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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1h-Benzimidazole,6-(chloromethyl)-1-[(2-chlorophenyl)methyl]-2-methyl-,hydrochloride | HCID 22620341 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Benzenesulfonylaminomethyl-1-(2-chlorobenzyl)-2-methylbenzimidazole | HCID 22620339 | 29.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06352985B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-5456d99127f94b09ae141e8d387c13ce |
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| Source note | uspto-grants-2002_03 |
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