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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357211Generated: October 30, 2026

Piperidine → HCID 57112842, compound

https://huagongshe.com/reaction/357211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dioneHCID 18936694—
Reactant3-(2-Chlorophenyl)propanalHCID 21859726—
SolventEthanolHCID 702—
ProductHCID 57112842HCID 57112842—

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 738 mg (4.4 mmol) of 3-(2-chlorophenyl)-1-propanal in 20 ml of ethanol, 26 mg (0.3 mmol) of piperidine was added, followed by refluxing for 4.5 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 1.37 g (96.5%, yellow oily substance) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840732
Source datasetuspto-grants-1998_11
ORD IDord-476175562cd34e7997dbb50bbb073228
Source noteuspto-grants-1998_11