http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2529516-C2

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-36
filingDate 2012-10-19^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-09-27^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f72ba1d64d43b296651f0a9a452216a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_01b939c2088e926624db0cb1fb170b48
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publicationDate 2014-09-27^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2529516-C2
titleOfInvention Method of obtaining 4-(1,5,3-dithiazepinan-3-yl)-benzoic and 5-(1,5,3-dithiazepinan-3-yl)-2-hydroxybenzoic acids
abstract FIELD: chemistry. n SUBSTANCE: invention relates to field of organic chemistry, in particular to method of obtaining 4-(1,5,3-dithiazepinan-3-yl)-benzoic and 5-(1,5,3-dithiazepinan-3-yl)-2-hydroxybenzoic acids of general formula (1) consisting in the following: aminobenzoic acid (4-aminobenzoic or 2-hydroxy-5-aminobenzoic) is subjected to interaction with 1-oxa-3,6-dithiacycloheptane in presence of catalyst Sm(NO 3 ) 3   · 6H 2 O with molar ratio aminobenzoic acid: 1-oxa-3,6-dithiacycloheptane:Sm(NO 3 ) 3   · 6H 2 O=10:10:(0.3-0.7) at room temperature (~20°C) in medium of solvents ethanol-chloroform (1:1, volume ratio) and argon atmosphere for 2.5-3.5 h. n EFFECT: elaborated is method of obtaining 4-(1,5,3-dithiazepinan-3-yl)-benzoic and 5-(1,5,3-dithiazepinan-3-yl)-2-hydroxybenzoic acids. n 1 tbl, 1 ex
priorityDate 2012-10-19^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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