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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228790Generated: October 25, 2026

Dimethylformamide → 4-[2-(3,5-Difluoro-phenyl)-6-methyl-pyridin-3-yloxy]-6,7-dimethoxy-quinoline

https://huagongshe.com/reaction/228790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant(3,5-Difluorophenyl)boronic acidHCID 2734338—
Reactant4-[(2-Iodo-6-methyl-3-pyridyl)oxy]-6,7-dimethoxyquinolineHCID 10093673—
SolventWaterHCID 962—
Product4-[2-(3,5-Difluoro-phenyl)-6-methyl-pyridin-3-yloxy]-6,7-dimethoxy-quinolineHCID 5775635347.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

N,N-Dimethylformamide (1 ml) and a 2 M aqueous potassium carbonate solution (1 ml) were added to 4-(2-iodo-6-methyl-pyridin-3-yloxy)-6,7-dimethoxy-quinoline (compound 116) (50 mg), tetrakistriphenylphosphine palladium (14 mg), and 3,5-difluorophenylboronic acid (56 mg) under an argon atmosphere, and the mixture was stirred at 70° C. for 5 hr. The reaction solution was cooled to room temperature, water was then added thereto, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using chloroform-methanol to give the title compound (23 mg, yield 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-17cf456e60b04877a3df7e0c1e32d90a
Source noteuspto-grants-2009_07