戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 483178作成日:2026年10月26日

Ethyl 4-chlorobenzoate → 2-(4-Chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid

https://huagongshe.com/reaction/483178

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4-chlorobenzoateHCID 81785—
反応物Sodium ethoxideHCID 2723922—
反応物2-Amino-3-(2-quinolon-3-yl)propionic acidHCID 13342097—
溶媒EthanolHCID 702—
生成物2-(4-Chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acidHCID 133421039%

反応手順

In 100 ml of ethanol, 1.66 g of ethyl p-chlorobenzate, 0.5 g of sodium ethylate and 2.09 g of 2-amino-3-(2-quinolon-3-yl)propionic acid were added and the whole mixture was placed in an autoclave. The reaction was carried out under 110 atmospheric pressure at 140°-150° C. for 6 hours. After completion of the reaction, the reaction mixture was cooled and concentrated under a reduced pressure. The residue was dissolved in 200 ml of chloroform, washed with 1%-potassium carbonate aqueous solution, a diluted hydrochloric acid and water in this order, then the chloroform layer was dried with sodium sulfate. The solvent was removed by distillation, the residue was recrystallized from ethanol-water to obtain 300 mg of 2-(4-chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid in the form of white powdery product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04578381
出典データセットuspto-grants-1986_03
ORD IDord-aa6fb9ed376f4ebcb8a81c60ad956e85
出典メモuspto-grants-1986_03