Abstract
Aromatic carboxylic acids on refluxing with 3,5,6-trichloro-2-pyridyloxyacetylhydrazide in POCl3 gave 5-aryl-2-(3,5,6-trichloro-2-pyridyloxymethyl)-1,3,4-oxadiazoles. The hydrazide on treatment with acid chlorides gave diacylhydrazines, whereas with arylsulfonyl chlorides acyl(arylsulfonyl)hydrazines were obtained. The latter two types of compounds were tested for their antibacterial and antifungal activities whereas 1,3,4-oxadiazole derivatives were tested for their herbicidal activity.
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Published in Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 711–717, May, 2006.
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Chavan, V.P., Sonawane, S.A., Shingare, M.S. et al. Synthesis, characterization, and biological activities of some 3,5,6-trichloropyridine derivatives. Chem Heterocycl Compd 42, 625–630 (2006). https://doi.org/10.1007/s10593-006-0137-8
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DOI: https://doi.org/10.1007/s10593-006-0137-8