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N-acetylindoxyl in the synthesis of new condensed heterocycles

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Derivatives of a new heterocyclic system thieno[2′,3′∶5,6]pyrimido[3,4-a]indole, were obtained by the reaction of substituted N,O-diacetylindoxyls with excess N-(2-methyl-3-ethoxycarbonyl-4-thienyl)hydrazine. The reaction of N-acetylindoxyl and 4-hydrazinouracil forms 12-amino-1,3-dioxo-2,4,6-trimethylpyrimido[5′,4′∶5,6]pyrimido[3,4-a]indole.

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Literature Cited

  1. G. N. Kurilo, S. Yu. Ryabova, and A. N. Grinev, Khim. Geterotsikl. Soedin., No. 6, 832 (1979).

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  2. A. N. Grinev, N. N. Suvorov, S. Yu. Ryabova, G. N. Kurilo, K. F. Turchin, and V. S. Velezheva, Khim. Geterotsikl. Soedin., No. 11, 1486 (1979).

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Deceased.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, 1343–1345, October, 1987.

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Ryabova, S.Y., Grinev, A.N. & Kurilo, G.N. N-acetylindoxyl in the synthesis of new condensed heterocycles. Chem Heterocycl Compd 23, 1076–1078 (1987). https://doi.org/10.1007/BF00476535

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  • DOI: https://doi.org/10.1007/BF00476535

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