Procédé de préparation de dérivés de polyols utiles en thérapeutique
Mono-, di-, tri- and tetra-esters derived from an acid of the general formula: R-OH in which R represents an acyl radical of the general formula: in which n represents 0 or 1, m represents 0, 1, 2, 3 or 4, R1 and R2 each represent a straight- or branched-chain alkyl radical having from 1 to 5 carbon...
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creator | CHARLES PIGEROL BERNARD FERRANDES MICHEL CHIGNAC CLAUDE GRAIN FERNAND JAMMOT PIERRE EYMARD |
description | Mono-, di-, tri- and tetra-esters derived from an acid of the general formula: R-OH in which R represents an acyl radical of the general formula: in which n represents 0 or 1, m represents 0, 1, 2, 3 or 4, R1 and R2 each represent a straight- or branched-chain alkyl radical having from 1 to 5 carbon atoms, R3 represents hydrogen or a straight- or branched-chain alkyl radical having from 1 to 5 carbon atoms, the sum of the carbon atoms in R1 and R2 being from 4 to 10 when R3 represents hydrogen and the sum of the carbon atoms in R1, R2 and R3 being from 6 to 15 when R3 is different from hydrogen, or R1 and R2 when they are taken together represent a tetramethylene, pentamethylene or hexamethylene radical and R3 represents a straight-chain alkyl radical and an alcohol selected from the group consisting of glycerol, 2,3-epoxy-propanol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,2,3-butanetriol, 1,2,4-butanetriol, 1,2,3,4-butanetetrol, 2-buten-1,4-diol, 2-butyn-1,4-diol, diethyleneglycol, a cyclohexanediol preferably 1,2-cyclohexanediol, thiodiglycol, diethanolamine, N-R-substituted-diethanolamine, trimethylolpropane, pentaerythritol and an alcohol of the general formula: II in which p represents 0 or 1, R4 represents methyl, R5 represents methyl, ethyl, 2-methyl-butyl or R4 and R5, when they are taken together represent a pentamethylene radical, with the exception of glyceryl tri-(di-n-propylacetate). These esters are useful in the treatment of central nervous system disorders and including, in particular, convulsive states and seizures, and disorders relating to the field of neuropsychiatry. |
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These esters are useful in the treatment of central nervous system disorders and including, in particular, convulsive states and seizures, and disorders relating to the field of neuropsychiatry.</description><edition>3</edition><language>fre</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</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=OA&NR=6568A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19810831&DB=EPODOC&CC=OA&NR=6568A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>CHARLES PIGEROL</creatorcontrib><creatorcontrib>BERNARD FERRANDES</creatorcontrib><creatorcontrib>MICHEL CHIGNAC</creatorcontrib><creatorcontrib>CLAUDE GRAIN</creatorcontrib><creatorcontrib>FERNAND JAMMOT</creatorcontrib><creatorcontrib>PIERRE EYMARD</creatorcontrib><title>Procédé de préparation de dérivés de polyols utiles en thérapeutique</title><description>Mono-, di-, tri- and tetra-esters derived from an acid of the general formula: R-OH in which R represents an acyl radical of the general formula: in which n represents 0 or 1, m represents 0, 1, 2, 3 or 4, R1 and R2 each represent a straight- or branched-chain alkyl radical having from 1 to 5 carbon atoms, R3 represents hydrogen or a straight- or branched-chain alkyl radical having from 1 to 5 carbon atoms, the sum of the carbon atoms in R1 and R2 being from 4 to 10 when R3 represents hydrogen and the sum of the carbon atoms in R1, R2 and R3 being from 6 to 15 when R3 is different from hydrogen, or R1 and R2 when they are taken together represent a tetramethylene, pentamethylene or hexamethylene radical and R3 represents a straight-chain alkyl radical and an alcohol selected from the group consisting of glycerol, 2,3-epoxy-propanol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,2,3-butanetriol, 1,2,4-butanetriol, 1,2,3,4-butanetetrol, 2-buten-1,4-diol, 2-butyn-1,4-diol, diethyleneglycol, a cyclohexanediol preferably 1,2-cyclohexanediol, thiodiglycol, diethanolamine, N-R-substituted-diethanolamine, trimethylolpropane, pentaerythritol and an alcohol of the general formula: II in which p represents 0 or 1, R4 represents methyl, R5 represents methyl, ethyl, 2-methyl-butyl or R4 and R5, when they are taken together represent a pentamethylene radical, with the exception of glyceryl tri-(di-n-propylacetate). These esters are useful in the treatment of central nervous system disorders and including, in particular, convulsive states and seizures, and disorders relating to the field of neuropsychiatry.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><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><subject>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1981</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZPAKKMpPPrwy5fBKhZRUhYKiwysLEosSSzLz80B8oHBRZtnhlcVgyfycyvycYoXSksyc1GKF1DyFkgygfGJBKlCksDSVh4E1LTGnOJUXSnMzyLi5hjh76KYW5MenFhckJqfmpZbE-zuamZpZOBoTkAYAHZc3Ng</recordid><startdate>19810831</startdate><enddate>19810831</enddate><creator>CHARLES PIGEROL</creator><creator>BERNARD FERRANDES</creator><creator>MICHEL CHIGNAC</creator><creator>CLAUDE GRAIN</creator><creator>FERNAND JAMMOT</creator><creator>PIERRE EYMARD</creator><scope>EVB</scope></search><sort><creationdate>19810831</creationdate><title>Procédé de préparation de dérivés de polyols utiles en thérapeutique</title><author>CHARLES PIGEROL ; BERNARD FERRANDES ; MICHEL CHIGNAC ; CLAUDE GRAIN ; FERNAND JAMMOT ; PIERRE EYMARD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_OA6568A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>fre</language><creationdate>1981</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><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><topic>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</topic><toplevel>online_resources</toplevel><creatorcontrib>CHARLES PIGEROL</creatorcontrib><creatorcontrib>BERNARD FERRANDES</creatorcontrib><creatorcontrib>MICHEL CHIGNAC</creatorcontrib><creatorcontrib>CLAUDE GRAIN</creatorcontrib><creatorcontrib>FERNAND JAMMOT</creatorcontrib><creatorcontrib>PIERRE EYMARD</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>CHARLES PIGEROL</au><au>BERNARD FERRANDES</au><au>MICHEL CHIGNAC</au><au>CLAUDE GRAIN</au><au>FERNAND JAMMOT</au><au>PIERRE EYMARD</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Procédé de préparation de dérivés de polyols utiles en thérapeutique</title><date>1981-08-31</date><risdate>1981</risdate><abstract>Mono-, di-, tri- and tetra-esters derived from an acid of the general formula: R-OH in which R represents an acyl radical of the general formula: in which n represents 0 or 1, m represents 0, 1, 2, 3 or 4, R1 and R2 each represent a straight- or branched-chain alkyl radical having from 1 to 5 carbon atoms, R3 represents hydrogen or a straight- or branched-chain alkyl radical having from 1 to 5 carbon atoms, the sum of the carbon atoms in R1 and R2 being from 4 to 10 when R3 represents hydrogen and the sum of the carbon atoms in R1, R2 and R3 being from 6 to 15 when R3 is different from hydrogen, or R1 and R2 when they are taken together represent a tetramethylene, pentamethylene or hexamethylene radical and R3 represents a straight-chain alkyl radical and an alcohol selected from the group consisting of glycerol, 2,3-epoxy-propanol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,2,3-butanetriol, 1,2,4-butanetriol, 1,2,3,4-butanetetrol, 2-buten-1,4-diol, 2-butyn-1,4-diol, diethyleneglycol, a cyclohexanediol preferably 1,2-cyclohexanediol, thiodiglycol, diethanolamine, N-R-substituted-diethanolamine, trimethylolpropane, pentaerythritol and an alcohol of the general formula: II in which p represents 0 or 1, R4 represents methyl, R5 represents methyl, ethyl, 2-methyl-butyl or R4 and R5, when they are taken together represent a pentamethylene radical, with the exception of glyceryl tri-(di-n-propylacetate). These esters are useful in the treatment of central nervous system disorders and including, in particular, convulsive states and seizures, and disorders relating to the field of neuropsychiatry.</abstract><edition>3</edition><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS |
title | Procédé de préparation de dérivés de polyols utiles en thérapeutique |
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