http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H11349577-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-14
filingDate 1999-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_43841207f083d4655bf4747bf4e947a1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd1b95da13563a22b322f06d2af70aaf
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publicationDate 1999-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H11349577-A
titleOfInvention Isoxazole derivative, 1,2,4-thiadiazol-3-ylacetic acid derivative, and method for producing the same
abstract (57) Abstract: A to provide a method for producing amino isoxazole derivatives useful as a raw material for the production of pharmaceutical and 1,2,4-thiadiazol-3-yl acetic acid derivatives (R 1 O) 2 The following method comprising a step of reacting a compound represented by C = CH-CN (R 1 represents an aryl group which may have a substituent) with hydroxylamine in the presence of a base (eg, an alkali metal alkoxide). Formula (I) And a method for producing a 1,2,4-thiadiazol-3-ylacetic acid derivative, comprising a step of reacting a thiocyanate and an acyl halide with the compound of the above formula (I). Embedded image
priorityDate 1998-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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