戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2102186作成日:2026年10月25日

Cesium carbonate → 2-Cyclopropyl-1-({5-[2-fluoro-5-(trifluoromethyl)phenyl]-2-furanyl}methyl)-4-(trifluoromethyl)-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/2102186

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物3-Bromo-4-fluorobenzotrifluorideHCID 144295—
反応物Potassium AcetateHCID 517044—
反応物2-(4,5-Dimethyl-1,3,2-dioxaborolan-2-yl)-4,5-dimethyl-1,3,2-dioxaborolaneHCID 10198087—
反応物1-[(5-Bromo-2-furanyl)methyl]-2-cyclopropyl-4-(trifluoromethyl)-1H-indole-5-carbonitrileHCID 67404993—
触媒palladium(II) acetateHCID 167845—
触媒HCID 178418397HCID 178418397—
溶媒DimethylformamideHCID 6228—
生成物2-Cyclopropyl-1-({5-[2-fluoro-5-(trifluoromethyl)phenyl]-2-furanyl}methyl)-4-(trifluoromethyl)-1H-indole-5-carbonitrileHCID 866207161.7%

反応条件

温度90 °C

反応手順

To a solution of (1-[(5-bromo-2-furanyl)methyl]-2-cyclopropyl-4-(trifluoromethyl)-1H-indole-5-carbonitrile (Example 310C) (0.1 g, 0.24 mmol) in dry DMF (5 mL) was added potassium acetate (0.072 g, 0.73 mmol), palladium acetate (0.011 g, 0.048 mmol) and 4,4′,5,5′-tetramethyl-2,2′-bi-1,3,2-dioxaborolane (0.068 g, 0.264 mmol). The reaction is heated to 90° C. for 3 h. To the reaction was then added 2-bromo-1-fluoro-4-(trifluoromethyl)benzene (0.119 g, 0.48 mmol), cesium carbonate (0.159 g, 0.48 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.057 g, 0.048 mmol). The mixture was stirred at 85° C. overnight. Solids were filtered and the filtrate was then concentrated in vacuo. The residue was purified by radial chromatography (0-40% EtOAc-hexanes gradient) and by semipreparative HPLC to afford the title compound (0.002 g, 1.3% yield): MS (ES) m/z 493 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07572820B2
出典データセットuspto-grants-2009_08
ORD IDord-2fc2467b552f4a15a8d3615661a7f4c1
出典メモuspto-grants-2009_08