Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608621Generated: October 27, 2026

Water → 5-[3-[3-(Phenyl)propyloxy]propylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1608621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant5-[3-(Hydroxy)propylthio]imidazo[1,2-a]pyridineHCID 23362890—
ReactantHCID 178418629HCID 178418629—
Product5-[3-[3-(Phenyl)propyloxy]propylthio]imidazo[1,2-a]pyridineHCID 2336284458.9%

Reaction Steps

To a solution of 5-[3-(hydroxy)propylthio]imidazo[1,2-a]pyridine (1.070 g, 5.137 mmoles) in tetrahydrofuran (30 ml) was added 60% sodium hydride in oil (0.25 g, 6.2 mmoles) with stirring under ice-cooling and the mixture was stirred under ice-cooling for 30 minutes. To the reaction mixture was added methyl iodie (1.53 g, 7.71 mmoles), followed by stirring at room temperature overnight. The reaction mixture was poured into water, which was extracted with methylene chloride (30 ml×3). The methylene chloride layers were combined and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethyl acetate) to obtain 0.987 g of the desired compound (58.9%, light brown oily product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-fe448be79e874b77aaa40da2e61709ba
Source noteuspto-grants-1995_03