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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357843Generated: November 4, 2026

8-Hydroxyquinoline → HCID 24760603, compound

https://huagongshe.com/reaction/2357843

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-HydroxyquinolineHCID 1923—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 66974186HCID 66974186—
ReactantHCID 178523075HCID 178523075—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 24760603HCID 247606038.4%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 1-(4-iodo-3-(2-(piperidin-1-yl)ethoxy)phenyl)pyridin-2(1H)-one (116 mg, 0.22 mmol), N-((1H-imidazol-4-yl)methyl)-5-chlorothiophene-2-carboxamide 3-1 (85 mg, 0.24 mmol), 8-hydroxyquinoline (14 mg, 0.10 mmol) and K2CO3 (200 mg, 1.45 mmol) in DMSO (3 mL) was degassed with Ar before being charged with CuI (19 mg, 0.10 mmol). The mixture in a sealed tube was heated at 130° C. overnight. It was then purified by HPLC to give the titled compound (10 mg). MS 538.2 and 540.2 (M+H, Cl pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763608B2
Source datasetuspto-grants-2010_07
ORD IDord-dbfdda4d277d442696756baa6304a58a
Source noteuspto-grants-2010_07