http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S59212468-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e7962109cd4763907b82b66760cd0ae8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-34
filingDate 1983-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6fb8e513c13b1ecaf63634376fbd4fc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_405acb04043af7113606b55d29cb3ac7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c0ccdcded6cc7480a0877f03cf3a1fd
publicationDate 1984-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S59212468-A
titleOfInvention 3-phenyl-4-cyanopyrrole derivative and production thereof
abstract NEW MATERIAL:A compound of formula I (R is lower alkyl; X is halogen; n is 0, 1 or 2). n EXAMPLE: 2-Ethoxycarbonyl-3-(2-chlorophenyl)-4-cyanopyrrole. n USE: An intermediate for medicines and agricultural chemicals, useful as an intermediate, etc. for producing pyrrole derivatives of formula II which are agricultural and horticultural germicides in high yield. n PREPARATION: A cinnamonitrile of formula III [Z is halogen, cyano or sulfonyl group of the formula SO 2 r (r is alkyl or aryl)] is reacted with an isocyanoacetic acid ester of formula IV in an organic solvent in the presence of a base or catalyst at room temperature W under cooling to give the aimed compound of formula I . n COPYRIGHT: (C)1984,JPO&Japio
priorityDate 1983-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 23.