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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5448Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/5448

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 an aqueous sodium bicarborate solution and water, dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethanol/ethyl 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 numberUS05244908
Source datasetuspto-grants-1993_09
ORD IDord-a1682d3d63114f3888105607aebf2126
Source noteuspto-grants-1993_09