http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2013006778-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fec576c38e34882531ca37d6b922bf42
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-14
filingDate 2011-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e21b059b0d8af769c0d5f2ec7507ba7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_60ce9ae65e695540cb20cac64647e136
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_321045eef5dfdb9f9cca624dd695a4c9
publicationDate 2013-01-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2013006778-A
titleOfInvention Method for producing pyrazole compound
abstract The present invention provides a 1,3-disubstituted pyrazole-4-carboxylic acid ester having high efficiency and a small amount of isomer formation. SOLUTION: A carboxylic acid halide and a dialkylaminoacrylic acid ester are reacted in a solvent in the presence of an organic base, and the organic base / hydrogen fluoride salt is separated and removed by filtration. The manufacturing method which produces | generates a pyrazole compound by. (In the formula, each R independently represents an alkyl group or an aryl group, and X represents a halogen atom.) [Selection figure] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10239841-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016152886-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8871947-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9139507-B2
priorityDate 2011-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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