Abstract
Three-component reaction of substituted benzoyl chlorides, ammonium thiocyanate, and isatin in anhydrous acetone gave a series of novel N-(2,3-dioxo-2,3-dihydro-1H-indole-1-carbothioyl)benzamides, and condensation of the latter with hydrazine hydrate in anhydrous ethanol under reflux afforded 1-(5-(aryl)-4H-1,2,4-triazol-3-yl)-2,3-dihydro-1H-indole-2,3-dione derivatives. The structure of the synthesized compounds was confirmed by elemental analyses and FT-IR and 1H and 13C NMR data.
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Afshar, N., Hatamjafari, F., Shiroudi, A. et al. Synthesis and Characterization of Some New Indoline-Based 1,2,4-Triazole Derivatives. Russ J Org Chem 56, 2153–2158 (2020). https://doi.org/10.1134/S1070428020120179
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DOI: https://doi.org/10.1134/S1070428020120179