http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103724329-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8962e35aafcaf0b94f40e5dc67e61ab1
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-14
filingDate 2013-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67430a2c17049ada5e7d4da5569e5b71
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6926f6a2682a6db196493c106ebe924
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7d88666df730392c899a8a38c4c0a4c0
publicationDate 2015-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103724329-B
titleOfInvention Preparation method of 4-[5-(pyridyl-4-yl)-1H-[1,2,4]triazolyl-3-yl]pyridyl-2-formonitrile
abstract The invention provides a preparation method of 4-[5-(pyridyl-4-yl)-1H-[1,2,4]triazolyl-3-yl]pyridyl-2-formonitrile, which comprises the following steps: synthesizing a compound disclosed as Formula (V) from a compound disclosed as Formula (VI) as an initial raw material, synthesizing a compound disclosed as Formula (IV), synthesizing a compound disclosed as Formula (III), and finally synthesizing a compound disclosed as Formula (I) from the compound disclosed as Formula (III) and a compound disclosed as Formula (II). The method avoids using extremely toxic substances, has the advantages of high safety, environmental protection, short reaction time, mild reaction conditions, low product cost and high purity, and is simple to operate and suitable for industrial production. The reaction formula is disclosed in the specification.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016134854-A1
priorityDate 2013-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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