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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081739Generated: October 27, 2026

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

https://huagongshe.com/reaction/1081739

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 moles) 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 numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-04761f3c1d6144c9bcaba5183d251d1c
Source noteuspto-grants-1996_12