DE1812417

1,187,340. Aminoalkyl ester of 4-benzylpiperidine-1-carboxylic acid. SOC. ANON. DES LABORATOIRES ROBERT ET CARRIERE. 5 Dec., 1968 [5 Dec., 1967; 30 Aug., 1968; 8 Oct., 1968], No. 57925/68. Heading C2C. Novel esters of formula wherein A is straight or branched alkylene, and R and R1 are each H, alkyl...

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Hauptverfasser: BUCHER, BERNARD PHILIPPE, PALAISEAU, ESSONE, CARRON, MAURICE CLAUDE ERNEST, CHATENAY-MALABRY, HAUTS DE SEINE, CARRON, CLAUDE LOUIS CLEMENT
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creator BUCHER, BERNARD PHILIPPE, PALAISEAU, ESSONE
CARRON, MAURICE CLAUDE ERNEST
CHATENAY-MALABRY, HAUTS DE SEINE
CARRON, CLAUDE LOUIS CLEMENT
description 1,187,340. Aminoalkyl ester of 4-benzylpiperidine-1-carboxylic acid. SOC. ANON. DES LABORATOIRES ROBERT ET CARRIERE. 5 Dec., 1968 [5 Dec., 1967; 30 Aug., 1968; 8 Oct., 1968], No. 57925/68. Heading C2C. Novel esters of formula wherein A is straight or branched alkylene, and R and R1 are each H, alkyl or aralkyl or together with the adjacent N form a monocyclic saturated heterocyclic radical, and acid addition salts, are prepared either by esterification of the acid chloride or ethyl ester with an alcohol of formula HO-A-N.R.R1, or by reaction of 4- benzyl-piperidine with a haloformate of formula X-COOA-Z where X is halogen and Z is halogen or -NRR1, followed where Z is halogen by reaction of the product with the amine HNRR1 and in both cases optionally followed by salt formation. 1 - Chloro - 2 - propyl 4 - benzylpiperidine - 1- carboxylate is prepared by reaction of 4-benzylpiperidine with 1-chloroisopropyl chloroformate. Pharmaceutical compositions in conventional forms for oral, rectal and parenteral administration comprise an above novel compound and a carrier or coating and are used in the treatment of disturbances of cardiac rhythm.
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Aminoalkyl ester of 4-benzylpiperidine-1-carboxylic acid. SOC. ANON. DES LABORATOIRES ROBERT ET CARRIERE. 5 Dec., 1968 [5 Dec., 1967; 30 Aug., 1968; 8 Oct., 1968], No. 57925/68. Heading C2C. Novel esters of formula wherein A is straight or branched alkylene, and R and R1 are each H, alkyl or aralkyl or together with the adjacent N form a monocyclic saturated heterocyclic radical, and acid addition salts, are prepared either by esterification of the acid chloride or ethyl ester with an alcohol of formula HO-A-N.R.R1, or by reaction of 4- benzyl-piperidine with a haloformate of formula X-COOA-Z where X is halogen and Z is halogen or -NRR1, followed where Z is halogen by reaction of the product with the amine HNRR1 and in both cases optionally followed by salt formation. 1 - Chloro - 2 - propyl 4 - benzylpiperidine - 1- carboxylate is prepared by reaction of 4-benzylpiperidine with 1-chloroisopropyl chloroformate. Pharmaceutical compositions in conventional forms for oral, rectal and parenteral administration comprise an above novel compound and a carrier or coating and are used in the treatment of disturbances of cardiac rhythm.</description><edition>1</edition><language>eng</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&amp;date=19740411&amp;DB=EPODOC&amp;CC=DE&amp;NR=1812417B2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19740411&amp;DB=EPODOC&amp;CC=DE&amp;NR=1812417B2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>BUCHER, BERNARD PHILIPPE, PALAISEAU, ESSONE</creatorcontrib><creatorcontrib>CARRON, MAURICE CLAUDE ERNEST</creatorcontrib><creatorcontrib>CHATENAY-MALABRY, HAUTS DE SEINE</creatorcontrib><creatorcontrib>CARRON, CLAUDE LOUIS CLEMENT</creatorcontrib><title>DE1812417</title><description>1,187,340. Aminoalkyl ester of 4-benzylpiperidine-1-carboxylic acid. SOC. ANON. DES LABORATOIRES ROBERT ET CARRIERE. 5 Dec., 1968 [5 Dec., 1967; 30 Aug., 1968; 8 Oct., 1968], No. 57925/68. Heading C2C. Novel esters of formula wherein A is straight or branched alkylene, and R and R1 are each H, alkyl or aralkyl or together with the adjacent N form a monocyclic saturated heterocyclic radical, and acid addition salts, are prepared either by esterification of the acid chloride or ethyl ester with an alcohol of formula HO-A-N.R.R1, or by reaction of 4- benzyl-piperidine with a haloformate of formula X-COOA-Z where X is halogen and Z is halogen or -NRR1, followed where Z is halogen by reaction of the product with the amine HNRR1 and in both cases optionally followed by salt formation. 1 - Chloro - 2 - propyl 4 - benzylpiperidine - 1- carboxylate is prepared by reaction of 4-benzylpiperidine with 1-chloroisopropyl chloroformate. Pharmaceutical compositions in conventional forms for oral, rectal and parenteral administration comprise an above novel compound and a carrier or coating and are used in the treatment of disturbances of cardiac rhythm.</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>eNrjZOB0cTW0MDQyMTTnYWBNS8wpTuWF0twMCm6uIc4euqkF-fGpxQWJyal5qSXxcPVORsZEKAEAyskaZQ</recordid><startdate>19740411</startdate><enddate>19740411</enddate><creator>BUCHER, BERNARD PHILIPPE, PALAISEAU, ESSONE</creator><creator>CARRON, MAURICE CLAUDE ERNEST</creator><creator>CHATENAY-MALABRY, HAUTS DE SEINE</creator><creator>CARRON, CLAUDE LOUIS CLEMENT</creator><scope>EVB</scope></search><sort><creationdate>19740411</creationdate><title>DE1812417</title><author>BUCHER, BERNARD PHILIPPE, PALAISEAU, ESSONE ; CARRON, MAURICE CLAUDE ERNEST ; CHATENAY-MALABRY, HAUTS DE SEINE ; CARRON, CLAUDE LOUIS CLEMENT</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE1812417B23</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1974</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>BUCHER, BERNARD PHILIPPE, PALAISEAU, ESSONE</creatorcontrib><creatorcontrib>CARRON, MAURICE CLAUDE ERNEST</creatorcontrib><creatorcontrib>CHATENAY-MALABRY, HAUTS DE SEINE</creatorcontrib><creatorcontrib>CARRON, CLAUDE LOUIS CLEMENT</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>BUCHER, BERNARD PHILIPPE, PALAISEAU, ESSONE</au><au>CARRON, MAURICE CLAUDE ERNEST</au><au>CHATENAY-MALABRY, HAUTS DE SEINE</au><au>CARRON, CLAUDE LOUIS CLEMENT</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>DE1812417</title><date>1974-04-11</date><risdate>1974</risdate><abstract>1,187,340. Aminoalkyl ester of 4-benzylpiperidine-1-carboxylic acid. SOC. ANON. DES LABORATOIRES ROBERT ET CARRIERE. 5 Dec., 1968 [5 Dec., 1967; 30 Aug., 1968; 8 Oct., 1968], No. 57925/68. Heading C2C. Novel esters of formula wherein A is straight or branched alkylene, and R and R1 are each H, alkyl or aralkyl or together with the adjacent N form a monocyclic saturated heterocyclic radical, and acid addition salts, are prepared either by esterification of the acid chloride or ethyl ester with an alcohol of formula HO-A-N.R.R1, or by reaction of 4- benzyl-piperidine with a haloformate of formula X-COOA-Z where X is halogen and Z is halogen or -NRR1, followed where Z is halogen by reaction of the product with the amine HNRR1 and in both cases optionally followed by salt formation. 1 - Chloro - 2 - propyl 4 - benzylpiperidine - 1- carboxylate is prepared by reaction of 4-benzylpiperidine with 1-chloroisopropyl chloroformate. Pharmaceutical compositions in conventional forms for oral, rectal and parenteral administration comprise an above novel compound and a carrier or coating and are used in the treatment of disturbances of cardiac rhythm.</abstract><edition>1</edition><oa>free_for_read</oa></addata></record>
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HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title DE1812417
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