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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608588Generated: October 30, 2026

Triethylamine → 5-[2-(Methylsulfonyloxy)ethylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1608588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant5-[2-(Hydroxy)ethylthio]imidazo[1,2-a]pyridineHCID 14456849—
SolventDichloromethaneHCID 6344—
Product5-[2-(Methylsulfonyloxy)ethylthio]imidazo[1,2-a]pyridineHCID 2336296099.9%

Reaction Steps

To a solution of 5-[2-(hydroxy)ethylthio]imidazo[1,2-a]pyridine (9.71 g, 50 mmoles) and triethylamine (10.5 ml, 75.3 mmoles) in methylene chloride (300 ml) was added methanesulfonyl chloride (4.26 ml, 55 mmoles) with stirring under ice-cooling and the mixture was stirred under ice-cooling for 2 hours. The reaction solution was washed in turn with an aqueous saturated sodium bicarbonate solution and saturated saline and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off to obtain 13.6 g of the desired product (quantitative, brown oily product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-3ab2c88f87854e6383ce3cbe3a4e77b5
Source noteuspto-grants-1995_03