PROCESS FOR PREPARING N- (2- ((( 5-(DIMETHYLAMINO)-METHYL-2-FURANYL)METHYL)THIO) ETHYL-N-2-NITRO-1,1-ETHENEDIAMINE
Compd. of the formula (I) and their acid-addn. salts were prepd. Thus, a soln. of 198mg CuCl in 25ml acetonitrile was reacted with a soln. of 428mg 2-[[[5-(dimethylamino)methyl- 2 furanyl methyl thio ethaneamine, 296mg 1-methylthio-1-methylamino2- nitroethane, and 200mg TEA in 10ml acetonitrile. The...
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creator | JANKO ZMITEK HRIBAR-KIKELJ ALENKA LAH JOLANDA |
description | Compd. of the formula (I) and their acid-addn. salts were prepd. Thus, a soln. of 198mg CuCl in 25ml acetonitrile was reacted with a soln. of 428mg 2-[[[5-(dimethylamino)methyl- 2 furanyl methyl thio ethaneamine, 296mg 1-methylthio-1-methylamino2- nitroethane, and 200mg TEA in 10ml acetonitrile. The resulting ppt. was filtered and removed. The filtrate was mixed with 30ml chloroform and extd. with 20ml ammonia water 3 times. The organic phase was dried on Na2SO4, filtered, and vaporized to give (I)(yield, 94%). Compd. I inhibits the secretion of gastric acid stimulated by histamine-H2-acceptor. |
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Thus, a soln. of 198mg CuCl in 25ml acetonitrile was reacted with a soln. of 428mg 2-[[[5-(dimethylamino)methyl- 2 furanyl methyl thio ethaneamine, 296mg 1-methylthio-1-methylamino2- nitroethane, and 200mg TEA in 10ml acetonitrile. The resulting ppt. was filtered and removed. The filtrate was mixed with 30ml chloroform and extd. with 20ml ammonia water 3 times. The organic phase was dried on Na2SO4, filtered, and vaporized to give (I)(yield, 94%). Compd. I inhibits the secretion of gastric acid stimulated by histamine-H2-acceptor.</description><edition>4</edition><language>eng ; kor</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><creationdate>1987</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19870213&DB=EPODOC&CC=KR&NR=870000165B1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19870213&DB=EPODOC&CC=KR&NR=870000165B1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>JANKO ZMITEK</creatorcontrib><creatorcontrib>HRIBAR-KIKELJ ALENKA</creatorcontrib><creatorcontrib>LAH JOLANDA</creatorcontrib><title>PROCESS FOR PREPARING N- (2- ((( 5-(DIMETHYLAMINO)-METHYL-2-FURANYL)METHYL)THIO) ETHYL-N-2-NITRO-1,1-ETHENEDIAMINE</title><description>Compd. of the formula (I) and their acid-addn. salts were prepd. Thus, a soln. of 198mg CuCl in 25ml acetonitrile was reacted with a soln. of 428mg 2-[[[5-(dimethylamino)methyl- 2 furanyl methyl thio ethaneamine, 296mg 1-methylthio-1-methylamino2- nitroethane, and 200mg TEA in 10ml acetonitrile. The resulting ppt. was filtered and removed. The filtrate was mixed with 30ml chloroform and extd. with 20ml ammonia water 3 times. The organic phase was dried on Na2SO4, filtered, and vaporized to give (I)(yield, 94%). Compd. 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Thus, a soln. of 198mg CuCl in 25ml acetonitrile was reacted with a soln. of 428mg 2-[[[5-(dimethylamino)methyl- 2 furanyl methyl thio ethaneamine, 296mg 1-methylthio-1-methylamino2- nitroethane, and 200mg TEA in 10ml acetonitrile. The resulting ppt. was filtered and removed. The filtrate was mixed with 30ml chloroform and extd. with 20ml ammonia water 3 times. The organic phase was dried on Na2SO4, filtered, and vaporized to give (I)(yield, 94%). Compd. I inhibits the secretion of gastric acid stimulated by histamine-H2-acceptor.</abstract><edition>4</edition><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS |
title | PROCESS FOR PREPARING N- (2- ((( 5-(DIMETHYLAMINO)-METHYL-2-FURANYL)METHYL)THIO) ETHYL-N-2-NITRO-1,1-ETHENEDIAMINE |
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