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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_511e4fe177b73690190f25a66a1dfd62
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P13-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-08
filingDate 1991-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e097149307bbd7938fab32d1f2a4a75e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f75b964bcc95fc06cf704b6fb4beff49
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bcf91d3e42b91a812da5d2f4c1b2b17b
publicationDate 1997-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2076098-C1
titleOfInvention 3'-(2-amino-1-hydroxyethyl)-4'-fluoromethanesulfoneanilide and agent for enuresis treatment
abstract FIELD: organic chemistry. SUBSTANCE: product: 3'-(2-amino-1-hydroxyethyl)-4'-fluoromethanesulfoneamide or its optically active isomers, pharmacological salts, m. p. is 176-179 C, empirical formula is C 9 H 13 FN 2 O 3 . Reagent 1: 3'-(2-aminoacetyl)-4'-fluoromethanesulfone anilide. Reagent 2: sodium borohydride. Reaction condition: in methanol medium, at heating. Synthesized compound is used in medicine. EFFECT: improved method of synthesis. 2 cl, 5 tbl
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2446167-C2
priorityDate 1990-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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