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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608610Generated: October 26, 2026

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

https://huagongshe.com/reaction/1608610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-[2-(Amino)ethylthio]imidazo[1,2-a]pyridineHCID 15229369—
Reactant2-Acetylsalicyloyl chlorideHCID 57361564—
SolventDichloromethaneHCID 6344—
Product5-[2-[2-(Hydroxy)benzoylamino]ethylthio]imidazo[1,2-a]pyridineHCID 2336297756%

Reaction Steps

To a solution of 5-[2-(amino)ethylthio]imidazo[1,2-a]pyridine (3.87 g, 20 mmoles) and triethylamine (5.58 ml, mmoles) in methylene chloride (200 ml) was added o-acetylsalicyloyl chloride (4.77 g, 24 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. After the solvent was distilled off, ethanol (60 ml) and 1N NaOH (40 ml) were added to the residue, followed by strirring for 1 hour. 1N HCl (40 ml) was added and ethanol was distilled off, and then the residue was extracted with chloroform and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethyl acetate/ethanol=10:1) to obtain 3.51 g of the desired product (56.0%, colorless solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-eba409f04671494ab755179ec5ae31df
Source noteuspto-grants-1995_03