http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2565790-C1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-36
filingDate 2014-11-13^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-10-20^^<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_6c809bcba7f2b657e583bdba90605314
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publicationDate 2015-10-20^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2565790-C1
titleOfInvention Method of producing n-cyclopentyl-substituted 1,5,3-dithiazepanes
abstract FIELD: chemistry. n SUBSTANCE: invention relates to a method of producing N-cyclopentyl-substituted 1,5,3-dithiazepanes of general formula: n where characterised by that an N-cyclopentyl-substituted amine (cyclopentyl-amine, pyrrolidine-3-amine, 2-amino-norbornane) reacts with 1-oxa-3,6-dithiacycloheptane in the presence of a SmCl 3 ·6H 2 O catalyst with molar ratio N-cyclopentyl-substituted amine:1-oxa-3,6-dithiacycloheptane:SmCl 3 ·6H 2 O = 1:1:(0.03-0.07) at room temperature (~20°C) in an ethanol-chloroform solvent medium (1:1, volume ratio) for 2.5-3.5 hours. n EFFECT: compounds can be used as antimicrobial, antifungal and anti-inflammatory agents, as well selective complexing agents. n 1 tbl, 1 ex
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priorityDate 2014-11-13^^<http://www.w3.org/2001/XMLSchema#date>
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