Chemistry of indole XLIII. New synthesis of benz(aminomethyl)indoles |
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| Authors: | A. N. Kost L. G. Yudin M. Abdullaev |
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| Affiliation: | 1. Andizhan State Pedagogical Institute, M. V. Lomonosov Moscow State University, USSR
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| Abstract: | Indolines are amidomethylated in the 6 position in acidic media. N-Acetylation changes the orientation to give the 5-substituted isomers. Dehydrogenation of the reaction products and subsequent hydrolysis make it possible to obtain 5-or 6-aminomethylindoles. |
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