Process for the preparation of new methylamine derivatives
The methylamine derivatives of general formula: and their non-toxic addition salts, in which R represents n-propyl, isopropyl, isobutyl or allyl, R1 represents hydrogen, methyl or propargyl and R2 represents methyl or propargyl, are obtained by heating an amine, which is unsubstituted or R1-substitu...
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creator | MADELEINE BROLL CHARLES PIGEROL JEAN-CLAUDE VERNIERES PIERRE EYMARD |
description | The methylamine derivatives of general formula: and their non-toxic addition salts, in which R represents n-propyl, isopropyl, isobutyl or allyl, R1 represents hydrogen, methyl or propargyl and R2 represents methyl or propargyl, are obtained by heating an amine, which is unsubstituted or R1-substituted on the nitrogen, with a methyl or propargyl halide in the presence of an alkaline agent to produce a basic methylamine derivative which is reacted with an acid to produce a non-toxic addition salt. The methylamine derivatives in question are useful in human or veterinary medicine as antiparkinsonian agents or correctors of extrapyramidal disorders due to neuroleptics. They are less inhibiting of monoamine oxidase than the corresponding derivatives which are unsubstituted on the nitrogen and have, for this reason, fewer side effects. |
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The methylamine derivatives in question are useful in human or veterinary medicine as antiparkinsonian agents or correctors of extrapyramidal disorders due to neuroleptics. They are less inhibiting of monoamine oxidase than the corresponding derivatives which are unsubstituted on the nitrogen and have, for this reason, fewer side effects.</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>1981</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=19810831&DB=EPODOC&CC=CH&NR=624922A5$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25543,76293</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19810831&DB=EPODOC&CC=CH&NR=624922A5$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>MADELEINE BROLL</creatorcontrib><creatorcontrib>CHARLES PIGEROL</creatorcontrib><creatorcontrib>JEAN-CLAUDE VERNIERES</creatorcontrib><creatorcontrib>PIERRE EYMARD</creatorcontrib><title>Process for the preparation of new methylamine derivatives</title><description>The methylamine derivatives of general formula: and their non-toxic addition salts, in which R represents n-propyl, isopropyl, isobutyl or allyl, R1 represents hydrogen, methyl or propargyl and R2 represents methyl or propargyl, are obtained by heating an amine, which is unsubstituted or R1-substituted on the nitrogen, with a methyl or propargyl halide in the presence of an alkaline agent to produce a basic methylamine derivative which is reacted with an acid to produce a non-toxic addition salt. The methylamine derivatives in question are useful in human or veterinary medicine as antiparkinsonian agents or correctors of extrapyramidal disorders due to neuroleptics. They are less inhibiting of monoamine oxidase than the corresponding derivatives which are unsubstituted on the nitrogen and have, for this reason, fewer side effects.</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>1981</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZLAKKMpPTi0uVkjLL1IoyUhVKChKLUgsSizJzM9TyE9TyEstV8hNLcmozEnMzcxLVUhJLcosA8qWpRbzMLCmJeYUp_JCaW4GeTfXEGcP3dSC_PjU4oLE5NS81JJ4Zw8zIxNLIyNHU2PCKgDlQC6b</recordid><startdate>19810831</startdate><enddate>19810831</enddate><creator>MADELEINE BROLL</creator><creator>CHARLES PIGEROL</creator><creator>JEAN-CLAUDE VERNIERES</creator><creator>PIERRE EYMARD</creator><scope>EVB</scope></search><sort><creationdate>19810831</creationdate><title>Process for the preparation of new methylamine derivatives</title><author>MADELEINE BROLL ; CHARLES PIGEROL ; JEAN-CLAUDE VERNIERES ; PIERRE EYMARD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CH624922A53</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1981</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>MADELEINE BROLL</creatorcontrib><creatorcontrib>CHARLES PIGEROL</creatorcontrib><creatorcontrib>JEAN-CLAUDE VERNIERES</creatorcontrib><creatorcontrib>PIERRE EYMARD</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>MADELEINE BROLL</au><au>CHARLES PIGEROL</au><au>JEAN-CLAUDE VERNIERES</au><au>PIERRE EYMARD</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Process for the preparation of new methylamine derivatives</title><date>1981-08-31</date><risdate>1981</risdate><abstract>The methylamine derivatives of general formula: and their non-toxic addition salts, in which R represents n-propyl, isopropyl, isobutyl or allyl, R1 represents hydrogen, methyl or propargyl and R2 represents methyl or propargyl, are obtained by heating an amine, which is unsubstituted or R1-substituted on the nitrogen, with a methyl or propargyl halide in the presence of an alkaline agent to produce a basic methylamine derivative which is reacted with an acid to produce a non-toxic addition salt. The methylamine derivatives in question are useful in human or veterinary medicine as antiparkinsonian agents or correctors of extrapyramidal disorders due to neuroleptics. They are less inhibiting of monoamine oxidase than the corresponding derivatives which are unsubstituted on the nitrogen and have, for this reason, fewer side effects.</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 | Process for the preparation of new methylamine derivatives |
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