http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103351331-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_db6466407cfaa9e805ff333d96919ba6
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-40
filingDate 2013-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d2ea298a26732a28cb0336569f381616
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e50554e64ebfe21252d3afb0b51bd904
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_562479a331b025f355574db4e205eb8b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_406303e188f678bc1a73af65446e6065
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0aee596d98590b73a3ac327b89fdafc7
publicationDate 2015-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103351331-B
titleOfInvention Marine natural product Echinoclathrine A preparation method
abstract The invention relates to a marine natural product Echinoclathrine A preparation method and belongs to the technical field of pharmaceutical chemicals. In order to solve the problems that the existing technology is simple and low in yield, the invention provides the marine natural product Echinoclathrine A preparation method. The preparation method comprises the following steps: with an acid application agent, 3-cl-2-aminophenol and n-butyryl chloride butanoyl chloride perform a substitution reaction in halogenated hydrocarbon to acquire an intermediate product; under the function of an alkaline reagent, with a palladium catalyst and a phosphorus compound, the intermediate product and 2-methyl pyridine boric acid have a reaction to acquire the final product Echinoclathrine A. The preparation method has the advantages of simple technology, and high product purity and yield.
priorityDate 2013-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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