http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102532015-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_56d9856858f491640008656f9086efaa
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-227
filingDate 2012-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_33b9dfa071b99b79c1d345be428700d3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_609cbcf73b8dffbd300e6e38e59ba3ac
publicationDate 2013-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102532015-B
titleOfInvention Solid-phase synthesis method of coumarin and analogue thereof
abstract The invention relates to a solid-phase synthesis method of coumarin and an analogue (I) thereof and belongs to the field of organic chemistry. The method comprises the following steps: 1) taking 1% of cross-linked polystyrene resin as a carrier to prepare a polystyrene-supported seleno-succimide reagent (III); 2) using the III to induce phenyl acrylate (V) to perform intramolecular cyclization under the catalysis of trimethylsilyl trifluoromethanesulfonate so as to form 3-polystyrene-supported seleno-3,4-dihydro-benzopyran-2-ketone (VI); and 3) performing oxidation elimination on the VI via an oxidant so as to directly get the coumarin (I) without further separation. When the phenyl acrylate (V) is replaced by N-phenyl acrylamide, the analogue of the coumarin, namely a 2-quinolone compound, can be prepared through the same steps. The solid-phase synthesis method disclosed by the invention has the advantages of easily available raw materials, good product yield, high purity, simplicityand convenience in operation, simple post-treatment and great industrial application prospects.
priorityDate 2012-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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