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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D451-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D451-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D451-02
filingDate 2008-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7e809952f98665a2f71168bc6051c8ab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d14c2b76fdb64322a0f949ff4c208886
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a688115c62081775c75a54f4162e9806
publicationDate 2015-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2690606-C
titleOfInvention Process for preparing an intermediate to mu opioid receptor antagonists
abstract The invention provides an efficient method for preparing 3-endo-(S-azabicyclo[3.2.1]oct-3-yl)benzamide by hydrogenation, under controlled conditions, of an amino-protected 3-(8-azabicyclo[3.2.1]oct-2-en-3-yl)benzamide intermediate in which the amino-protecting group is removable by catalytic hydrogenation.
priorityDate 2007-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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