FIELD: organic chemistry. SUBSTANCE: compounds are synthesized by interaction of the corresponding aminoindole derivatives with carboxylic acid in the presence of an agent activating carboxylic acid in inert solvent. Carbonyldiimidazole is used as a preferable an acid-activating agent. 1,4-Dioxane diethyl ester or tetrahydrofuran is used as a solvent. Reaction is carried out at 0-65 C. Product: (R)-3-(N-benzylhydroxycarbonylpyrrolidine-2-yl-carbonyl)-5-di- benzylamino-1H-indole, m. p. is 176-177 C, |α|25 = +112 degree (in tetrahydrofuran, c = 1.0). Synthesized compounds can be used as pharmaceutical preparations for treatment of sicknesses caused by insufficient serotonin neurotransmission. EFFECT: improved method of synthesis. 7 cl, 1 tbl
Authors
Dates
1998-05-10—Published
1993-03-04—Filed