戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1480作成日:2026年10月24日

Triethylamine → 1-(5-Acetamido-2-chloro-4-fluorophenyl)-3-(2-propynyl)urea

https://huagongshe.com/ja/reaction/1480

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Phenyl chloroformateHCID 15891—
反応物PropargylamineHCID 239041—
反応物N-(5-amino-4-chloro-2-fluorophenyl)acetamideHCID 11769584—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物1-(5-Acetamido-2-chloro-4-fluorophenyl)-3-(2-propynyl)ureaHCID 53873711—

反応手順

A solution of 5'-amino-4'-chloro-2'-fluoroacetanilide (11.25 g, 55.6 mmol), and triethylamine (7.70 mL, 55.6 mmol) in tetrahydrofuran is added dropwise to a stirred solution of phenylchloroformate (8.70 mL, 69.4 mmol) in tetrahydrofuran while maintaining the reaction mixture temperature at 25°-30° C. After the addition is complete, the reaction mixture is stirred at room temperature for 75 minutes, and poured into ethyl acetate. The organic mixture is washed sequentially with water, saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a tan solid. A solution of the solid in tetrahydrofuran is treated with propargylamine (9.52 mL, 139 mmol), refluxed for 1 hour, and poured into water. The aqueous mixture is filtered to obtain a solid which is washed sequentially with water, 0.5N hydrochloric acid and water, and dried overnight to give the title product as a beige solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726126
出典データセットuspto-grants-1998_03
ORD IDord-5a556d937a384abda5eb0822445fcd79
出典メモuspto-grants-1998_03