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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499806Generated: October 31, 2026

8-Hydroxyquinoline → HCID 178474185, compound

https://huagongshe.com/reaction/499806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-HydroxyquinolineHCID 1923—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178474184HCID 178474184—
ReactantHCID 178523075HCID 178523075—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 178474185HCID 1784741856.6%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of (E)-N-(1-(4-iodophenyl)pyridin-2(1H)-ylidene)acetamide (120 mg, 0.27 mmol), 5-Chloro-N-((1H-imidazol-4-yl)methyl)thiophene-2-carboxamide 3-1 (109 mg, 0.30 mmol), 8-hydroxyquinoline (15 mg, 0.10 mmol) and K2CO3 (100 mg, 0.72 mmol) in DMSO (2 mL) was degassed with Ar before being charged with CuI (24 mg, 0.12 mmol). The mixture in a sealed tube was heated at 130° C. for 5 h. It was then purified by HPLC to give the titled compound (8 mg). MS 452.0 and 454.0 (M+H, Cl pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767697B2
Source datasetuspto-grants-2010_08
ORD IDord-faa28f3dd2ec4e46a51b47ded2e7b15d
Source noteuspto-grants-2010_08