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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477140Generated: November 2, 2026

1,2-Dimethoxyethane → HCID 66917053, compound

https://huagongshe.com/reaction/1477140

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
ReactantFuran-2-boronic acidHCID 2734357—
ReactantHCID 66917247HCID 66917247—
CatalystHCID 178418807HCID 178418807—
SolventDichloromethaneHCID 6344—
ProductHCID 66917053HCID 6691705370%

Reaction Conditions

Temperature180 °C

Reaction Steps

8-bromo-5-fluoro-3-(4-methoxyphenyl)-1H-quinolin-4-one (150 mg, 0.43 mmol), 2-furan boronic acid (145 mg, 1.3 mmol), 1,1′-bis(diphenylphosphino)ferrocene dichloro palladium (II)-dichloromethane complex (PdCl2(DPPF)) (35 mg, 0.04 mmol) and a 2N sodium carbonate aqueous solution (1 ml) were added to 1,2-dimethoxyethane (3 ml), and the mixture was heated at 180° C. for 10 minutes (microwave reactor). After the reaction mixture was cooled to room temperature, dichloromethane was added, and then filtration with Celite was carried out. The filtrate was extracted with dichloromethane and washed with water. The organic layer was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was then purified by silica gel column chromatography (dichloromethane). The purified product was concentrated under reduced pressure, and the residue was recrystallized from n-hexane-ethyl acetate to thereby obtain 100 mg of powdery slightly orange 5-fluoro-8-furan-2-yl-3-(4-methoxyphenyl)-1H-quinolin-4-one (yield: 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403773B2
Source datasetuspto-grants-2016_08
ORD IDord-6f9086e2a6aa4a1b907c45782355f063
Source noteuspto-grants-2016_08