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Synthesis of 2-amino-3-(ω-aminoalkyl)indoles
Authors:A. N. Kost  V. G. Zabrodnyaya  Yu. N. Portnov  V. G. Voronin
Affiliation:(1) M. V. Lomonosov Moscow State University, USSR;(2) S. Ordzhonikidize Branch of the All-Union Scientific-Research Institute of Pharmaceutical Chemistry, Kupavna
Abstract:2-Amino-3-(ohgr-phthalimidoalkyl)indoles have been obtained by the rearrangement of ohgr-phthalimido acid beta-phenylhydrazides under the action of POCl3. The possibility has been studied of eliminating the phthalyl protective group from these compounds and a convenient method has been developed for obtaining 2-amino-3-(ohgr-aminoalkyl)indole dihydrochlorides. The behavior of the 2-amino-3-(ohgr-phthalimidoalkyl) indoles in alkylation reactions has been investigated.Deceased.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 484–488, April, 1980.
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