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The chemistry of indole

XII. 2-Aminoindoles and pyrimidyl[l, 2-β]indoles

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The synthesis of 2-aminoindoles substituted in the benzene ring is described. On the basis of a study of the PMR, UV, and IR spectra their salts have been ascribed the structure of indolenine derivatives. A number of pyrimidyl[l, 2-a]indoles have been obtained from 2-aminoindoles and acetylacetone.

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References

  1. A. N. Kost, R. S. Sagitullin, V. I. Gorbunov, and N. N. Modyanov, KhGS [Chemistry of Heterocyclic Compounds], 6, 359, 1970.

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Authors and Affiliations

  1. Moscow State University, USSR

    R. S. Sagitullin, V. I. Gorbunov, A. N. Kost, N. B. Kuplet-skaya & V. V. Chistyakov

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  1. R. S. Sagitullin
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  2. V. I. Gorbunov
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  3. A. N. Kost
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  4. N. B. Kuplet-skaya
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  5. V. V. Chistyakov
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Additional information

For part XI, see [1].

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Sagitullin, R.S., Gorbunov, V.I., Kost, A.N. et al. The chemistry of indole. Chem Heterocycl Compd 6, 338–343 (1970). https://doi.org/10.1007/BF00471237

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  • DOI: https://doi.org/10.1007/BF00471237

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