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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504036Generated: November 1, 2026

Thiazolidinedione → HCID 86613944, compound

https://huagongshe.com/reaction/504036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantHCID 86613945HCID 86613945—
CatalystAcetic AcidHCID 176—
CatalystPiperidineHCID 8082—
SolventTolueneHCID 1140—
ProductHCID 86613944HCID 8661394499.8%

Reaction Steps

2.0 g of 1-benzyl-8-hydroxy-2-oxo-1,2,3,4-tetrahydroquinoline-5-carboxaldehyde and 0.874 g of 2,4-thiazolidinedione were suspended in 20 ml of toluene. Ten drops of piperidine and ten drops of acetic acid were added, followed by heating and refluxing for 8 hours. The resultant was allowed to cool to precipitate a solid, and the precipitated solid was collected by filtration and dried, giving 2.7 g (92% yield) of 5-(1-benzyl-8-hydroxy-2-oxo-1,2,3,4-tetrahydroquinolin-5-ylmethylidene)thiazolidine-2,4-dione as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777038B2
Source datasetuspto-grants-2010_08
ORD IDord-f87c42607ffd40a2be0671ced152e0e4
Source noteuspto-grants-2010_08