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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434592Generated: November 1, 2026

Triethylamine → 1-[1-(3-chloro-3-phenylpropyl)piperidin-4-yl]-5-(methylsulfonyl)-1H-benzimidazole

https://huagongshe.com/reaction/1434592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 68704632HCID 68704632—
SolventDichloromethaneHCID 6344—
Product1-[1-(3-chloro-3-phenylpropyl)piperidin-4-yl]-5-(methylsulfonyl)-1H-benzimidazoleHCID 57936011—

Reaction Steps

Methanesulphonyl chloride (0.46 ml) was added to a solution of 3-{4-[5-(methylsulfonyl)-1H-benzimidazol-1-yl]piperidin-1-yl}-1-phenylpropan-1-ol (2.1 g) and triethylamine (0.9 ml) in dichloromethane (30 ml) at 0° C. The mixture was allowed to warm to room temperature and stirring was continued for 16 hours. The reaction mixture was washed with water (15 ml) and brine (15 ml) and dried. Removal of the solvent gave the title compound as an orange foam, yield 1.85 g, M+H 432.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615555B2
Source datasetuspto-grants-2009_11
ORD IDord-bcbab8cc4ebf4c97bbb1eab318b4c20c
Source noteuspto-grants-2009_11