Synthesis and Antiarrhythmic and Anticonvulsant Activities of Amino Amides and Amino Esters Based on 1-(4-Fluorophenyl)- and 1-[3-(Trifluoromethyl)phenyl]cyclopentane-1-carboxylic Acids

The alkylation of 2-(4-fluorophenyl)- and 2-[3-(trifluoromethyl)phenyl]acetonitriles with 1,4-di­bromo­butane gave 1-(substituted phenyl)cyclopentane-1-carbonitriles which were hydrolyzed to the corre­sponding carboxylic acids by the action of potassium hydroxide in ethylene glycol. The resulting ac...

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Vydáno v:Russian journal of organic chemistry Ročník 60; číslo 6; s. 1028 - 1035
Hlavní autoři: Arustamyan, J. S., Margaryan, R. E., Aghekyan, A. A., Mkrtchyan, G. S., Muradyan, R. E., Grigoryan, M. S., Panosyan, H. A., Mkryan, G. G.
Médium: Journal Article
Jazyk:angličtina
Vydáno: Moscow Pleiades Publishing 01.06.2024
PLEIADES PUBLISHING LTD
Springer Nature B.V
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ISSN:1070-4280, 1608-3393
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Shrnutí:The alkylation of 2-(4-fluorophenyl)- and 2-[3-(trifluoromethyl)phenyl]acetonitriles with 1,4-di­bromo­butane gave 1-(substituted phenyl)cyclopentane-1-carbonitriles which were hydrolyzed to the corre­sponding carboxylic acids by the action of potassium hydroxide in ethylene glycol. The resulting acids were converted to acid chlorides, and the latter reacted with N , N -dialkylaminoalkylamines, as well as with N , N -di­alkylaminoalkanols, to produce new amino amide and amino ester derivatives of 1-(4-fluorophenyl)- and 1-[3-(trifluoromethyl)phenyl]cyclopentane-1-carboxylic acids, which were characterized as hydrochlorides. The synthesized compounds were evaluated for their antiarrhythmic and anticonvulsant activities.
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ISSN:1070-4280
1608-3393
DOI:10.1134/S1070428024060071