Abstract
2,5-Disubstituted oxadiazoles with indole residues were synthesized by condensation of the hydrochlorides of the corresponding imido esters with hydrazines, as well as by cyclization of hydrazides by the action of POCl3. 2-Substituted oxadiazoles of the same series were obtained by condensation of the corresponding hydrazides with ethyl orthoformate.
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V. I. Kelarev and G. A. Shvekhgeimer, Khim. Geterotsikl. Soedin., No. 5, 645 (1980).
E. P. Nesynov and A. P. Grekov, Usp. Khim., 33, 1188 (1964).
C. Ainsworth and R. E. Hackler, J. Org. Chem., 31, 3442 (1966).
A. R. Katritzky, Physical Methods in the Chemistry of Heterocyclic Compounds, Academic Press (1963).
J. Imai, Makromol. Chem., 83, 170 (1965).
R. L. Sundberg, The Chemistry of Indoles, New York (1970), p. 21.
H. L. Yalle, K. Losee, J. Martins, M. Holsing, F. M. Perry, and J. Bernstein, J. Am. Chem. Soc., 75, 1937 (1953).
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See [1] for Communication 32.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 343–347, March, 1982.
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Kelarev, V.I., Shvekhgeimer, G.A. Synthesis and properties of azoles and their derivatives. 33. Synthesis of 1,3,4-oxadiazoles that contain an indolyl group. Chem Heterocycl Compd 18, 258–261 (1982). https://doi.org/10.1007/BF00522123
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DOI: https://doi.org/10.1007/BF00522123