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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608612Generated: November 1, 2026

Triethylamine → 5-[4-(Methanesulfonamido)butylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1608612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant5-[4-(Amino)butylthio]imidazo[1,2-a]pyridineHCID 23362894—
SolventDichloromethaneHCID 6344—
Product5-[4-(Methanesulfonamido)butylthio]imidazo[1,2-a]pyridineHCID 2336286250.8%

Reaction Steps

To a solution of 5-[4-(amino)butylthio]imidazo[1,2-a]pyridine (440 mg, 1.99 mmoles) and triethylamine (0.42 ml, 3.01 mmoles) in methylene chloride (20 ml) was added methanesulfonyl chloride (0.19 ml, 2.45 mmoles) under ice-cooling with stirring and the mixture was stirred under ice-cooling for 1 hour. The reaction mixture was washed in turn with an aqueous saturated sodium bicarbonate solution and saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethyl acetate) to obtain 302 mg of the desired product (50.8%, light red brown solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-755b670acf204a89a5eb6ca5f3036de5
Source noteuspto-grants-1995_03