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Indolopyridines with a hetero atom at a position of fusion. 7. Electrophilic substitution in 5,6-dihydroindolo-[2,1-a]isoquinoline

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Halogenation, acylation, azo coupling, and alkylaminomethylation of 5,6-dihydroindoto[2,I-alisoguinoline were carried out at the C(11) position (pyrrole fragment). In dibromination, the second bromine atom was introduced into the C(9) position (indole part of the molecule).

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References

  1. G. Ntaganda, S. A. Soldatova, J. A. R. Alarcon, B. N. Anisimov, and A. T. Soldatenkov, Khim. Geterotsikl. Soedin., No. 1, 83 (1994).

  2. J. A. R. Alarcon, S. A. Soldatova, A. T. Soldatenkov, M. A. Ryashentseva, and N. S. Prostakov, Izv. Akad. Nauk SSSR, Ser. Khim., No. 6, 1413 (1991).

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Authors and Affiliations

  1. Russian Peoples' Friendship University, 117923, Moscow

    G. Ntaganda, S. A. Soldatova, B. N. Anisimov, J. A. R. Alarcon & A. T. Soldatenkov

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  1. G. Ntaganda
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  2. S. A. Soldatova
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  3. B. N. Anisimov
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  4. J. A. R. Alarcon
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  5. A. T. Soldatenkov
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 217–220, February, 1994. Original article submitted November 19, 1993.

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Ntaganda, G., Soldatova, S.A., Anisimov, B.N. et al. Indolopyridines with a hetero atom at a position of fusion. 7. Electrophilic substitution in 5,6-dihydroindolo-[2,1-a]isoquinoline. Chem Heterocycl Compd 30, 196–199 (1994). https://doi.org/10.1007/BF01165011

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  • DOI: https://doi.org/10.1007/BF01165011

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