http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H09309873-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_eb6feebb52dc907a08ae0244105bc319
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C277-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C279-18
filingDate 1996-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_308e8e36025dc912c555f1645820b78c
publicationDate 1997-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H09309873-A
titleOfInvention A new method for producing camostat mesylate.
abstract (57) Abstract: [PROBLEMS] To provide a method for producing camostat mesilate, which can be industrially produced in high yield and easily. SOLUTION: 4-Guanidinobenzoic acid or its reactive derivative and 4-hydroxyphenylacetic acid N, N-dimethylcarbamoylmethyl ester are subjected to an esterification reaction in the presence of dicyclohexylcarbodiimide, and the esterification reaction step or ester At the stage of completion of the chemical reaction, p-toluenesulfonic acid in a stoichiometric amount or more is added to the reaction system for treatment, and the resulting camostat is isolated as p-toluenesulfonic acid salt. A method for producing camostat mesylate, which is treated with an aqueous solution of sodium hydrogencarbonate, converted to a carbonate of camostat, purified, and then treated with methanesulfonic acid.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006108643-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1736153-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010229141-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2023148783-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110330447-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002114755-A
priorityDate 1996-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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