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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081729Generated: October 25, 2026

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

https://huagongshe.com/reaction/1081729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Naphthalenesulfonyl chlorideHCID 66560—
Reactant5-[4-(Amino)butylthio]imidazo[1,2-a]pyridineHCID 23362894—
SolventDichloromethaneHCID 6344—
Product5-[4-(1-Naphthalenesulfonylamino)butylthio]imidazo[1,2-a]pyridineHCID 2336288553.3%

Reaction Steps

To a solution of 5-[4-(amino)butylthio]imidazo[1,2-a]pyridine (300 mg, 1.36 mmoles) and triethylamine (0.29 ml, 2.08 mmoles) in methylene chloride (15 ml) was added 1-naphthalenesulfonyl chloride (307 mg, 1.35 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 1 hour. The reaction mixture was washed in turn with an aqueous sodium bicarbonate solution and water and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent:ethyl acetate) to obtain 296 mg of the desired product (53.0%, colorless solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-4e8fad51db3a491a830a50793fe9b7a2
Source noteuspto-grants-1996_12