http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113968889-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_da488acbf12d11e33fe3429bf853bf9f
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J9-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J9-00
filingDate 2021-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7d801efebef9112f72bfa7493405e053
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_abef5856fdb4e6d38d8838ce3318dc3b
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publicationDate 2022-01-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-113968889-A
titleOfInvention Ring-opening composition and preparation method of brassinolide homologue intermediate
abstract The invention relates to a ring-opening composition and a preparation method of a brassinolide homologue intermediate. The ring-opening composition includes: pyridine-acid and p-toluenesulfonic acid; the intermediate is prepared by reacting an intermediate compound with the ring-opening composition, and the structural formula of the intermediate compound is: The structural formula of the intermediate is The present invention also provides a method for preparing a brassinolide homologue intermediate, which includes the following steps: mixing the intermediate compound, the above-mentioned ring-opening composition and a first solvent, and then performing reflux reaction at 140-180° C. to obtain the intermediate. The intermediate prepared by the invention has high yield and few isomer impurities, and the isomer impurity content can be as low as 0.43%.
priorityDate 2021-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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