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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081742Generated: October 25, 2026

Water → 5-[1-(2-Thienylcarbonyl)-4-piperidyloxy]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1081742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant5-Chloroimidazo[1,2-A]pyridineHCID 10953722—
Reactant(4-Hydroxypiperidin-1-yl)(thiophen-2-yl)methanoneHCID 23362856—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-[1-(2-Thienylcarbonyl)-4-piperidyloxy]imidazo[1,2-a]pyridineHCID 233629644.6%

Reaction Steps

To a suspension of 60% sodium hydride in oil (0.40 g, 10 mmoles) in dimethylformamide (30 ml) was added 1-(2-thienylcarbonyl)-4-hydroxypiperidine (2.11 g, 10 mmoles) with stirring under ice-cooling and the mixture was stirred at room temperature for 30 minutes. To this reaction mixture was added 5-chloroimidazo[1,2-a]pyridine (1.53 g, 10 mmoles) with stirring under ice-cooling, followed by stirring at room temperature for 7 hours. Water was added to the reaction mixture, which was extratced with ethyl acetate and dried. After the solvent was distilled off, the residue was purified with column chromatography [eluent:ethyl acetate/hexane (1:1)→ethyl acetate/hexane (2:1)→ethyl acetate/ethanol (50:1)] to obtain 0.15 g of the desired product (4.6%, pale yellow oily product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-a1c10cd6dc674f42964146e24d155097
Source noteuspto-grants-1996_12