http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114349704-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fd37b53f7a639daf413b490204ba4613
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-10
filingDate 2022-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_963fcc110f29749e0031a7fcc740b81e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dbc75c4e28bbbc80c0dff73f8e24818a
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publicationDate 2022-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-114349704-A
titleOfInvention Trifluoromethyl conjugated pyrazole spiro cyclopropane compound and synthesis method thereof
abstract The invention discloses trifluoromethyl conjugated pyrazole spiro propane compounds and a synthesis method thereof, belonging to the technical field of organic synthesis. Mixing substituted methylene cyclopropane 1, 1-substituted pyrazolidone compounds 2, inorganic base, copper salt or silver salt additive and trifluoroethanol 3, and heating to react to prepare trifluoromethyl conjugated pyrazole spiro cyclopropane compounds 4; the synthesis method is efficiently completed through one-pot series reaction among substituted methylene cyclopropane, 1-substituted pyrazolidone and trifluoroethanol, the whole process has high atom economy, mild reaction conditions and simple and efficient process; meanwhile, the method has the advantages of wide substrate range, good functional group tolerance and the like.
priorityDate 2022-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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