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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5446Generated: October 28, 2026

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

https://huagongshe.com/reaction/5446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl IsocyanateHCID 12228—
Reactant5-[2-(Hydroxy)ethylthio]imidazo[1,2-a]pyridineHCID 14456849—
SolventDichloromethaneHCID 6344—
Product5-[2-(Methylcarbamoyloxy)ethylthio]imidazo[1,2-a]pyridineHCID 2336281785.2%

Reaction Steps

To a solution of 5-[2-(hydroxy)ethylthio]imidazo[1,2-a]pyridine (971 mg, 5 mmoles) and trietylamine (0.91 ml, 6.53 mmoles) in methylene chloride (40 ml) was added methyl isocyanate (0.65 ml, 11 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 12 hours. The reaction mixture was washed with saturated saline and dried over anhydrous magnesium sulfater. After the solvent was distilled off, the residue was purified by column chromatography (eluent: methanol/chloroform=1:20) to obtain 1.07 g of the desired product (85.2%, colorless crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244908
Source datasetuspto-grants-1993_09
ORD IDord-38cd054a169a4254b93577d431c563a5
Source noteuspto-grants-1993_09