Tandem Reduction, Ammonolysis, Condensation, and Deamination Reaction for Synthesis of Benzothiadiazines and 1-(Phenylsulfonyl)-1H-benzimidazoles

A novel route for a SnCl2-promoted tandem reduction, ammonolysis, condensation, and deamination reaction which uses nitrile and 2-nitro-N-phenylbenzenesulfonamide/N-(2-nitrophenyl)benzenesulfonamide to synthesize derivatives of benzothiadiazine/1-(phenylsulfonyl)-1H-benzimidazole has been developed. The method features convenient operation and good functional group tolerance. In addition, it employs unsensitive and inexpensive SnCl2/i-PrOH as the reaction reagent and provides a direct approach for the synthesis of pharmaceutically important targets.

Automated summary

A novel route for the synthesis of derivatives of benzothiadiazine/1-(phenylsulfonyl)-1H-benzimidazole has been developed, utilizing a SnCl2-promoted tandem reduction, ammonolysis, condensation, and deamination reaction. The method offers convenient operation, good functional group tolerance, and employs unsensitive and inexpensive SnCl2/i-PrOH as the reaction reagent, providing a direct approach for the synthesis of pharmaceutically important targets.