http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2007731-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d202e9e866984fe229f6facc38f1d740
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D223-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D223-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55
filingDate 2007-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39a0cd34c8e877db1898a00335ef0f2f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a134dc125254d006b5deddf983baa385
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_92e4a6694067f1ee9ca3299699eaa4b9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_258ed0764c7a5a37b0f27c8d6707f2cb
publicationDate 2009-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2007731-B1
titleOfInvention Process for the preparation of caprolactam cgrp antagonist intermediate
abstract An efficient syntheses for the preparation of (3R,6S)-3-amino-6-(2,3- difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one. The process uses a crystallization driven asymmetric transformation to set the amine stereocenter followed by a cis-selective hydrogenation and epimerization to set the benzylic stereocenter and trans geometry.
priorityDate 2006-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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