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HRID 130644作成日:2026年10月26日

Dimethylformamide → 3',4'-difluoro-N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)biphenyl-4-carboxamide

https://huagongshe.com/reaction/130644

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium CarbonateHCID 10340—
反応物3,4-Difluorobenzeneboronic acidHCID 2734337—
反応物N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)-4-iodobenzamideHCID 59731034—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
生成物3',4'-difluoro-N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)biphenyl-4-carboxamideHCID 5973103854.7%

反応条件

温度80 °C

反応手順

Next, to a solution of N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)-4-iodobenzamide (100 mg, 0.25 mmol) in a 3 to 1 mixture of DMF and H2O was added 3,4-difluorophenylboronic acid (80.3 mg, 0.51 mmol), tetrakis(triphenylphosphine)palladium(0) (8.82 mg, 0.01 mmol), and sodium carbonate (80.9 mg, 0.76 mmol). The mixture was stirred at 80° C. for 2.5 hours, and after cooled to room temperature, the product was extracted with diethyl ether. The organic layer was washed with water then brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. After triturated with ethylacetate and hexane, the solid was filtered to afford 3′,4′-difluoro-N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)biphenyl-4-carboxamide (51.9 mg, 54%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381840B2
出典データセットuspto-grants-2008_06
ORD IDord-a52936f01c8741b6a6197647ecdb7c82
出典メモuspto-grants-2008_06