Ruthenium-catalyzed C3 Alkylation of the Furan/Thiophene Ring in 2-(Furan-2-carbonyl)/(Thiophene-2-carbonyl)-1-methylimidazoles with Acrylic Acid Derivatives

A method for the synthesis of 3-alkyl-2-(furan-2-carbonyl)/(thiophene-2-carbonyl)-1-methylimidazoles by the ruthenium-catalyzed selective C3 alkylation of the furan or thiophene ring in 2-(furan-2-carbonyl)/(thiophene-2-carbonyl)-1-methylimidazoles with acrylic acid esters, amides, or nitrile has been developed. The resulting compounds may be of interest as polyfunctional reagents for preparing 3-(2-carboxyethyl)furan/thiophene-2-carboxylic acid derivatives.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2024-11-01
DOI
https://doi.org/10.1134/s1070428024110071
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Ruthenium-catalyzed C3 Alkylation of the Furan/Thiophene Ring in 2-(Furan-2-carbonyl)/(Thiophene-2-carbonyl)-1-methylimidazoles with Acrylic Acid Derivatives

Irina G. Gnatiuk, Konstantin E. Shepelenko, Victor M. Chernyshev
2 citations
Russian Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.50
article

Ruthenium-catalyzed C3 Alkylation of the Furan/Thiophene Ring in 2-(Furan-2-carbonyl)/(Thiophene-2-carbonyl)-1-methylimidazoles with Acrylic Acid Derivatives

Irina G. Gnatiuk, Konstantin E. Shepelenko, Victor M. Chernyshev
article en
2 citations

Abstract

A method for the synthesis of 3-alkyl-2-(furan-2-carbonyl)/(thiophene-2-carbonyl)-1-methylimidazoles by the ruthenium-catalyzed selective C3 alkylation of the furan or thiophene ring in 2-(furan-2-carbonyl)/(thiophene-2-carbonyl)-1-methylimidazoles with acrylic acid esters, amides, or nitrile has been developed. The resulting compounds may be of interest as polyfunctional reagents for preparing 3-(2-carboxyethyl)furan/thiophene-2-carboxylic acid derivatives.

Russian Journal of Organic ChemistryVol. 60(11)
Platov South-Russian State Polytechnic University (RU)
Openalex Percentile: Top 37%
Catalytic C–H Functionalization Methods
0.50
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