http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108623455-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-738
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-313
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C59-84
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-738
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-313
filingDate 2017-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108623455-B
titleOfInvention Intermediate of anti-heart failure medicine
abstract The invention discloses an intermediate of an anti-heart failure drug, which is shown as a compound in a formula IV. The intermediate takes malonate (formula VI) as raw material and sulfonyl protected ( R ) -lactate (formula VII) undergoes a nucleophilic substitution reaction to give a compound of formula V, which is then condensed with 4-biphenylacetyl chloride to give a compound of formula IV. The invention also discloses application of the compound shown in the formula IV, which is a key intermediate for preparing the compound shown in the formula I. Specifically, the compound of formula IV is subjected to decarboxylation to obtain a compound of formula III, and the compound of formula III is subjected to hydrolysis, salifying with organic amine and purification to obtain the compound of formula I.
priorityDate 2017-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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