http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111333552-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C315-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C315-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C317-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C317-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C315-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C315-00
filingDate 2020-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-111333552-B
titleOfInvention Synthesis method of beta-benzo amino acid compound
abstract The invention relates to a preparation method of a beta-benzo amino acid compound, which comprises the following steps: (1) obtaining a racemate compound shown as a formula (I); (2) reacting a racemate compound shown as a formula (I) with L-aspartic acid to obtain a compound shown as a formula (I-1); and/or reacting the racemate compound shown in the formula (I) with D-aspartic acid to obtain a compound shown in the formula (I-2); (3) introducing a protecting group on an amine group in the compound shown in the formula (I-1) and/or the compound shown in the formula (I-2), and then carrying out a transesterification reaction. The synthesis method can obtain the beta-benzo amino acid compounds with different configurations without chiral chromatographic resolution, has low cost, simple operation and convenient industrial application, and the product has high chiral purity and high yield.
priorityDate 2020-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 50.