Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081755Generated: October 26, 2026

Methyl chloroformate → 5-[2-(Methoxycarbonylamino)ethylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1081755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantTriethylamineHCID 8471—
Reactant5-[2-(Amino)ethylthio]imidazo[1,2-a]pyridineHCID 15229369—
SolventDichloromethaneHCID 6344—
Product5-[2-(Methoxycarbonylamino)ethylthio]imidazo[1,2-a]pyridineHCID 981641166.9%

Reaction Steps

To a solution of 5-[2-(amino)ethylthio]imidazo[1,2-a]pyridine (1.93 g, 10 mmoles) and triethylamine (1.53 ml, 11 mmoles) in methylene chloride (30 ml) was added methyl chloroformate (0.77 ml, 10 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 20 minutes. The reaction mixture was washed in turn with aqueous sodium bicarbonate and water and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography [eluent: ethanol/etyl acetate (1:10)] to obtain 1.68 g of the desired product (66.9%, colorless crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-b3fe52b2030344dc869ec66da096ec53
Source noteuspto-grants-1996_12