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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357822Generated: November 3, 2026

8-Hydroxyquinoline → HCID 24760450, compound

https://huagongshe.com/reaction/2357822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-HydroxyquinolineHCID 1923—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 18453089HCID 18453089—
ReactantHCID 178480364HCID 178480364—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 24760450HCID 2476045026.7%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of N-((1H-imidazol-4-yl)methyl)-4-chloro-1-methyl-1H-pyrrole-2-carboxamide (81 mg, 0.23 mmol), 1-(4-iodophenyl)pyridin-2(1H)-one (100 mg, 0.33 mmol), 8-hydroxyquinoline (15 mg, 0.10 mmol) and K2CO3 (193 mg, 1.40 mmol) in DMSO (2 mL) was degassed with Ar before being charged with CuI (21 mg, 0.11 mmol). The mixture in a sealed tube was heated at 130° C. overnight. It was then purified by HPLC to give the titled compound (25 mg). MS 408.1 and 410.1 (M+H, Cl pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763608B2
Source datasetuspto-grants-2010_07
ORD IDord-2639280e66a944e9ae37c14703d97620
Source noteuspto-grants-2010_07