戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1756799作成日:2026年10月24日

Water → 3-ethoxycarbonyl-6,7-difluoro-2-[N-cyclopropyl-N-(beta-ethoxycarbonylethyl)amino]quinoline

https://huagongshe.com/ja/reaction/1756799

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium CarbonateHCID 10340—
反応物2-Chloro-3-ethoxycarbonyl-6,7-difluoroquinolineHCID 9795461—
反応物Ethyl 3-(cyclopropylamino)propanoateHCID 13456042—
溶媒Acetic AcidHCID 176—
溶媒TolueneHCID 1140—
生成物3-ethoxycarbonyl-6,7-difluoro-2-[N-cyclopropyl-N-(beta-ethoxycarbonylethyl)amino]quinolineHCID 1899458565.6%

反応条件

温度20 °C

反応手順

3 g of sodium carbonate are added to a solution of 3.48 g of 2-chloro-3-ethoxycarbonyl-6,7-difluoroquinoline, prepared as described in Application Example 1, and 3 g of N-cyclopropyl-N-(b-ethoxycarbonylethyl)amine in 10 cm3 of toluene. The suspension obtained is heated to reflux and then stirred for 15 hours at this temperature. The reaction mixture is then cooled to approximately 20° C. and 30 cm3 of water and 4.5 cm3 of acetic acid are thereafter added. After settling has taken place, the reaction mixture is separated and washed with twice 10 cm3 of water. The organic phase is concentrated to dryness under reduced pressure (20 kPa) at approximately 50° C. 3.3 g of crude 3-ethoxycarbonyl-6,7-difluoro-2-[N-cyclopropyl-N-(b-ethoxycarbonylethyl)amino]quinoline are obtained in the form of an oil, which is used without further purification for the subsequent step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05442070
出典データセットuspto-grants-1995_08
ORD IDord-b8ce853ca604497faaa22c81f0a662de
出典メモuspto-grants-1995_08