戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 23771作成日:2026年10月25日

3-Cyclopropyl-3-Oxopropionic Acid Methyl Ester → Methyl 2-cyclopropyl-4-(4-fluorophenyl)quinoline-3-carboxylate

https://huagongshe.com/reaction/23771

反応式

関与物質

役割名称HCID仕込み量
反応物3-Cyclopropyl-3-Oxopropionic Acid Methyl EsterHCID 10130016—
反応物(2-Aminophenyl)(4-fluorophenyl)methanone methanesulfonateHCID 53446970—
溶媒IsopropanolHCID 3776—
生成物Methyl 2-cyclopropyl-4-(4-fluorophenyl)quinoline-3-carboxylateHCID 990166489%

反応条件

温度80 °C

反応手順

12 g of methyl 3-cyclopropyl-3-oxopropionate and 25 g of 2-amino-4′-fluorobenzophenone methanesulfonate were added to 146 g of 2-propanol, and 2-propanol was distilled off at 79 to 83° C. After distilling off 119 g of 2-propanol over 6 hours, 1.14 g of methyl 3-cyclopropyl-3-oxopropionate was added and the mixture was heated at 79 to 81° C. for 4 hours. An analysis of the mixture with high performance liquid chromatography (HPLC) showed that the residual amount of 2-amino-4′-fluorobenzophenone as a raw material was 0.9%. 146 g of toluene was added into the reaction solution, and the reaction solution was washed with 80 g of 4% aqueous solution of sodium hydroxide and then 35 g of 2% aqueous solution of sodium hydroxide. The reaction solution was further washed with 25 g of 5% brine solution, and then dried over 5 g of anhydrous magnesium sulfate. Toluene was removed under a reduced pressure, and crystallization was carried out in 180 g of cyclohexane to obtain 22.9 g of methyl 2-cyclopropyl-4-(4′-fluorophenyl)quinoline-3-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852862B2
出典データセットuspto-grants-2005_02
ORD IDord-f712a1cdd446458499e3e4380cc15777
出典メモuspto-grants-2005_02