戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 407237作成日:2026年10月24日

Potassium Fluoride → Methyl 4-amino-6-(4-chlorophenyl)-5-fluoro-3-methoxypicolinate

https://huagongshe.com/ja/reaction/407237

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium FluorideHCID 522689—
反応物2-(4-Chlorophenyl)-1,3,2-dioxaborinaneHCID 3468957—
反応物Trisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
反応物Methyl 4-amino-6-chloro-5-fluoro-3-methoxypicolinateHCID 86675409—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-amino-6-(4-chlorophenyl)-5-fluoro-3-methoxypicolinateHCID 7115069672.2%

反応条件

温度150 °C

反応手順

To a solution of methyl 4-amino-6-chloro-5-fluoro-3-methoxypicolinate (200 mg, 0.852 mmol) in CH3CN (1.246 mL) and H2O (1.246 mL) were added 2-(4-chlorophenyl)-1,3,2-dioxaborinane (251 mg, 1.279 mmol), KF (149 mg, 2.56 mmol), palladium(II) acetate (Pd(OAc)2; 19.14 mg, 0.085 mmol), and triphenylphosphine-3,3′,3″-trisulfonic acid trisodium salt (100 mg, 0.170 mmol). The reaction mixture was then heated in a bench top Biotage microwave at 150° C. for 5 min. The reaction mixture was diluted with CH2Cl2 and washed with H2O. The organic layer was separated, dried over MgSO4, filtered and concentrated. The crude residue was purified by normal phase chromatography (eluting with 10% EtOAc/40% CH2Cl2/50% hexanes) to afford the title compound as a tan solid (191 mg, 72.1%): mp 93-94° C.; 1H NMR (400 MHz, acetone-d6) δ 7.96 (dd, J=8.8, 1.4 Hz, 2H), 7.57-7.49 (m, 2H), 5.93 (s, 2H), 3.92 (s, 3H), 3.91 (s, 3H), ESIMS m/z 311 ([M+H]+), 309 ([M−H]−).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754229B2
出典データセットuspto-grants-2014_06
ORD IDord-9c18d074a7144da5a2d778269b02827d
出典メモuspto-grants-2014_06