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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276062Generated: November 1, 2026

Water → 6-Benzenesulfonylaminomethyl-1-(2-chlorobenzyl)-2-methylbenzimidazole

https://huagongshe.com/reaction/276062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzenesulfonamideHCID 7370—
ReactantSodium hydrideHCID 24758—
Reactant1h-Benzimidazole,6-(chloromethyl)-1-[(2-chlorophenyl)methyl]-2-methyl-,hydrochlorideHCID 22620341—
SolventDimethylformamideHCID 6228—
Product6-Benzenesulfonylaminomethyl-1-(2-chlorobenzyl)-2-methylbenzimidazoleHCID 2262033929.7%

Reaction Steps

To a solution of 0.667 g of benzenesulfonic acid amide in 5 ml of N,N-dimethylformamide were added 0.127 g of 60% sodium hydride at room temperature, and the mixture was stirred for 1 hour. Further, 0.648 g of 1-(2-chlorobenzyl)-6-chloromethyl-2-methylbenzimidazole hydrochloride were added thereto, and the mixture was stirred at room temperature for 18 hours. Water was added to the reaction solution to stop the reaction, and the solvent was distilled off under reduced pressure. The residue was extracted with ethyl acetate and with water. The organic layer was concentrated, and was purified through silica-gel column chromatography (eluent: ethyl acetate) to give 0.240 g of 6-benzenesulfonylaminomethyl-1-(2-chlorobenzyl)-2-methyl-benzimidazole (264).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352985B1
Source datasetuspto-grants-2002_03
ORD IDord-5456d99127f94b09ae141e8d387c13ce
Source noteuspto-grants-2002_03