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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433395Generated: November 3, 2026

Potassium Carbonate → 6,7-Dimethoxy-4-(5-nitro-pyridin-2-yloxy)-quinoline

https://huagongshe.com/reaction/1433395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-nitropyridineHCID 78240—
Reactant6,7-Dimethoxy-4-hydroxyquinolineHCID 459611—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6,7-Dimethoxy-4-(5-nitro-pyridin-2-yloxy)-quinolineHCID 2293625134.1%

Reaction Steps

6,7-Dimethoxy-1,4-dihydro-4-quinolinone (4.10 g, 20.0 mmol), 2-bromo-5-nitropyridine (4.46 g, 22.0 mmol) and potassium carbonate (5.53 g, 40.0 mmol) were heated and stirred at 70° C. for 3 hours in N,N-dimethylformamide (20 ml). The reaction solution was diluted with ethyl acetate, the insoluble portion was filtered off, and after washing with water and saturated brine and drying the organic layer over anhydrous magnesium sulfate, the drying agent was filtered off and the filtrate was distilled off under reduced pressure. The obtained crude product was subjected to silica gel column chromatography (eluent: ethyl acetate), and the fraction containing the target substance was concentrated, suspended in ethyl acetate and diluted with hexane, after which the crystals were filtered out, washed with hexane and then blow-dried to obtain the title compound (2.23 g, 6.81 mmol, 34%) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612092B2
Source datasetuspto-grants-2009_11
ORD IDord-7253c81bca0e44ddabcd30ecbec61e6d
Source noteuspto-grants-2009_11