Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357141Generated: October 26, 2026

Water → 3-[4-(Imidazo[1,2-a]pyridin-5-ylsulfonyl)butyl]thiazolidine-2,4-dione

https://huagongshe.com/reaction/357141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThiazolidinedioneHCID 5437—
Reactant1,8-Diazabicyclo[5.4.0]undec-2-eneHCID 9812821—
Reactant5-(4-Chlorobutylsulfonyl)imidazo[1,2-a]pyridineHCID 18936865—
SolventDimethylformamideHCID 6228—
Product3-[4-(Imidazo[1,2-a]pyridin-5-ylsulfonyl)butyl]thiazolidine-2,4-dioneHCID 18936763—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 0.27 g (1.0 mmol) of 5-(4-chlorobutylsulfonyl)imidazo[1,2-a]pyridine and 0.177 g (1.0 mmol) of thiazolidine-2,4-dione in 7 ml of N,N-dimethylformamide, 0.15 ml (1.0 mmol) of 1,8-diazabicyclo[5.4.0]-undecene was added, followed by heating at 80° C. for 16 hours. After cooling, the reaction mixture was poured into water, extracted with ethyl acetate, washed with water and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent, chloroform→chloroform/methanol=50/1) to yield 0.22 g (62.2%, light yellow oily substance) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840732
Source datasetuspto-grants-1998_11
ORD IDord-6bf2f688afb946ceb7d2131c8f22c8fa
Source noteuspto-grants-1998_11