http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2008125578-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_53b7bcc9a398bb97e370a8dc5d24616f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b6042509de7544921c96de43b9da1438
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-14
filingDate 2008-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e8271789a731ff5e87ef7ba37f7d752
publicationDate 2008-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2008125578-A2
titleOfInvention A method for the preparation of mirtazapine
abstract The present invention relates to a method for the preparation of mirtazapine and tetracyclic analogous compounds having substantial enantiomeric excess of the R or S form. The invention further relates to a novel intermediate and its use for the preparation of mirtazapine having a substantial enantiomeric excess of the R or S form. The method comprising the steps of a: providing a carboxylic acid compound according to Formula (I) having a substantial enantiomeric excess of the R or S form, b: converting the carboxylic acid group of compound I into a ketone group, producing a ketone compound of Formula (II), c: optionally reducing ketone compound II with a mild reduction agent to form the intermediate hydroxy compound of Formula (III) and d: forming the mirtazapine of Formula (IV) by reduction of the ketone compound II or of the hydroxy compound III using a strong reduction agent.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-5952806-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2012133486-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9096523-B2
priorityDate 2007-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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