戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 595797作成日:2026年10月25日

1,2-Dichloroethane → 4-(2,2-Difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acid

https://huagongshe.com/reaction/595797

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物Citric AcidHCID 311—
反応物DiisopropylethylamineHCID 81531—
反応物HOAtHCID 181649—
反応物4-Carboxy-3-fluorophenylboronic acidHCID 2763201—
反応物2,2-Difluoro-1-phenylethan-1-amineHCID 45282641—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物4-(2,2-Difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acidHCID 123534983—

反応手順

To a solution of 4-borono-2-fluorobenzoic acid (200 mg, 1.087 mmol), 2,2-difluoro-1-phenylethanamine (232 mg, 1.196 mmol), and DIEA (0.570 mL, 3.26 mmol) in THF (3.866 mL) and DMF (0.483 mL) was added HOAt (296 mg, 2.175 mmol) and EDC (521 mg, 2.72 mmol). After 3 h stirring at room temperature, 10% citric acid solution was added (pH ˜3) and extracted with 2-methyl THF and EtOAc (1:1). The organic layers were dried over anhydrous Na2SO4, filtered, and concentrated. The crude 4-(2,2-difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acid was obtained (90%) and used for the next step without purification. LCMS (m/z): 375.3 (MH+), 0.48 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242996B2
出典データセットuspto-grants-2016_01
ORD IDord-10da6daac0da476486f9959ec4a2ca54
出典メモuspto-grants-2016_01