Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5443Generated: October 26, 2026

Water → 5-[2-(Acetylamino)ethylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/5443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant5-[2-(Amino)ethylthio]imidazo[1,2-a]pyridine dihydrochlorideHCID 23362833—
SolventDimethylformamideHCID 6228—
Product5-[2-(Acetylamino)ethylthio]imidazo[1,2-a]pyridineHCID 2336288266.8%

Reaction Steps

To a solution of 5-[2-(amino)ethylthio]imidazo[1,2-a]pyridine dihydrochloride (2.66 g, 10 mmoles) and triethylamine (4.32 ml, 31 mmoles) in N,N-dimethylformamide (24 ml) was added acetyl chloride (0.71 ml, 10 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 4 hours. The reaction mixture was poured into water and extracted with chloroform. The chloroform layer was washed with saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:3) to obtain 1.57 g of the desired product (66.8%, colorless crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244908
Source datasetuspto-grants-1993_09
ORD IDord-c70f3f1b3dc840cb9734132ec78a68c7
Source noteuspto-grants-1993_09