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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357203Generated: October 26, 2026

Piperidine → 5-[3-(4-Methoxyphenyl)propylidene]-3-[4-(imidazo[1,2-a]pyridin-5-yl-thio)butyl]thiazolidine-2,4-dione

https://huagongshe.com/reaction/357203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3-(4-Methoxyphenyl)propanalHCID 11126607—
Reactant3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dioneHCID 18936694—
SolventEthanolHCID 702—
Product5-[3-(4-Methoxyphenyl)propylidene]-3-[4-(imidazo[1,2-a]pyridin-5-yl-thio)butyl]thiazolidine-2,4-dioneHCID 57298327—

Reaction Steps

To a solution of 964 mg (3.0 mmol) of 3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dione and 657 mg (4.0 mmol) of 3-(4-methoxyphenyl)-1-propanal in 20 ml of ethanol, 26 mg (0.3 mmol) of piperidine was added, followed by refluxing for 3.5 hours. After the reaction mixture was cooled, the solvent was distilled off. The residue was dissolved in dichloromethane, washed with purified water and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent, chloroform/methanol=50/1) to yield 1.08 g (76.8%, yellow oily substance) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840732
Source datasetuspto-grants-1998_11
ORD IDord-9cbe74fbbc414d498ee5f1234c71ecf3
Source noteuspto-grants-1998_11