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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884091Generated: October 30, 2026

Thiazolidinedione → HCID 86616530, compound

https://huagongshe.com/reaction/884091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidine, acetateHCID 9793820—
ReactantHCID 86616531HCID 86616531—
SolventTolueneHCID 1140—
ProductHCID 86616530HCID 86616530—

Reaction Steps

To a solution of 3-methyl-4-(5-nitropyridin-2-yloxy)benzaldehyde (600 mg, 2.32 mmol) in toluene (35 mL) were added 2,4-thiazolidinedione (270 mg, 2.31 mmol) and piperidine acetate (135 mg, 0.93 mmol). The resulting solution was attached to a Dean Stark, and stirred under reflux for 1.5 hours. After being left to cool for 17 hours at room temperature, the precipitated yellow powder was filtered, to thereby yield 600 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236826B2
Source datasetuspto-grants-2012_08
ORD IDord-1bb1dc351693424d816c7fee097cfb5b
Source noteuspto-grants-2012_08