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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276908Generated: October 26, 2026

4-Nitrobenzenesulfonamide → 1-(2-Chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazole

https://huagongshe.com/reaction/1276908

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzenesulfonamideHCID 22784—
Reactant6-Carboxy-1-(2-Chlorobenzyl)-2-MethylbenzimidazoleHCID 18680817—
Reactant3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
SolventDimethylformamideHCID 6228—
Product1-(2-Chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazoleHCID 1868100346.5%

Reaction Steps

N,N'-carbodiimidazole (0.432 g) was added at a time to a solution of 0.400 g of 6-carboxy-1-(2-chlorobenzyl)-2-methylbenzimidazole in 15 ml of N,N-dimethylformamide, and the solution was stirred at room temperature for 1 hour. Subsequently, a solution of 0.538 g of 4-nitrobenzenesulfonamide and 0.405 g of diazabicycloundecene in 5 ml of N,N-dimethylformamide, and the mixture was stirred at 100° C. for 84 hours. The reaction solution was cooled, and the solvent was distilled off under reduced pressure. Chloroform and hydrochloric acid were added to the residue, and the mixture was stirred to precipitate the crystals. The crystals precipitated were separated through filtration, and were dried to give 0.300 g of 1-(2-chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazole (220).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166219
Source datasetuspto-grants-2000_12
ORD IDord-86bedd3ec8fe4d2b909a2f1c6b7011a6
Source noteuspto-grants-2000_12