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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-14
filingDate 2006-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_551e15e2a48d0012c41049a6d6206839
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_96f9bd6339b14bd7983c327459143d68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dc54331e16a719493604f5086bad3a5a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c94b2e6304b3cb3233d4e66b4845c9b
publicationDate 2008-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2008007416-A
titleOfInvention N-substituted aniline derivatives, 1-substituted indole derivatives, 1- (1-pyridin-2-ylmethyl-piperidin-4-yl) -1H-indole and 3- (1-methyl-1H-indol-3-yl)- Process for producing 4- [1- [1- (pyridin-2-ylmethyl) piperidin-4-yl] -1H-indol-3-yl] -1H-pyrrole-2,5-dione
abstract 【Task】 Intermediate 1- (1-pyridin-2-ylmethyl-piperidin-4-yl) -1H-indole, which is important for producing enzastaurine useful as an anticancer agent, is inexpensively and efficiently produced in high yield To provide a manufacturing method capable of And a method for producing enzastaurine using the compound. [Solution] A method for producing a 1-substituted indole derivative in which a reductive amination reaction between an aniline derivative and a carbonyl compound is performed using hydrogen, followed by a cyclization reaction, and 1- (1 using the method for producing a 1-substituted indole derivative -Method for producing pyridin-2-ylmethyl-piperidin-4-yl) -1H-indole and enzastaurine.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009035537-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9951038-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2014102588-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9963458-B2
priorityDate 2006-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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