http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103664913-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a544c49cadf466ab6f2337003140df2e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_385f84ec011382ecd8628ec07c5fea83
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-14
filingDate 2012-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_78b674c3c09cd023a237380a762d469d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf1db2d36362490edc6f8bd7f2241495
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a700eaeac29b0d3712e8f774430a41d5
publicationDate 2014-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103664913-A
titleOfInvention Preparation method of olmesartan medoxomil
abstract The invention discloses a preparation method of olmesartan medoxomil. The method comprises a step of de-protecting a compound shown by the formula V in an organic solvent containing p-toluenesulfonic acid to obtain olmesartan medoxomil. The structure of the compound shown by the formula V is shown in the specification. The method disclosed by the invention has the advantages of cheap and easily-available raw materials, mild reaction conditions, high reaction selectivity, high yield and few byproducts and is suitable for industrial production.
priorityDate 2012-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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