Electrophilic substitution reactions of indole alkaloids with α,β-unsaturated carbonyl compounds in the presence of K10 montmorillonite

Reactions of indole, 1-methylindole, and 3-methylindole with dimethyl acetylenedicarboxylate in the presence of K10 montmorillonite as a catalyst led to the formation of the corresponding dimethyl 2,2-bis(indolyl)butanedioates. The reaction of 2-methylindole with dimethyl acetylenedicarboxylate gave dimethyl 2-(2-methyl-1H-indol-3-yl)maleate and dimethyl 2-methyl-1H-1-benzoazepine-3,4-dicarboxylate. Dimethyl 1,5-dimethyl-1H-1-benzoazepine-3,4-dicarboxylate was obtained by treatment of 1,3-dimethylindole with dimethyl acetylenedicarboxylate using K10 clay as a catalyst. Published in Russian in Zhurnal Organicheskoi Khimii, 2006, Vol. 42, No. 6, pp. 900–902. The text was submitted by the authors in English.