl)-3-(3', 4'-methylenedioxy-phenyl)-piperidine
abstract Compounds of structure (1) are obtained by reduction of compounds of the structures (2a), (2b), (4a), (4b). Compounds of structure (1) in which R is hydrogen or an alkyl, aralkyl, aryl, acyl, alkoxycarbonyl, arylalkoxycarbonyl, aryloxycarbonyl group and especially where Z is a hydrogen atom or a 3,4-methylenedioxyphenyl group, are important intermediates for inter alia paroxetine. Disadvantages in the existing processes for preparation of such compounds are overcome, and so an alternative processes for their manufacture is provided. Paroxetine is the (-) trans isomer of 4-(4'fluorophenyl)-3-(3',4'-methylenedioxy-phenoxymethyl)-piperidine. This compound is used in therapy as the hydrochloride salt to treat inter alia depression, obsessive-compulsive disorder (OCD), Parkinson's disease and panic.
priorityDate 1997-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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