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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081732Generated: November 1, 2026

Acetic Anhydride → 5-[3-(Acetyloxy)propylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1081732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant5-[3-(Hydroxy)propylthio]imidazo[1,2-a]pyridineHCID 23362890—
SolventDichloromethaneHCID 6344—
Product5-[3-(Acetyloxy)propylthio]imidazo[1,2-a]pyridineHCID 23362878100%

Reaction Steps

To a solution of 5-[3-(hydroxy)propylthio]imidazo[1,2-a]pyridine (2.00 g, 9.60 mmoles) and triethylamine (1.60 ml, 11.5 mmoles) in methylene chloride (50 ml) was added acetic anhydride (1.10 ml, 11.6 mmoles) with stirring at room temperature and the mixture was further stirred at room temperature for 7.5 hours. The reaction mixture was washed with an aqueous 1N sodium hydroxide solution and dried. After the solvent was distilled off, the residue was purified by column chromatography [eluent:hexane/acetone (1:1)] to obtain 2.40 g of the desired product (100%, brown oily product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-95f6e3dcb1594530aba8c34dc62e08fd
Source noteuspto-grants-1996_12