CARBOXYLIC ACID AMIDES A PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS

New carboxamides of formula (I): (where R1-3=same or different, saturated or unsaturated, straight branched or cyclic hydrocarbyl the carbon chain of which may be interrupted by heteroatoms or divalent groups e.g. O,S, -SO-, -SO2-, -CO- or phenylene and may be substituted by substituents such as hal...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: LINKE S, SITT R
Format: Patent
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator LINKE S
SITT R
description New carboxamides of formula (I): (where R1-3=same or different, saturated or unsaturated, straight branched or cyclic hydrocarbyl the carbon chain of which may be interrupted by heteroatoms or divalent groups e.g. O,S, -SO-, -SO2-, -CO- or phenylene and may be substituted by substituents such as halo, alkoxy, acyloxy, aryl, aryloxy, arylmercapto, aroyl, alkylmercapto, alkylsulphenyl, alkylsulphonyl, acylamino, aroylamino, cyano, alkoxycarbonyl, aryloxycarbonyl or carbamoyl (opt. substd. by alkyl); R4,R5=same or different H, opt. substd. aryl or saturated or unsaturated, straight, branched or cyclic hydrocarbyl the carbon chain of which is opt. interrupted by heteroatoms or groups such as O,S,SO2,SO,CO and phenylene and may be substd. by hydroxy, alkoxy, halo, acyloxy, acylamino, aryl, aryloxy, aroyl, alkylmercapto, alkylsulphonyl, alkylsulphinyl, cyano, alkoxycarbonyl, aryloxycarbonyl or carbamoul (opt. substd. by alkyl or aryl) radicals or R4 and R5 together may form an alkylene chain; when n=0, R4 and R5 together = alkylene thus form a heterocyclic containing the two N atoms; X=saturated or unsaturated, straight, branched or cyclic hydrocarbon chain which may be interrupted by heteroatoms or groups such as O,S,SO,SO2, arylaza, alkylaza, carbonyl or phenylene and may be substd. by halo, alkoxy, aryloxy, hydroxy, cyano, carboxy, carbalkoxy, acylamino, carbaryloxy, alkylmercapto, alkylsulphinyl, alkylsulphonyl, arylmercapto, aryl or carbamoyl (opt. substd. by alkyl or aryl), radicals and n=0-4. All aryl radicals defined in R1-5 and X have 6-10C atoms and are opt. substd. (I) are hypolipemics which reduce hyperlipemia and the absorption of cholesterol and is administered orally, parenthelly or rectally in the treatment of lipid metabolism troubles e.g. adiposity and hyperlipoproteinemia. The cpds. have low toxicity oral LD50 in mice >2000mg/kg.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_ZA762088B</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ZA762088B</sourcerecordid><originalsourceid>FETCH-epo_espacenet_ZA762088B3</originalsourceid><addsrcrecordid>eNrjZAh2dgxy8o-I9PF0VnB09nRRcPT1dHENVnBUCAjyd3YNDlZw8w9SCPFw9QwCirgGOAY5hnj6-yk4-rlARUODXRUcgxV8XV08nR19Xf1CgnkYWNMSc4pTeaE0N4Ocm2uIs4duakF-fGpxQWJyal5qSXyUo7mZkYGFhZMxQQUAufsuXg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>CARBOXYLIC ACID AMIDES A PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS</title><source>esp@cenet</source><creator>LINKE S ; SITT R</creator><creatorcontrib>LINKE S ; SITT R</creatorcontrib><description>New carboxamides of formula (I): (where R1-3=same or different, saturated or unsaturated, straight branched or cyclic hydrocarbyl the carbon chain of which may be interrupted by heteroatoms or divalent groups e.g. O,S, -SO-, -SO2-, -CO- or phenylene and may be substituted by substituents such as halo, alkoxy, acyloxy, aryl, aryloxy, arylmercapto, aroyl, alkylmercapto, alkylsulphenyl, alkylsulphonyl, acylamino, aroylamino, cyano, alkoxycarbonyl, aryloxycarbonyl or carbamoyl (opt. substd. by alkyl); R4,R5=same or different H, opt. substd. aryl or saturated or unsaturated, straight, branched or cyclic hydrocarbyl the carbon chain of which is opt. interrupted by heteroatoms or groups such as O,S,SO2,SO,CO and phenylene and may be substd. by hydroxy, alkoxy, halo, acyloxy, acylamino, aryl, aryloxy, aroyl, alkylmercapto, alkylsulphonyl, alkylsulphinyl, cyano, alkoxycarbonyl, aryloxycarbonyl or carbamoul (opt. substd. by alkyl or aryl) radicals or R4 and R5 together may form an alkylene chain; when n=0, R4 and R5 together = alkylene thus form a heterocyclic containing the two N atoms; X=saturated or unsaturated, straight, branched or cyclic hydrocarbon chain which may be interrupted by heteroatoms or groups such as O,S,SO,SO2, arylaza, alkylaza, carbonyl or phenylene and may be substd. by halo, alkoxy, aryloxy, hydroxy, cyano, carboxy, carbalkoxy, acylamino, carbaryloxy, alkylmercapto, alkylsulphinyl, alkylsulphonyl, arylmercapto, aryl or carbamoyl (opt. substd. by alkyl or aryl), radicals and n=0-4. All aryl radicals defined in R1-5 and X have 6-10C atoms and are opt. substd. (I) are hypolipemics which reduce hyperlipemia and the absorption of cholesterol and is administered orally, parenthelly or rectally in the treatment of lipid metabolism troubles e.g. adiposity and hyperlipoproteinemia. The cpds. have low toxicity oral LD50 in mice &gt;2000mg/kg.</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1977</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=19770427&amp;DB=EPODOC&amp;CC=ZA&amp;NR=762088B$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19770427&amp;DB=EPODOC&amp;CC=ZA&amp;NR=762088B$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>LINKE S</creatorcontrib><creatorcontrib>SITT R</creatorcontrib><title>CARBOXYLIC ACID AMIDES A PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS</title><description>New carboxamides of formula (I): (where R1-3=same or different, saturated or unsaturated, straight branched or cyclic hydrocarbyl the carbon chain of which may be interrupted by heteroatoms or divalent groups e.g. O,S, -SO-, -SO2-, -CO- or phenylene and may be substituted by substituents such as halo, alkoxy, acyloxy, aryl, aryloxy, arylmercapto, aroyl, alkylmercapto, alkylsulphenyl, alkylsulphonyl, acylamino, aroylamino, cyano, alkoxycarbonyl, aryloxycarbonyl or carbamoyl (opt. substd. by alkyl); R4,R5=same or different H, opt. substd. aryl or saturated or unsaturated, straight, branched or cyclic hydrocarbyl the carbon chain of which is opt. interrupted by heteroatoms or groups such as O,S,SO2,SO,CO and phenylene and may be substd. by hydroxy, alkoxy, halo, acyloxy, acylamino, aryl, aryloxy, aroyl, alkylmercapto, alkylsulphonyl, alkylsulphinyl, cyano, alkoxycarbonyl, aryloxycarbonyl or carbamoul (opt. substd. by alkyl or aryl) radicals or R4 and R5 together may form an alkylene chain; when n=0, R4 and R5 together = alkylene thus form a heterocyclic containing the two N atoms; X=saturated or unsaturated, straight, branched or cyclic hydrocarbon chain which may be interrupted by heteroatoms or groups such as O,S,SO,SO2, arylaza, alkylaza, carbonyl or phenylene and may be substd. by halo, alkoxy, aryloxy, hydroxy, cyano, carboxy, carbalkoxy, acylamino, carbaryloxy, alkylmercapto, alkylsulphinyl, alkylsulphonyl, arylmercapto, aryl or carbamoyl (opt. substd. by alkyl or aryl), radicals and n=0-4. All aryl radicals defined in R1-5 and X have 6-10C atoms and are opt. substd. (I) are hypolipemics which reduce hyperlipemia and the absorption of cholesterol and is administered orally, parenthelly or rectally in the treatment of lipid metabolism troubles e.g. adiposity and hyperlipoproteinemia. The cpds. have low toxicity oral LD50 in mice &gt;2000mg/kg.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1977</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZAh2dgxy8o-I9PF0VnB09nRRcPT1dHENVnBUCAjyd3YNDlZw8w9SCPFw9QwCirgGOAY5hnj6-yk4-rlARUODXRUcgxV8XV08nR19Xf1CgnkYWNMSc4pTeaE0N4Ocm2uIs4duakF-fGpxQWJyal5qSXyUo7mZkYGFhZMxQQUAufsuXg</recordid><startdate>19770427</startdate><enddate>19770427</enddate><creator>LINKE S</creator><creator>SITT R</creator><scope>EVB</scope></search><sort><creationdate>19770427</creationdate><title>CARBOXYLIC ACID AMIDES A PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS</title><author>LINKE S ; SITT R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_ZA762088B3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1977</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>LINKE S</creatorcontrib><creatorcontrib>SITT R</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>LINKE S</au><au>SITT R</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>CARBOXYLIC ACID AMIDES A PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS</title><date>1977-04-27</date><risdate>1977</risdate><abstract>New carboxamides of formula (I): (where R1-3=same or different, saturated or unsaturated, straight branched or cyclic hydrocarbyl the carbon chain of which may be interrupted by heteroatoms or divalent groups e.g. O,S, -SO-, -SO2-, -CO- or phenylene and may be substituted by substituents such as halo, alkoxy, acyloxy, aryl, aryloxy, arylmercapto, aroyl, alkylmercapto, alkylsulphenyl, alkylsulphonyl, acylamino, aroylamino, cyano, alkoxycarbonyl, aryloxycarbonyl or carbamoyl (opt. substd. by alkyl); R4,R5=same or different H, opt. substd. aryl or saturated or unsaturated, straight, branched or cyclic hydrocarbyl the carbon chain of which is opt. interrupted by heteroatoms or groups such as O,S,SO2,SO,CO and phenylene and may be substd. by hydroxy, alkoxy, halo, acyloxy, acylamino, aryl, aryloxy, aroyl, alkylmercapto, alkylsulphonyl, alkylsulphinyl, cyano, alkoxycarbonyl, aryloxycarbonyl or carbamoul (opt. substd. by alkyl or aryl) radicals or R4 and R5 together may form an alkylene chain; when n=0, R4 and R5 together = alkylene thus form a heterocyclic containing the two N atoms; X=saturated or unsaturated, straight, branched or cyclic hydrocarbon chain which may be interrupted by heteroatoms or groups such as O,S,SO,SO2, arylaza, alkylaza, carbonyl or phenylene and may be substd. by halo, alkoxy, aryloxy, hydroxy, cyano, carboxy, carbalkoxy, acylamino, carbaryloxy, alkylmercapto, alkylsulphinyl, alkylsulphonyl, arylmercapto, aryl or carbamoyl (opt. substd. by alkyl or aryl), radicals and n=0-4. All aryl radicals defined in R1-5 and X have 6-10C atoms and are opt. substd. (I) are hypolipemics which reduce hyperlipemia and the absorption of cholesterol and is administered orally, parenthelly or rectally in the treatment of lipid metabolism troubles e.g. adiposity and hyperlipoproteinemia. The cpds. have low toxicity oral LD50 in mice &gt;2000mg/kg.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_ZA762088B
source esp@cenet
subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title CARBOXYLIC ACID AMIDES A PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T04%3A34%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=LINKE%20S&rft.date=1977-04-27&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EZA762088B%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true