METHOD OF PREPARING 1,4-DIHYDROPYRIDINECARBOXYLIC ACID ARALALKYL ESTERS

1,4-Dihydropyridines characterized by a carbo(arylalkoxy) group in the 5-position, an aryl group in the 4-position and a alkanoyl or carbalkoxy group in the 3-position and further optionally substituted in the 1,2 and 6-positions are coronary dilating, spasmolytic and hypotensive agents. The compoun...

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Hauptverfasser: FRIDRIKH BOSSERT,DT, STANISLAV KATSDA,DT, EGBERT VEKHINGER,DT, KURT SHTEPEL,DT, VULF FATER,DT
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creator FRIDRIKH BOSSERT,DT
STANISLAV KATSDA,DT
EGBERT VEKHINGER,DT
KURT SHTEPEL,DT
VULF FATER,DT
description 1,4-Dihydropyridines characterized by a carbo(arylalkoxy) group in the 5-position, an aryl group in the 4-position and a alkanoyl or carbalkoxy group in the 3-position and further optionally substituted in the 1,2 and 6-positions are coronary dilating, spasmolytic and hypotensive agents. The compounds, of which 2,6-dimethyl-3-carbomethoxy-4-(2-nitrophenyl)-5-carbobenzoxy-1,4-dihyd ropyridine is a representative embodiment, are prepared through the reaction of an ylidene- beta -dicarbonyl compound, which may be generated in situ from the corresponding beta -dicarbonyl compound and an aldehyde, and an enaminocarboxylic acid ester, which may also be generated in situ from a beta -dicarbonyl compound and an amine.
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The compounds, of which 2,6-dimethyl-3-carbomethoxy-4-(2-nitrophenyl)-5-carbobenzoxy-1,4-dihyd ropyridine is a representative embodiment, are prepared through the reaction of an ylidene- beta -dicarbonyl compound, which may be generated in situ from the corresponding beta -dicarbonyl compound and an aldehyde, and an enaminocarboxylic acid ester, which may also be generated in situ from a beta -dicarbonyl compound and an amine.</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 ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</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=19770925&amp;DB=EPODOC&amp;CC=SU&amp;NR=574150A3$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19770925&amp;DB=EPODOC&amp;CC=SU&amp;NR=574150A3$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>FRIDRIKH BOSSERT,DT</creatorcontrib><creatorcontrib>STANISLAV KATSDA,DT</creatorcontrib><creatorcontrib>EGBERT VEKHINGER,DT</creatorcontrib><creatorcontrib>KURT SHTEPEL,DT</creatorcontrib><creatorcontrib>VULF FATER,DT</creatorcontrib><title>METHOD OF PREPARING 1,4-DIHYDROPYRIDINECARBOXYLIC ACID ARALALKYL ESTERS</title><description>1,4-Dihydropyridines characterized by a carbo(arylalkoxy) group in the 5-position, an aryl group in the 4-position and a alkanoyl or carbalkoxy group in the 3-position and further optionally substituted in the 1,2 and 6-positions are coronary dilating, spasmolytic and hypotensive agents. 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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
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title METHOD OF PREPARING 1,4-DIHYDROPYRIDINECARBOXYLIC ACID ARALALKYL ESTERS
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