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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081759Generated: October 25, 2026

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

https://huagongshe.com/reaction/1081759

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 5-(4-amino)butylthioimidazo[1,2-a]pyridine (370 mg, 1.67 mmoles) and triethylamine (0.35 ml, 2.51 mmoles) in methylene 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 aqueous saturated sodium bicarbonate and saturated saline, and then 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 numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-211dfeb751824b05ab69a08afa7c5a09
Source noteuspto-grants-1996_12