Abstract
The reaction of pyrroloquinoline with N-acylpyridinium, N-acylquinolinium, N-acylisoquinolinium, and N-acylbenzimidazolium salts (formed as a result of the reaction with carboxylic acid chlorides), which leads to partially hydrogenated N-acyl derivatives of pyrroloquinoline, was investigated. The reaction of pyrroloquino-line with acridine hydrochloride, as a result of which its acridine derivative was obtained, was carried out.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 251–254, February, 1978.
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Stupnikova, T.V., Sheinkman, A.K., Rybenko, L.A. et al. Reaction of 2-methylpyrrolo[3,2-H]quinoline with N-acyl salts of heteroaromatic cations in situ. Chem Heterocycl Compd 14, 204–207 (1978). https://doi.org/10.1007/BF00945336
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DOI: https://doi.org/10.1007/BF00945336