戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 34038作成日:2026年10月25日

Triethylamine → 6-Fluoro-3-[(E)-2-(4-fluorophenyl)-vinyl]-5-nitro-1-trityl-1H-indazole

https://huagongshe.com/reaction/34038

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-FluorostyreneHCID 67883—
反応物2-(Di-tert-butylphosphino)biphenylHCID 2734215—
反応物3-bromo-6-fluoro-5-nitro-1-trityl-1H-indazoleHCID 68928300—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物6-Fluoro-3-[(E)-2-(4-fluorophenyl)-vinyl]-5-nitro-1-trityl-1H-indazoleHCID 6892849246.8%

反応条件

温度80 °C

反応手順

To a solution of 600 mg of 3-bromo-6-fluoro-5-nitro-1-trityl-1H-indazole in 6 mL of N,N-dimethylformamide were successively added 292 mg of 4-fluorostyrene, 71 mg of 2-(di-tert-butylphosphino)biphenyl, 27 mg of palladium acetate (II) and 0.85 mL of triethylamine, and stirred at 80° C. for 6.5 hours. The solvent was evaporated, and the resulting residue was dissolved in 25 mL of ethyl acetate. The organic layer was successively washed with water (twice) and saturated brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated. The obtained crude crystal was recrystallized from ethyl acetate-diisopropylether, to afford 304 mg of the title compound as bright yellow crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429609B2
出典データセットuspto-grants-2008_09
ORD IDord-3c4fee8c4bba47369bf067c0e1d01924
出典メモuspto-grants-2008_09