1-Alkyl-4-alkoxy-2-quinolineones - as minor tranquillisers and their 3-carboxylic acid ester derivs. as inters
Cpds (I): (where R is 1-8C alkyl; R1 is H or 1-6C alkyl; R2 is 1-8C alkyl, and R3 is H, F, Cl, br or 1-4C alkoxy provided R2 is not Me when R is Me and R1 and R3 are both H) are prepd by reacting a cpd (I) (where R is H or alkali metal and R1, R2 and R3 are as defined, or R2 is H or alkali metal and...
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creator | G.E. HARDTMANN |
description | Cpds (I): (where R is 1-8C alkyl; R1 is H or 1-6C alkyl; R2 is 1-8C alkyl, and R3 is H, F, Cl, br or 1-4C alkoxy provided R2 is not Me when R is Me and R1 and R3 are both H) are prepd by reacting a cpd (I) (where R is H or alkali metal and R1, R2 and R3 are as defined, or R2 is H or alkali metal and R, R1 and R3 are as defined) with R6X (where R6 is 1-8C alkyl and X is Cl, Br I or OB; where B is MeSO2, PhSO2, or p-Me. C6H4SO2) or by reacting a cpd (IV) with (III) ot give (II) which is decarboxylated to give (I,R1=H) (where R4' is 1-8C alkyl; R9 is 1-4C alkyl; M is an alkali metal). Cpds (I) and (II) are used in the prepn of medicaments. |
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HARDTMANN</creatorcontrib><description>Cpds (I): (where R is 1-8C alkyl; R1 is H or 1-6C alkyl; R2 is 1-8C alkyl, and R3 is H, F, Cl, br or 1-4C alkoxy provided R2 is not Me when R is Me and R1 and R3 are both H) are prepd by reacting a cpd (I) (where R is H or alkali metal and R1, R2 and R3 are as defined, or R2 is H or alkali metal and R, R1 and R3 are as defined) with R6X (where R6 is 1-8C alkyl and X is Cl, Br I or OB; where B is MeSO2, PhSO2, or p-Me. C6H4SO2) or by reacting a cpd (IV) with (III) ot give (II) which is decarboxylated to give (I,R1=H) (where R4' is 1-8C alkyl; R9 is 1-4C alkyl; M is an alkali metal). Cpds (I) and (II) are used in the prepn of medicaments.</description><language>eng ; fre</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1974</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=19740430&DB=EPODOC&CC=BE&NR=806848A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19740430&DB=EPODOC&CC=BE&NR=806848A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>G.E. HARDTMANN</creatorcontrib><title>1-Alkyl-4-alkoxy-2-quinolineones - as minor tranquillisers and their 3-carboxylic acid ester derivs. as inters</title><description>Cpds (I): (where R is 1-8C alkyl; R1 is H or 1-6C alkyl; R2 is 1-8C alkyl, and R3 is H, F, Cl, br or 1-4C alkoxy provided R2 is not Me when R is Me and R1 and R3 are both H) are prepd by reacting a cpd (I) (where R is H or alkali metal and R1, R2 and R3 are as defined, or R2 is H or alkali metal and R, R1 and R3 are as defined) with R6X (where R6 is 1-8C alkyl and X is Cl, Br I or OB; where B is MeSO2, PhSO2, or p-Me. C6H4SO2) or by reacting a cpd (IV) with (III) ot give (II) which is decarboxylated to give (I,R1=H) (where R4' is 1-8C alkyl; R9 is 1-4C alkyl; M is an alkali metal). Cpds (I) and (II) are used in the prepn of medicaments.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1974</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFjEEKwkAMRbtxIeoVJBeIqC3SbZWKB3BfYhsxdMzUySj29o7g3tWH99__00w3WLl-dFggud6_R9zi4ynqnSh7ZQMEMrgnEiAG0lQ6J8bBgLSDeGMJkGNL4ZLWTlqgVjpgixyg4yAvW30fRBOweTa5kjNe_HKWLY_1-XBCHnzDNlDLyrHZ1-V6VxZllf8VPmq2QBQ</recordid><startdate>19740430</startdate><enddate>19740430</enddate><creator>G.E. HARDTMANN</creator><scope>EVB</scope></search><sort><creationdate>19740430</creationdate><title>1-Alkyl-4-alkoxy-2-quinolineones - as minor tranquillisers and their 3-carboxylic acid ester derivs. as inters</title><author>G.E. HARDTMANN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_BE806848A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre</language><creationdate>1974</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>G.E. HARDTMANN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>G.E. HARDTMANN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>1-Alkyl-4-alkoxy-2-quinolineones - as minor tranquillisers and their 3-carboxylic acid ester derivs. as inters</title><date>1974-04-30</date><risdate>1974</risdate><abstract>Cpds (I): (where R is 1-8C alkyl; R1 is H or 1-6C alkyl; R2 is 1-8C alkyl, and R3 is H, F, Cl, br or 1-4C alkoxy provided R2 is not Me when R is Me and R1 and R3 are both H) are prepd by reacting a cpd (I) (where R is H or alkali metal and R1, R2 and R3 are as defined, or R2 is H or alkali metal and R, R1 and R3 are as defined) with R6X (where R6 is 1-8C alkyl and X is Cl, Br I or OB; where B is MeSO2, PhSO2, or p-Me. C6H4SO2) or by reacting a cpd (IV) with (III) ot give (II) which is decarboxylated to give (I,R1=H) (where R4' is 1-8C alkyl; R9 is 1-4C alkyl; M is an alkali metal). Cpds (I) and (II) are used in the prepn of medicaments.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | 1-Alkyl-4-alkoxy-2-quinolineones - as minor tranquillisers and their 3-carboxylic acid ester derivs. as inters |
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