Title of article
synthesis of novel 2-(alkyl/arylamino)-2-oxo-1- (quinolin-4-yl)ethyl cinnamates through three- component reaction between an isocyanide, quinoline-4-carbaldehyde and cinnamic acid derivatives
Author/Authors
taran, jafar university of zanjan - faculty of science - department of chemistry, zanjan, iran , ramazani, ali university of zanjan - faculty of science - department of chemistry, zanjan, iran , ramazani, ali university of zanjan - research institute of modern biological techniques (rimbt) - department of biotechnology, zanjan, iran
From page
319
To page
329
Abstract
passerini reactions of an isocyanide, quinoline-4- carbaldehyde, and cinnamic acid derivatives in water proceed at room temperature giving 2-(alkyl/aryl amino)-2-oxo-1- (quinolin-4- yl)ethyl cinnamate derivatives in quantitative yield. the reactions are one-pot, and the products did not require any purification. this procedure offers significant advantages such as operational simplicity, mild reaction conditions, enhanced rates, cleaner reaction profiles, ease of isolation of products, and h_2o as a medium, making it a valuable protocol for synthesizing these compounds.
Keywords
multicomponent reactions (mcrs) , passerini reactions , quinoline , 4 , carbaldehyde , isocyanide , cinnamic acid derivatives
Journal title
Eurasian Chemical Communications
Journal title
Eurasian Chemical Communications
Record number
2704911
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