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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357083Generated: October 30, 2026

Butanal → 5-Butylidene-3-[4-(2-ethoxycarbonylimidazo[1,2-a]pyridin-8-yloxy)butyl]thiazolidine-2,4-dione

https://huagongshe.com/reaction/357083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanalHCID 261—
ReactantPiperidineHCID 8082—
Reactant3-[4-(2-Ethoxycarbonylimidazo[1,2-a]pyridin-8-yloxy)butyl]thiazolidine-2,4-dioneHCID 18936647—
SolventEthanolHCID 702—
Product5-Butylidene-3-[4-(2-ethoxycarbonylimidazo[1,2-a]pyridin-8-yloxy)butyl]thiazolidine-2,4-dioneHCID 57034303—

Reaction Steps

To a solution of 1.88 g (5.0 mmol) of 3-[4-(2-ethoxycarbonylimidazo[1,2-a]pyridin-8-yloxy)butyl]-thiazolidine-2,4-dione and 0.45 ml (5.0 mmol) of n-butyraldehyde in 20 ml of ethanol, 0.05 ml (0.5 mmol) of piperidine was added, followed by refluxing for 2 hours. After the reaction mixture was cooled, the solvent was distilled off. The residue was dissolved in chloroform, washed with saturated aqueous sodium hydrogen carbonate and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent, n-hexane/ethyl acetate=1/2) to yield 2.14 g (99.2%, yellow oily substance) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840732
Source datasetuspto-grants-1998_11
ORD IDord-1ad2eeea6dcf4dec8993aaa36b7e2bc3
Source noteuspto-grants-1998_11