戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 928304作成日:2026年10月25日

2-Amino-4-fluoropyridine → N-(4-fluoropyridin-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

https://huagongshe.com/reaction/928304

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4-fluoropyridineHCID 18327808—
反応物4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoyl chlorideHCID 57981666—
溶媒AcetonitrileHCID 6342—
生成物N-(4-fluoropyridin-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamideHCID 7122268894%

反応手順

To a solution of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoyl chloride (1.688 mmol, 450 mg) in acetonitrile (24.8 mL) was added 2-amino-4-fluoropyridine (4.22 mmol, 473 mg). The reaction mixture was stirred at room temperature for 1.5 h. The reaction mixture was concentrated to a small volume, 3% aq. citric acid solution (18 mL) was added and the mixture was extracted with dichloromethane (2×15 mL). The combined organic layer was washed with 3% aq. citric acid solution, dried over magnesium sulfate, filtered and evaporated to afford 542.2 mg of N-(4-fluoropyridin-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (94%) as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09290504B2
出典データセットuspto-grants-2016_03
ORD IDord-4cab51ebe3e24e50805575196fb308f6
出典メモuspto-grants-2016_03