http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2565790-C1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3ff5107449ebdaf88df149b6b4c15ec1 |
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 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d5eec11b6718a8c29f7f03dab39ce815 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_01b939c2088e926624db0cb1fb170b48 |
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 |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2664655-C2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2664654-C2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2601313-C1 |
priorityDate | 2014-11-13^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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