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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
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filingDate 1995-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8e13eebe6446c5223cf08bc5bc573141
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5cc1e0f268e4a82e487084537e09fb6d
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publicationDate 1996-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H08268988-A
titleOfInvention Aminobenzamide compound and its production method
abstract (57) [Summary] [Objective] 3- [2- (3,4-dimethoxyphenyl) ethylcarbamoylmethyl] amino-N-methylbenzamide [final compound], which is useful as an anti-ulcer drug and an effect of improving indefinite complaints Regarding the production method, it is an object of the present invention to provide an industrial production method and a synthetic intermediate thereof, which uses a solvent non-toxic to the human body and produces a small amount of by-products. [Structure] (1) As a synthetic intermediate (iodoacetyl) Provide -3,4-dimethoxyphenethylamine. (2) N- (chloroacetyl) -3,4-dimethoxy is acetylated to 3,4-dimethoxyphenethylamine in the presence of a ketone or alcohol, which is sparingly soluble in water and liquid at room temperature. Phenethylamine is produced, and then the product is reacted with hydroiodide under the same solvent to produce N- (iodoacetyl) -3,4-dimethoxyphenethylamine. A method for producing the above-mentioned final compound which is crystallized via a monohydrate by reacting with amino-N-methylbenzamide.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008247753-A
priorityDate 1995-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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