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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811446Generated: November 2, 2026

HCID 86613944, compound → HCID 86613946, compound

https://huagongshe.com/reaction/1811446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86613944HCID 86613944—
CatalystHCID 178418390HCID 178418390—
SolventDimethylformamideHCID 6228—
ProductHCID 86613946HCID 8661394688%

Reaction Steps

2.2 g of 10% palladium carbon was added to a DMF solution (20 ml) of 2.2 g of 5-(1-benzyl-8-hydroxy-2-oxo-1,2,3,4-tetrahydroquinolin-5-ylmethylidene)thiazolidine-2,4-dione, and the mixture was subjected to catalytic reduction at room temperature for 2 hours. The catalyst was removed by filtration, and the filtrate was concentrated. The residue was dissolved in ethyl acetate, washed with water and saturated sodium chloride solution, and concentrated. The residue was purified by silica gel column chromatography (dichloromethane:methanol=50:1). The purified product was recrystallized from a dichloromethane-ether mixed solvent, giving 1.9 g (88% yield) of 5-(1-benzyl-8-hydroxy-2-oxo-1,2,3,4-tetrahydroquinolin-5-ylmethyl)thiazolidine-2,4-dione as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362252B2
Source datasetuspto-grants-2013_01
ORD IDord-0d2a3e886f3c4b0b94ab56945bdcc1c5
Source noteuspto-grants-2013_01