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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608613Generated: October 26, 2026

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

https://huagongshe.com/reaction/1608613

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 numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-b788c7702abc40b99ba25c643344b223
Source noteuspto-grants-1995_03