http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-216013-A5

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-52
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filingDate 1983-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f3051643d3bc49f49a231f637ab71fbe
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f06358296948d334c20236ae729d7fa
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f13df88dc9b2293f23ac1ba5f0224643
publicationDate 1984-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-216013-A5
titleOfInvention PROCESS FOR THE PREPARATION OF NEW ETHENDIAMIN AND GUANIDINE DERIVATIVES
abstract The invention relates to a process for the preparation of novel compounds of general formula I, wherein, for example: R deep 1 is a C 1-C 6-lower alkyl-substituted C deep 3-C deep 10-cycloalkyl, an optionally C deep 1 -C deep 6-alkyl radicals substituted C deep 3-C deep 10-cycloalkyl-C deep 1-C deep 4-alkyl group, a C deep 6-C deep 8-bicycloalkyl group, a C deep 6-C deep 8-bicycloalkyl-C deep 1-C deep 4-alkyl group u. al .; R deep 2 hydrogen, a C 1-C deep deep 6-alkyl group, a phenyl-C 1-C deep deep 4-alkyl group or a C deep 1-C deep 6-alkyl group, by halogen atoms, nitro groups, hydroxy groups, C deep 2-C deeply substituted 6-alkanoyloxy groups, C 1-C deep deep 4-alkoxy groups, C 1-C deep deep 4-alkoxycarbonyl groups or carboxy groups; R 3 is hydrogen, the 2- (5- (dimethylaminomethyl) -2-furylmethylthio) -ethyl group, a C 1-C 1 deep C 18-alkyl group, and the like. al .; A is a nitrogen atom or a methine group, B is a cyano radical or a nitro group and X is an oxygen or sulfur atom and its salts. The compounds inhibit gastric juice secretion. In addition, they have an ulcer-inhibiting and gastricolytic effect.
priorityDate 1982-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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