http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105523988-B
Outgoing Links
Predicate | Object |
---|---|
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C319-20 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-58 |
filingDate | 2015-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2018-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2018-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-105523988-B |
titleOfInvention | A kind of preparation method of α-trifluoromethylthio-β-amino ketone, ester, nitrile or amide compound and α-trifluoromethylthio-β-amino acid |
abstract | The present invention relates to a preparation method of α-trifluoromethylthio-β-amino ketone, ester, nitrile or amide compound and α-trifluoromethylthio-β-amino acid. α-trifluoromethylthio-β-amino ketone, ester, nitrile or amide compounds are efficiently synthesized through difunctionalization reactions between phthalimide and ketones, esters, nitriles or amides, and in this compound On the basis of further conversion to α-trifluoromethylthio-β-amino acid. The present invention utilizes both parts of the N-SCF 3 reagent through 1,4 addition series reactions, and obtains a simple and efficient α-trifluoromethylthio-β-amino ketone, ester, nitrile or A method for synthesizing amide compounds and α-trifluoromethylthio-β-amino acids. |
priorityDate | 2015-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 117.