ALPHA-CYCLIC AMINOPHENYLACETIC ESTERS, THEIR ACID ADDITION SALTS AND QUATERNARY AMMONIUM SALTS
NEW MATERIAL:A compound shown by the formula I (R1 is H, halogen, OH, lower alkyl, CF3, or lower alkoxy; R2 is lower alkyl; Am is 5-9-membered cyclic amino group which may be replaced with lower alkyl; m and n are 1, 2, or 3, and m+n is 3, 4, or 5; with the proviso that a case where Am is piperidino...
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creator | KADOKAWA TOSHIAKI NISHIMURA ATSUKI KAWASHIMA KATSUYOSHI NARUTO SHIYUNSUKE MIZUTA YASUYUKI |
description | NEW MATERIAL:A compound shown by the formula I (R1 is H, halogen, OH, lower alkyl, CF3, or lower alkoxy; R2 is lower alkyl; Am is 5-9-membered cyclic amino group which may be replaced with lower alkyl; m and n are 1, 2, or 3, and m+n is 3, 4, or 5; with the proviso that a case where Am is piperidino, m is 3 and n is 1 is omitted), its pharmaceutically acceptable acid addition salts and quaternary ammonium salts. EXAMPLE:1-Methyl-4-piperidyl alpha-hexamethyleneimidophenylacetate dihydrochloride. USE:Having antispasmodic action with high acetylcholine resistance of a drug such as an antispasmodic, etc., furthermore having low side effect such as mydriasis, inhibition of spittle secretion, pulsus frequens, etc. PROCESS:A compound shown by the formula II (Hal is halogen such as Cl, Br, or I) or its acid addition salt is reacted with a compound shown by the formula H-Am, to give a compound shown by the formula I . |
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EXAMPLE:1-Methyl-4-piperidyl alpha-hexamethyleneimidophenylacetate dihydrochloride. USE:Having antispasmodic action with high acetylcholine resistance of a drug such as an antispasmodic, etc., furthermore having low side effect such as mydriasis, inhibition of spittle secretion, pulsus frequens, etc. PROCESS:A compound shown by the formula II (Hal is halogen such as Cl, Br, or I) or its acid addition salt is reacted with a compound shown by the formula H-Am, to give a compound shown by the formula I .</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><creationdate>1983</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=19831203&DB=EPODOC&CC=JP&NR=S58208270A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19831203&DB=EPODOC&CC=JP&NR=S58208270A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>KADOKAWA TOSHIAKI</creatorcontrib><creatorcontrib>NISHIMURA ATSUKI</creatorcontrib><creatorcontrib>KAWASHIMA KATSUYOSHI</creatorcontrib><creatorcontrib>NARUTO SHIYUNSUKE</creatorcontrib><creatorcontrib>MIZUTA YASUYUKI</creatorcontrib><title>ALPHA-CYCLIC AMINOPHENYLACETIC ESTERS, THEIR ACID ADDITION SALTS AND QUATERNARY AMMONIUM SALTS</title><description>NEW MATERIAL:A compound shown by the formula I (R1 is H, halogen, OH, lower alkyl, CF3, or lower alkoxy; R2 is lower alkyl; Am is 5-9-membered cyclic amino group which may be replaced with lower alkyl; m and n are 1, 2, or 3, and m+n is 3, 4, or 5; with the proviso that a case where Am is piperidino, m is 3 and n is 1 is omitted), its pharmaceutically acceptable acid addition salts and quaternary ammonium salts. EXAMPLE:1-Methyl-4-piperidyl alpha-hexamethyleneimidophenylacetate dihydrochloride. USE:Having antispasmodic action with high acetylcholine resistance of a drug such as an antispasmodic, etc., furthermore having low side effect such as mydriasis, inhibition of spittle secretion, pulsus frequens, etc. PROCESS:A compound shown by the formula II (Hal is halogen such as Cl, Br, or I) or its acid addition salt is reacted with a compound shown by the formula H-Am, to give a compound shown by the formula I .</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1983</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNjL0KwjAURrs4iPoO191CqYhdL0kkV_Jnkg5ZLEXiJFqo748BfQCnD845fMvqispJrFliihigJmOdFCYpZCIWIkIUPuwgSkEekBEH5JwiWQMBVQyAhsOlx5IZ9KlcaGuo11-7rhb38THnzW9X1fYkIpN1nl5Dnqfxlp_5PZxdOHRt07XHBvf_NB8iKjM_</recordid><startdate>19831203</startdate><enddate>19831203</enddate><creator>KADOKAWA TOSHIAKI</creator><creator>NISHIMURA ATSUKI</creator><creator>KAWASHIMA KATSUYOSHI</creator><creator>NARUTO SHIYUNSUKE</creator><creator>MIZUTA YASUYUKI</creator><scope>EVB</scope></search><sort><creationdate>19831203</creationdate><title>ALPHA-CYCLIC AMINOPHENYLACETIC ESTERS, THEIR ACID ADDITION SALTS AND QUATERNARY AMMONIUM SALTS</title><author>KADOKAWA TOSHIAKI ; NISHIMURA ATSUKI ; KAWASHIMA KATSUYOSHI ; NARUTO SHIYUNSUKE ; MIZUTA YASUYUKI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JPS58208270A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1983</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><toplevel>online_resources</toplevel><creatorcontrib>KADOKAWA TOSHIAKI</creatorcontrib><creatorcontrib>NISHIMURA ATSUKI</creatorcontrib><creatorcontrib>KAWASHIMA KATSUYOSHI</creatorcontrib><creatorcontrib>NARUTO SHIYUNSUKE</creatorcontrib><creatorcontrib>MIZUTA YASUYUKI</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>KADOKAWA TOSHIAKI</au><au>NISHIMURA ATSUKI</au><au>KAWASHIMA KATSUYOSHI</au><au>NARUTO SHIYUNSUKE</au><au>MIZUTA YASUYUKI</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>ALPHA-CYCLIC AMINOPHENYLACETIC ESTERS, THEIR ACID ADDITION SALTS AND QUATERNARY AMMONIUM SALTS</title><date>1983-12-03</date><risdate>1983</risdate><abstract>NEW MATERIAL:A compound shown by the formula I (R1 is H, halogen, OH, lower alkyl, CF3, or lower alkoxy; R2 is lower alkyl; Am is 5-9-membered cyclic amino group which may be replaced with lower alkyl; m and n are 1, 2, or 3, and m+n is 3, 4, or 5; with the proviso that a case where Am is piperidino, m is 3 and n is 1 is omitted), its pharmaceutically acceptable acid addition salts and quaternary ammonium salts. EXAMPLE:1-Methyl-4-piperidyl alpha-hexamethyleneimidophenylacetate dihydrochloride. USE:Having antispasmodic action with high acetylcholine resistance of a drug such as an antispasmodic, etc., furthermore having low side effect such as mydriasis, inhibition of spittle secretion, pulsus frequens, etc. PROCESS:A compound shown by the formula II (Hal is halogen such as Cl, Br, or I) or its acid addition salt is reacted with a compound shown by the formula H-Am, to give a compound shown by the formula I .</abstract><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 |
title | ALPHA-CYCLIC AMINOPHENYLACETIC ESTERS, THEIR ACID ADDITION SALTS AND QUATERNARY AMMONIUM SALTS |
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