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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010130Generated: October 30, 2026

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

https://huagongshe.com/reaction/1010130

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 numberUS07973160B2
Source datasetuspto-grants-2011_07
ORD IDord-55fc2d8304bd49a2a05dca51f568e717
Source noteuspto-grants-2011_07