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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Hauptverfasser: CONOVER LLOYD HILLYARD, AUSTIN WILLIAM CHARLES, MACFARLAND JAMES WILLIAM
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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 &lt;FORM:1045838/C2/2&gt; where n is 2 or 3 and R2 represents an alkyl radical with 1 to 6 carbon atoms or a nitrile of formula &lt;FORM:1045838/C2/3&gt; 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 &lt;FORM:1045838/C3/1&gt; 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&amp;date=19661019&amp;DB=EPODOC&amp;CC=GB&amp;NR=1045838A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19661019&amp;DB=EPODOC&amp;CC=GB&amp;NR=1045838A$$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 &lt;FORM:1045838/C2/1&gt; 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 &lt;FORM:1045838/C2/2&gt; where n is 2 or 3 and R2 represents an alkyl radical with 1 to 6 carbon atoms or a nitrile of formula &lt;FORM:1045838/C2/3&gt; 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. 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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 &lt;FORM:1045838/C2/2&gt; where n is 2 or 3 and R2 represents an alkyl radical with 1 to 6 carbon atoms or a nitrile of formula &lt;FORM:1045838/C2/3&gt; 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 &lt;FORM:1045838/C3/1&gt; 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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