Abstract: Salvadoricine is an indole alkaloid isolated from the leaves of Salvadora persica Linn. This natural product has interesting and diverse biological profile. An effective one-pot synthesis of Salvadoricine analogues via multicomponent reaction of α-amidoalkylation is proposed. The conditions for the reaction of benzothiazole, alkyl chloroformates and 3-acetylindole were found. The structure of the obtained in good yields analogues of natural alkaloid - Salvadoricine was proved by spectral methods.