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Synthesis and properties of 1,2-dihydropyridazino[4,5-b]indole II

Abstract

The possibility of the synthesis of substituted 1,2-dihydropyridazino[4,5-b]indoles by the reaction of 1-methyl-2-carbomethoxy-3-(α-halobenzyl)indole or 1-methyl-2-carbomethoxy-3-(α-acetoxybenzyl)indole with hydrazines was demonstrated. The oxidation, reduction, and acylation reactions of the resulting 1,2-dihydropyridazino[4,5-b]indoles were studied.

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See [3] for communication I.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 784–787, June, 1974.

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Vlasova, M.I., Kogan, N.A. Synthesis and properties of 1,2-dihydropyridazino[4,5-b]indole II. Chem Heterocycl Compd 10, 679–682 (1974). https://doi.org/10.1007/BF00480923

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Keywords

  • Oxidation
  • Organic Chemistry
  • Indole
  • Hydrazine
  • Acylation Reaction