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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357013Generated: October 30, 2026

Sodium Iodide → 3-[2-(Imidazo[1,2-a]pyridin-5-yl)ethyl]thiazolidine-2,4-dione

https://huagongshe.com/reaction/357013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantThionyl ChlorideHCID 24386—
Reactant2-(Imidazo[1,2-a]pyridin-5-yl)ethanolHCID 21265869—
Reactant2,4-Thiazolidinedione sodium saltHCID 86738727—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product3-[2-(Imidazo[1,2-a]pyridin-5-yl)ethyl]thiazolidine-2,4-dioneHCID 18936757—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 4.0 g (24.7 mmol) of 5-(2-hydroxyethyl)imidazo[1,2-a]pyridine in 30 ml of chloroform, 5 ml (68 mmol) of thionyl chloride was added. After refluxing for 2 hours, the solvent was distilled off. To a suspension of the residue and 8.36 g (60 mmol) of 2,4-thiazolidinedione sodium salt in 50 ml of N,N-dimethylformamide, 3.75 g (25 mmol) of sodium iodide was added, followed by stirring at 80° C. for 16 hours. After the reaction mixture was cooled, water was added. The reaction mixture was then extracted with ethyl acetate and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent: n-hexane/ethyl acetate=2/1→1/1→1/4) to yield 1.00 g (15.5%, light orange powder) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840732
Source datasetuspto-grants-1998_11
ORD IDord-8022d0eff17842dc9617562550dc138d
Source noteuspto-grants-1998_11