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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382562Generated: October 31, 2026

Methanesulfonyl chloride → (E)-5-Methysulfonylamino-1-(2-pyridyl)-2-styryl-1H-benzimidazole

https://huagongshe.com/reaction/382562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(E)-5-Amino-1-(2-pyridyl)-2-styryl-1H-benzimidazoleHCID 22736667—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product(E)-5-Methysulfonylamino-1-(2-pyridyl)-2-styryl-1H-benzimidazoleHCID 6994328534.5%

Reaction Steps

To a stirred solution of (E)-5-amino-1-(2-pyridyl)-2-styryl-1H-benzimidazole (162 mg, 0.52 mmol) in dichloromethane (3 ml) and pyridine (1 ml) was added a solution of methanesulfonyl chloride (63 mg, 0.55 mmol) in dichloromethane (2 ml) dropwise. The reaction mixture was stirred for 2 h at room temperature and then partitioned between ethyl acetate (50 ml) and saturated aqueous sodium bicarbonate solution (50 ml). The organic phase was separated and the aqueous phase was extracted with ethyl acetate (50 ml). The combined extracts were washed with brine (50 ml), dried (sodium sulfate) and concentrated in vacuo to give brown oil. It was purified by column chromatography (silica gel, 20 g; n-hexane/ethyl acetate (5/1)). Recrystallization of the residue from ethyl acetate afforded 70 mg (34%) of the titled compound as off white solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310079B1
Source datasetuspto-grants-2001_10
ORD IDord-b3c755b7b7f14b1a95869829c9d54def
Source noteuspto-grants-2001_10