http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004072866-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-445
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-445
filingDate 2002-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55a6d0fff165a517f4872e8ba82052d7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be148c1516a332aa3b3553e4c38716e9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e698ec54c5154215e57862f2c1a83c07
publicationDate 2004-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2004072866-A1
titleOfInvention Process for preparation of cyanophenylbenzoic acid derivatives
abstract A process for the production of a compound represented by the following Formula (IV) or a salt thereof, comprising the steps of condensing with dehydration a compound represent by the following Formula (I) and 4-(aminomethyl)piperidine to obtain a compound represented by the following Formula (II); protecting the secondary amine of the piperidine moiety to give a compound represented by the following Formula (III); and then reducing the imine moiety (in the Formulas, the wavy line may be, relative to the double bond, any of an E form, a Z form, or a mixture thereof, R represents a hydrogen atom, a C1-8 alkyl group etc., and R′ represents a C1-8 alkylcarbonyl group, an arylcarbonyl group etc.).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2003203935-A1
priorityDate 2001-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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