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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608614Generated: October 25, 2026

Isopropyl chloroformate → 5-[4-(Isopropyloxycarbonylamino)butylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1608614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl chloroformateHCID 7917—
ReactantTriethylamineHCID 8471—
Reactant5-[4-(Amino)butylthio]imidazo[1,2-a]pyridineHCID 23362894—
SolventDichloromethaneHCID 6344—
Product5-[4-(Isopropyloxycarbonylamino)butylthio]imidazo[1,2-a]pyridineHCID 2336300241.9%

Reaction Steps

To a solution of 5-[4-(amino)butylthio]imidazo[1,2-a]pyridine (370 mg, 1.67 mmoles) and triethylamine (0.35 ml, 2.51 mmoles) in metylene chloride (20 ml) was added isopropyl chloroformate (0.25 g, 2.04 mmoles) under ice-cooling with stirring and the mixture was stirred under ice-cooling for 1 hour. The reaction mixture was washed in turn with an aqueous sodium bicarbonate solution and saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethyl acetate) to obtain 215 mg of the desired product (41.8%, light tan oily product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-58772ec7832a4ddd9fe0d8fcff664b9b
Source noteuspto-grants-1995_03