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Synthesis of Pyrrolo[a]- and Pyrrolo[c]phenanthridine Derivatives and Indolinyl and Indolylsubstituted 6-Phenanthridines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The corresponding Mannich bases have been synthesized by the aminomethylation of 6-methyl-1H-pyrrolo[2,3-a]- and 4-methyl-3H-pyrrolo[3,2-c]phenanthridinium iodides. The interaction of 6-chloro-phenanthridine with indoline and with 5-amino-N-acetylindoline gave the corresponding derivatives of phenanthridine. 6-(1-Indolyl)phenanthridine has been obtained by the dehydrogenation of 6-(1-indolinyl)phenanthridine with manganese dioxide.

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Authors and Affiliations

  1. Russian University of Chemical Technology, Moscow, 125190

    E. P. Baberkina, V. N. Buyanov, M. E. Zhukova, A. E. Shchekotikhin, V. E. Zhigachev & N. N. Suvorov

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  1. E. P. Baberkina
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  2. V. N. Buyanov
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  3. M. E. Zhukova
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  4. A. E. Shchekotikhin
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  5. V. E. Zhigachev
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  6. N. N. Suvorov
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Baberkina, E.P., Buyanov, V.N., Zhukova, M.E. et al. Synthesis of Pyrrolo[a]- and Pyrrolo[c]phenanthridine Derivatives and Indolinyl and Indolylsubstituted 6-Phenanthridines. Chemistry of Heterocyclic Compounds 37, 1234–1237 (2001). https://doi.org/10.1023/A:1013897410464

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  • DOI: https://doi.org/10.1023/A:1013897410464

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