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Scheme 1 | Chemistry Central Journal

Scheme 1

From: Synthesis, characterization, biological evaluation and molecular docking studies of 2-(1H-benzo[d]imidazol-2-ylthio)-N-(substituted 4-oxothiazolidin-3-yl) acetamides

Scheme 1

Scheme for synthesis of benzimidazole-substituted-1,3-thiazolidin-4-ones. Reaction conditions: (i) Ethanol, ethyl chloroacetate, stirring for 24 h. (ii) Ethanol, hydrazine hydrate, reflux. (iii) Aryl aldehyde, ethanol, a few drops of glacial acetic acid. (iv) Cinnamaldehyde, ethanol, a few drops of glacial acetic acid. (v) 4-Hydroxy-naphthaldehyde, ethanol, a few drops of glacial acetic acid. (vi) Dioxane, thioglycolic acid, anhydrous zinc chloride, reflux

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