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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382590Generated: November 2, 2026

Thiazolidinedione → HCID 74348953, compound

https://huagongshe.com/reaction/2382590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidinium acetateHCID 3014295—
ReactantHCID 86654536HCID 86654536—
SolventTolueneHCID 1140—
ProductHCID 74348953HCID 74348953—

Reaction Steps

To 4-benzooxazol-2-yl-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine-7-carbaldehyde [compound of Step VI] (0.176 g, 0.6 mmol) taken in toluene (25 mL) were added 2,4-thiazolidine dione (0.105 g, 0.9 mmol) and catalytic amount of piperidinium acetate (0.025 g). The resulting mixture was refluxed under Dean Stark conditions for 1.5 hours and then cooled in an ice-bath. The precipitate was filtered and washed with toluene and petroleum ether to give 5-(4-benzooxazol-2-yl-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepin-7-ylmethylene)-thiazolidine-2,4-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263587B2
Source datasetuspto-grants-2012_09
ORD IDord-878ac6f22dea4cf88896500d4a61f3b8
Source noteuspto-grants-2012_09