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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29147Generated: October 25, 2026

Dimethylformamide → 1-(Methylsulfonyl)-1H-Benzimidazol-2-Amine

https://huagongshe.com/reaction/29147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-AminobenzimidazoleHCID 13624—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventDichloromethaneHCID 6344—
Product1-(Methylsulfonyl)-1H-Benzimidazol-2-AmineHCID 2299704528.7%

Reaction Steps

2-amino-benzimidazole (1.0 g, 7.5 mmol) was dissolved in 15 mL of anhydrous CH2Cl2 and 3 mL anhydrous DMF and cooled to ˜0° C. Trethylamine (1.6 mL, 1.5 eq.) was added followed by an addition of methanesulfonylchloride (580 μL, 7.5 mmol) over ˜1 minute. After 1 minute at ˜0° C., the reaction was warmed to RT. After 1 hour the reaction was quenched with water, and partitioned between a saturated sodium bicarbonate solution and CH2Cl2. The aqueous layer was extracted with CH2Cl2 and the combined organic layers were washed with water (2 times), brine then dried over NaSO4, filtered and the solvent was removed in vacuo to give 455 mg of N-methanesulfonyl-2-aminobenzimidazole. HPLC shows the material to be 91% pure, (ret. time=3.70). LCMS: obs. M+H@ 212.1 amu. The material was carried on without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419967B2
Source datasetuspto-grants-2008_09
ORD IDord-457a04e2ceaa47618209d9626c06d3bb
Source noteuspto-grants-2008_09