Synthesis and Antiinflammatory Activity of 3-Aryl-5-Isopropyl-1,2,4-Oxadiazoles

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Abstract

Seven 4,5-dihydro-1,2,4-oxadiazoles 3a-g have been synthesized from arylamidoximes 1a-g and isobutyraldehyde 2 in the presence of an acid catalyst (IRP-64). Oxidation of 3a-g either with MnO2 or with nitric acid provided 4a-g. Compounds 3b,c,f,g and 4b,c,e-g have not been reported in the literature. All seven oxadiazoles 4a-g showed antiinflammatory activity.

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Srivastava, R. M., De Morais, L. P. F., Catanho, M. T. J. A., De Souza, G. M. L., Seabra, G. M., Simas, A. M., & Rodrigues, M. A. L. (2000). Synthesis and Antiinflammatory Activity of 3-Aryl-5-Isopropyl-1,2,4-Oxadiazoles. Heterocyclic Communications, 6(1), 41–48. https://doi.org/10.1515/HC.2000.6.1.41

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