2-substituted thiophen derivatives
The invention comprises compounds of the formula where X represents -CH2-CH2-, -CH2-CH2-CH2- or -CH = CH-, Y represents -CH2-CH2- or -CH2-CH2-CH2-and R represents -H or -CH3, the non-toxic acid addition salts thereof, and methods for preparing these compounds. When X represents -CH2-CH2-or-CH2-CH2-...
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creator | CONOVER LLOYD HILLYARD AUSTIN WILLIAM CHARLES MACFARLAND JAMES WILLIAM |
description | The invention comprises compounds of the formula where X represents -CH2-CH2-, -CH2-CH2-CH2- or -CH = CH-, Y represents -CH2-CH2- or -CH2-CH2-CH2-and R represents -H or -CH3, the non-toxic acid addition salts thereof, and methods for preparing these compounds. When X represents -CH2-CH2-or-CH2-CH2-CH2-the thiophen derivatives are prepared by reacting an alkylene diamine, H2N-Y-NH.R, where Y and R are as defined above with either the hydrochloride or an imidate ester of formula where n is 2 or 3 and R2 represents an alkyl radical with 1 to 6 carbon atoms or a nitrile of formula where n is 2 or 3, in the presence of an organic sulphonic acid or gaseous hydrogen sulphide. When X represents -CH = CH-, an alkylene diamine is reacted with the hydrochloride of 3 - (11 - imino - 31 - (211 - thienyl)allyloxy) -propane sulphonic acid and, when required, isolating the desired free base from the resulting hydrochloride salt which latter compound is prepared by reacting 2-thienyl-acrylamide with 1,3-propane sultone. 3-(21-thienyl)propionitrile is prepared by hydrogenating 3-(21-thienyl)-acrylonitrile which is made by refluxing 2-thiophene - carboxaldehyde with cyanoacetic acid. Pharmaceutical compositions having anthelmintic activity contain as the active ingredient compounds of the first general formula where X, Y and R are as defined above and non-toxic acid addition salts thereof. The compositions may be administered as solutions, in admixture with feed or mineral supplements or in the form of tablets, boluses or capsules.ALSO:The invention comprises an adsorbate of compounds of general formula where X represents -CH2-CH2-, -CH2-CH2-CH2- or -CH = CH-, Y represents -CH2-CH2- or -CH2-CH2-CH2- and R represents -H or -CH3 and a cation-exchange resin such as the sodium form of a styrene/divinyl benzene copolymer having sulphonate cation-exchange groups. |
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When X represents -CH2-CH2-or-CH2-CH2-CH2-the thiophen derivatives are prepared by reacting an alkylene diamine, H2N-Y-NH.R, where Y and R are as defined above with either the hydrochloride or an imidate ester of formula <FORM:1045838/C2/2> where n is 2 or 3 and R2 represents an alkyl radical with 1 to 6 carbon atoms or a nitrile of formula <FORM:1045838/C2/3> where n is 2 or 3, in the presence of an organic sulphonic acid or gaseous hydrogen sulphide. When X represents -CH = CH-, an alkylene diamine is reacted with the hydrochloride of 3 - (11 - imino - 31 - (211 - thienyl)allyloxy) -propane sulphonic acid and, when required, isolating the desired free base from the resulting hydrochloride salt which latter compound is prepared by reacting 2-thienyl-acrylamide with 1,3-propane sultone. 3-(21-thienyl)propionitrile is prepared by hydrogenating 3-(21-thienyl)-acrylonitrile which is made by refluxing 2-thiophene - carboxaldehyde with cyanoacetic acid. Pharmaceutical compositions having anthelmintic activity contain as the active ingredient compounds of the first general formula where X, Y and R are as defined above and non-toxic acid addition salts thereof. The compositions may be administered as solutions, in admixture with feed or mineral supplements or in the form of tablets, boluses or capsules.ALSO:The invention comprises an adsorbate of compounds of general formula <FORM:1045838/C3/1> where X represents -CH2-CH2-, -CH2-CH2-CH2- or -CH = CH-, Y represents -CH2-CH2- or -CH2-CH2-CH2- and R represents -H or -CH3 and a cation-exchange resin such as the sodium form of a styrene/divinyl benzene copolymer having sulphonate cation-exchange groups.</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1966</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=19661019&DB=EPODOC&CC=GB&NR=1045838A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19661019&DB=EPODOC&CC=GB&NR=1045838A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>CONOVER LLOYD HILLYARD</creatorcontrib><creatorcontrib>AUSTIN WILLIAM CHARLES</creatorcontrib><creatorcontrib>MACFARLAND JAMES WILLIAM</creatorcontrib><title>2-substituted thiophen derivatives</title><description>The invention comprises compounds of the formula <FORM:1045838/C2/1> where X represents -CH2-CH2-, -CH2-CH2-CH2- or -CH = CH-, Y represents -CH2-CH2- or -CH2-CH2-CH2-and R represents -H or -CH3, the non-toxic acid addition salts thereof, and methods for preparing these compounds. When X represents -CH2-CH2-or-CH2-CH2-CH2-the thiophen derivatives are prepared by reacting an alkylene diamine, H2N-Y-NH.R, where Y and R are as defined above with either the hydrochloride or an imidate ester of formula <FORM:1045838/C2/2> where n is 2 or 3 and R2 represents an alkyl radical with 1 to 6 carbon atoms or a nitrile of formula <FORM:1045838/C2/3> where n is 2 or 3, in the presence of an organic sulphonic acid or gaseous hydrogen sulphide. When X represents -CH = CH-, an alkylene diamine is reacted with the hydrochloride of 3 - (11 - imino - 31 - (211 - thienyl)allyloxy) -propane sulphonic acid and, when required, isolating the desired free base from the resulting hydrochloride salt which latter compound is prepared by reacting 2-thienyl-acrylamide with 1,3-propane sultone. 3-(21-thienyl)propionitrile is prepared by hydrogenating 3-(21-thienyl)-acrylonitrile which is made by refluxing 2-thiophene - carboxaldehyde with cyanoacetic acid. Pharmaceutical compositions having anthelmintic activity contain as the active ingredient compounds of the first general formula where X, Y and R are as defined above and non-toxic acid addition salts thereof. The compositions may be administered as solutions, in admixture with feed or mineral supplements or in the form of tablets, boluses or capsules.ALSO:The invention comprises an adsorbate of compounds of general formula <FORM:1045838/C3/1> where X represents -CH2-CH2-, -CH2-CH2-CH2- or -CH = CH-, Y represents -CH2-CH2- or -CH2-CH2-CH2- and R represents -H or -CH3 and a cation-exchange resin such as the sodium form of a styrene/divinyl benzene copolymer having sulphonate cation-exchange groups.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1966</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFAy0i0uTSouySwpLUlNUSjJyMwvyEjNU0hJLcosSyzJLEst5mFgTUvMKU7lhdLcDPJuriHOHrqpBfnxqcUFicmpeakl8e5OhgYmphbGFo7GhFUAAENvJZM</recordid><startdate>19661019</startdate><enddate>19661019</enddate><creator>CONOVER LLOYD HILLYARD</creator><creator>AUSTIN WILLIAM CHARLES</creator><creator>MACFARLAND JAMES WILLIAM</creator><scope>EVB</scope></search><sort><creationdate>19661019</creationdate><title>2-substituted thiophen derivatives</title><author>CONOVER LLOYD HILLYARD ; AUSTIN WILLIAM CHARLES ; MACFARLAND JAMES WILLIAM</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_GB1045838A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1966</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>CONOVER LLOYD HILLYARD</creatorcontrib><creatorcontrib>AUSTIN WILLIAM CHARLES</creatorcontrib><creatorcontrib>MACFARLAND JAMES WILLIAM</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>CONOVER LLOYD HILLYARD</au><au>AUSTIN WILLIAM CHARLES</au><au>MACFARLAND JAMES WILLIAM</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>2-substituted thiophen derivatives</title><date>1966-10-19</date><risdate>1966</risdate><abstract>The invention comprises compounds of the formula <FORM:1045838/C2/1> where X represents -CH2-CH2-, -CH2-CH2-CH2- or -CH = CH-, Y represents -CH2-CH2- or -CH2-CH2-CH2-and R represents -H or -CH3, the non-toxic acid addition salts thereof, and methods for preparing these compounds. When X represents -CH2-CH2-or-CH2-CH2-CH2-the thiophen derivatives are prepared by reacting an alkylene diamine, H2N-Y-NH.R, where Y and R are as defined above with either the hydrochloride or an imidate ester of formula <FORM:1045838/C2/2> where n is 2 or 3 and R2 represents an alkyl radical with 1 to 6 carbon atoms or a nitrile of formula <FORM:1045838/C2/3> where n is 2 or 3, in the presence of an organic sulphonic acid or gaseous hydrogen sulphide. When X represents -CH = CH-, an alkylene diamine is reacted with the hydrochloride of 3 - (11 - imino - 31 - (211 - thienyl)allyloxy) -propane sulphonic acid and, when required, isolating the desired free base from the resulting hydrochloride salt which latter compound is prepared by reacting 2-thienyl-acrylamide with 1,3-propane sultone. 3-(21-thienyl)propionitrile is prepared by hydrogenating 3-(21-thienyl)-acrylonitrile which is made by refluxing 2-thiophene - carboxaldehyde with cyanoacetic acid. Pharmaceutical compositions having anthelmintic activity contain as the active ingredient compounds of the first general formula where X, Y and R are as defined above and non-toxic acid addition salts thereof. The compositions may be administered as solutions, in admixture with feed or mineral supplements or in the form of tablets, boluses or capsules.ALSO:The invention comprises an adsorbate of compounds of general formula <FORM:1045838/C3/1> where X represents -CH2-CH2-, -CH2-CH2-CH2- or -CH = CH-, Y represents -CH2-CH2- or -CH2-CH2-CH2- and R represents -H or -CH3 and a cation-exchange resin such as the sodium form of a styrene/divinyl benzene copolymer having sulphonate cation-exchange groups.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | 2-substituted thiophen derivatives |
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