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Synthesis and properties of azoles and their derivatives. 33. Synthesis of 1,3,4-oxadiazoles that contain an indolyl group

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Chemistry of Heterocyclic Compounds Aims and scope

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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Literature cited

  1. V. I. Kelarev and G. A. Shvekhgeimer, Khim. Geterotsikl. Soedin., No. 5, 645 (1980).

    Google Scholar 

  2. E. P. Nesynov and A. P. Grekov, Usp. Khim., 33, 1188 (1964).

    Google Scholar 

  3. C. Ainsworth and R. E. Hackler, J. Org. Chem., 31, 3442 (1966).

    Google Scholar 

  4. A. R. Katritzky, Physical Methods in the Chemistry of Heterocyclic Compounds, Academic Press (1963).

  5. J. Imai, Makromol. Chem., 83, 170 (1965).

    Google Scholar 

  6. R. L. Sundberg, The Chemistry of Indoles, New York (1970), p. 21.

  7. H. L. Yalle, K. Losee, J. Martins, M. Holsing, F. M. Perry, and J. Bernstein, J. Am. Chem. Soc., 75, 1937 (1953).

    Google Scholar 

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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

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