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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081751Generated: October 27, 2026

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

https://huagongshe.com/reaction/1081751

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)ethylthioimidazo[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) under ice-cooling with stirring and the mixture was stirred under ice-cooling for 2 hours. The reaction mixture was washed in turn with aqueous saturated sodium bicarbonate 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 numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-cc3a9380f7e74d8ba98158dec605c3d1
Source noteuspto-grants-1996_12