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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17525Generated: October 24, 2026

Potassium Carbonate → 5-Amino-6-fluoro-4-methoxy-2-methylbiphenyl-3-carbonitrile

https://huagongshe.com/en/reaction/17525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
ReactantTrimethylboroxineHCID 574072—
Reactant5-Amino-2-bromo-6-fluoro-4-methoxy-2-methylbiphenyl-3-carbonitrileHCID 68584833—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product5-Amino-6-fluoro-4-methoxy-2-methylbiphenyl-3-carbonitrileHCID 86097509—

Reaction Conditions

Temperature110 °C

Reaction Steps

5-Amino-2-bromo-6-fluoro-4-methoxy-2-methylbiphenyl-3-carbonitrile (I-235) (2.02 g, 6.29 mmol), potassium carbonate (2.61 g, 18.87 mmol) and tetrakis(triphenylphosphine)palladium(0) (727 mg, 0.63 mmol) were dissolved in 10% water-containing 1,4-dioxane (50 ml), and at room temperature, trimethylboroxine (50 wt. % tetrahydrofuran solution, 1.90 ml, 7.55 mmol) was added. After stirring under nitrogen atmosphere at 110° C. for 8 hours and then cooling to room temperature, tetrakis(triphenylphosphine)palladium(0) (727 mg, 0.63 mmol) was added, followed by further stirring at 110° C. for 11 hours. After cooling to room temperature, the insoluble matter was separated by filtration, the filtrate was fractionated with ethyl acetate and saturated brine. The organic layer was separated, the aqueous layer was again extracted with ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737166B2
Source datasetuspto-grants-2010_06
ORD IDord-41d3ba0b6a6148fcbd9992559d038a83
Source noteuspto-grants-2010_06