Predicate |
Object |
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 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114790173-B http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114790173-A 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 |