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filingDate 2021-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-113501783-B
titleOfInvention A kind of erianin heterocyclic derivative and its preparation method and application
abstract The present invention relates to an Erianin heterocyclic derivative and its preparation method and application, wherein the structural formula of the Erianin heterocyclic derivative is: Wherein, X is O or NH; R is a furyl heterocyclic substituent, a thienyl heterocyclic substituent, a thiazolyl heterocyclic substituent, a pyrimidinyl heterocyclic substituent, a pyridazinyl heterocyclic substituent, a nicotinyl heterocyclic substituent, One of ring substituents and indolyl heterocyclic substituents; the preparation method includes: condensation reaction of erianin with a carboxylic acid compound containing substituent R; or 4-methoxy-3-nitrobenzene Formaldehyde and 3,4,5-trimethoxy-triphenylbenzyl bromide phosphine salt are used as raw materials, and after Wittig reaction and reduction reaction, condensation reaction is carried out with a carboxylic acid compound containing substituent R to obtain the above-mentioned Maolan Heterocyclic derivatives. Compared with the prior art, the present invention connects erianin with heterocyclic compounds such as nicotinic acid through ester bonds to form a twin drug, and provides a new way for improving the pharmacological activity of erianin.
priorityDate 2021-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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