Synthesis of some 1- and 2-carboxyalkyl substituted benzimidazoles and their derivatives

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Abstract

Mono- and disubstituted benzimidazoles were synthesized during alkaline hydrolysis or reactions with ethyl chloroacetate of 1-phenyl substituted 4-(1H-benzimidazol-2-yl)-2-pyrrolidinones. The properties of the synthesized ethyl-[2-(1-(substituted phenyl)-5-oxopyrrolidinyl-3-yl)-1H-benzimidazolyl] ethanoates have been investigated and their benzimidazolium chlorides, 1-carboxymethylbenzimidazoles, condensation products of 2-{2-[1-(3-methylphenyl) -5-oxo-3-pyrrolidinyl]-1H-benzimidazol-1-yl}acetohydrazide with various aromatic aldehydes and aliphatic ketones have been obtained. © 2013 The Author(s).

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Mickevičienė, K., Voskienė, A., & Mickevičius, V. (2014). Synthesis of some 1- and 2-carboxyalkyl substituted benzimidazoles and their derivatives. Research on Chemical Intermediates, 40(4), 1619–1631. https://doi.org/10.1007/s11164-013-1067-6

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