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HRID 17525作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1,4-DioxaneHCID 31275—
反応物TrimethylboroxineHCID 574072—
反応物5-Amino-2-bromo-6-fluoro-4-methoxy-2-methylbiphenyl-3-carbonitrileHCID 68584833—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
生成物5-Amino-6-fluoro-4-methoxy-2-methylbiphenyl-3-carbonitrileHCID 86097509—

反応条件

温度110 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737166B2
出典データセットuspto-grants-2010_06
ORD IDord-41d3ba0b6a6148fcbd9992559d038a83
出典メモuspto-grants-2010_06