A convenient synthesis and cytotoxic activity of 3-aryl-5-pentyl-1,2,4- oxadiazoles from carboxylic acid esters and arylamidoximes under solvent-free conditions

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Abstract

The synthesis of 3-aryl-5-pentyl-1,2,4-oxadiazoles from carboxylic acid esters and arylamidoximes in the presence of potassium carbonate is described. The reaction was carried out in a microwave oven without any solvent in much shorter time and in good yields. The structures of the synthesized compounds were elucidated using IR, 1H and 13C NMR spectroscopy and elemental analysis and their antiproliferative activities was evaluated against three different human cell lines.

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Barros, C. J. P., De Souza, Z. C., De Freitas, J. J. R., Silva, P. B. N. D., Militão, G. C. G., Silva, T. G. D., … De Freitas Filho, J. R. (2014). A convenient synthesis and cytotoxic activity of 3-aryl-5-pentyl-1,2,4- oxadiazoles from carboxylic acid esters and arylamidoximes under solvent-free conditions. Journal of the Chilean Chemical Society, 59(1), 2359–2362. https://doi.org/10.4067/s0717-97072014000100024

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