Abstract
3-Aminoindole was obtained by the action of alkali on its hydrochloride in a reductive medium. Acylation of 3-aminoindole with acetic anhydride gave its mono-, di-, and triacetyl derivatives, whereas reaction with p-substituted benzenesulfonyl chlorides gave the corresponding N-3-indolylsulfonamides. The reaction of 3-aminoindole with aromatic aldehydes gives Schiff bases.
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See [1] for communication CXII.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 481–485, April, 1977.
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Yarosh, A.V., Velezheva, V.S., Kozik, T.A. et al. Indole derivatives. Chem Heterocycl Compd 13, 386–390 (1977). https://doi.org/10.1007/BF00482780
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DOI: https://doi.org/10.1007/BF00482780