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Synthesis of 10-phthalimidoalkyltetrahydropyrimido[1,2-a]-indoles

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

10-Phthalimidoalkyltetrahydropyrimido [1,2-a] indoles were obtained by rearrangement of cyclic hydrazides of N-phthalyl-ω-amino acids, viz., 1-phenyl-2-acyl-pyrazolidines, under the influence of phosphorus oxychloride.

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Literature cited

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Authors and Affiliations

  1. Branch of the S. Ordzhonikidze All-Union Scientific-Research Institute of Pharmaceutical Chemistry, 142450, Kupavna

    Yu. N. Portnov, V. G. Voronin & V. G. Zabrodnyaya

Authors
  1. Yu. N. Portnov
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  2. V. G. Voronin
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  3. V. G. Zabrodnyaya
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1081–1083, August, 1985.

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Portnov, Y.N., Voronin, V.G. & Zabrodnyaya, V.G. Synthesis of 10-phthalimidoalkyltetrahydropyrimido[1,2-a]-indoles. Chem Heterocycl Compd 21, 902–904 (1985). https://doi.org/10.1007/BF00519819

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  • DOI: https://doi.org/10.1007/BF00519819

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