戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 625753作成日:2026年10月25日

Oxalyl chloride → 2-(2-Bromo-2-(4-fluorophenyl)acetamido)-4-fluorobenzamide

https://huagongshe.com/reaction/625753

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物2-Amino-4-fluorobenzamideHCID 10241004—
反応物Bromo(4-fluorophenyl)acetic acidHCID 16217752—
溶媒PyridineHCID 1049—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物2-(2-Bromo-2-(4-fluorophenyl)acetamido)-4-fluorobenzamideHCID 66610889—

反応条件

温度0 °C

反応手順

To a solution of 2-bromo-2-(4-fluorophenyl)acetic acid (425 mg, 1.82 mmol) in DCM (5 mL) and DMF (0.05 mL) was added oxalyl chloride (0.17 mL, 1.91 mmol) and the solution was stirred for 0.75 h. The solution was then cooled to 0° C. and a solution of 2-amino-4-fluorobenzamide (267 mg, 1.73 mmol) in pyridine (1 mL) was added. The solution was stirred at rt for 1 h and then evaporated. The crude residue was partitioned between EtOAc and 2 N HCl. The EtOAc layer was evaporated to give 2-(2-bromo-2-(4-fluorophenyl)acetamido)-4-fluorobenzamide as a crude oil which was used without further purification. (420 mg, 62%). LC-MS (ESI) m/z 369 (M−H)—.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09308207B2
出典データセットuspto-grants-2016_04
ORD IDord-6d6a742a0aa540a0a63b152078c2fb70
出典メモuspto-grants-2016_04