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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738189Generated: November 2, 2026

Thiazolidinedione → 5-{4-(3-Methylimidazo[5,4-b]pyridin-2-ylmethoxy)benzylidene}thiazolidine-2,4-dione

https://huagongshe.com/reaction/1738189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
ReactantBenzaldehyde,4-[(3-methyl-3h-imidazo[4,5-b]pyridin-2-yl)methoxy]-HCID 23298364—
SolventEthanolHCID 702—
Product5-{4-(3-Methylimidazo[5,4-b]pyridin-2-ylmethoxy)benzylidene}thiazolidine-2,4-dioneHCID 5436769379.2%

Reaction Steps

A mixture of 0.35 g of 2-(4-formylphenoxymethyl)-3-methylimidazo[5,4-b]pyridine (prepared as described in Preparation 112), 0.31 g of 2,4-thiazolidinedione, 0.26 ml of piperidine and 10 ml of ethanol was heated under reflux for 4 hours. At the end of this time, the solvent was removed by distillation under reduced pressure and the residue was crystallized by trituration with water. The crystals were collected by filtration and washed with water and then with ethyl acetate, to give 0.38 g of the title compound, melting at 279-281° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962470
Source datasetuspto-grants-1999_10
ORD IDord-3a3b108da50044c4b204292bae8d95d4
Source noteuspto-grants-1999_10