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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559566Generated: October 30, 2026

8-Hydroxyquinoline → HCID 178474185, compound

https://huagongshe.com/reaction/559566

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 numberUS08063077B2
Source datasetuspto-grants-2011_11
ORD IDord-bdf89772379341ea98d7d66150557a7f
Source noteuspto-grants-2011_11