Abstract
Isochromylium cations containing easily detached groupings (NHCOR, NH2, OCH3) in the 3 position react readily with o-phenylenediamine. The reaction is accompanied by opening of the benzopyrylium ring and condensation of the resulting compound at one or two amino groups of o-phenylenediamine. Benzimidazo[3,2-b]isoquinolinium salts were synthesized alternatively by acylation of 2-(3,4-dimethoxybenzyl)benzimidazole. The tautomerism of the synthesized N-(2-aminoaryl)isoquinolinium perchlorates was investigated.
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See [1] for communication II.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 238–243, February, 1976.
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Andreichikov, Y.P., Trukhan, G.E., Lyubchenko, S.N. et al. Condensed heterocyclic systems with a quaternary nitrogen atom. III. Synthesis of benzimidazo[3,2-b]isoquinolinium perchlorates. Chem Heterocycl Compd 12, 205–210 (1976). https://doi.org/10.1007/BF00523972
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DOI: https://doi.org/10.1007/BF00523972