http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010235527-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_268be9afa00cf55b5aa72b1612151ecb
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-85
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J21-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-85
filingDate 2009-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dc0e7d11d15ddfca526494e4e17f5475
publicationDate 2010-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2010235527-A
titleOfInvention Method for producing 2,6-diaminopyridine compound
abstract A method for producing a 2,6-diaminopyridine compound under mild reaction conditions is provided. In the presence of a metal catalyst, a compound such as dibutylamine is reacted with a compound such as 2,6-dichloro-3-cyano-4-methylpyridine, which is represented by the general formula (III). A method for producing 2,6-diaminopyridine compound. [In General Formula (III), R 11 , R 12 and R 13 each independently represent a hydrogen atom or a substituent. X represents a leaving group, and R 1 and R 2 each independently represent a hydrogen atom, an aliphatic group, an aromatic group, or a heterocyclic group. These groups may be further substituted. R 1 and R 2 may be bonded to each other to form a nitrogen-containing ring. ] [Selection figure] None
priorityDate 2009-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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