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HRID 23772作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/23772

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 990166490.4%

反応条件

温度80 °C

反応手順

694.1 kg of methyl 3-cyclopropyl-3-oxopropionate and 1447.8 kg of 2-amino-4′-fluorobenzophenone methanesulfonate were added to 8455 kg of 2-propanol, and 2-propanol was distilled off at 79 to 87° C. After distilling off 7553 kg of 2-propanol, 66.1 kg 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 HPLC showed that the residual amount of 2-amino-4′-fluorobenzophenone as a raw material was 0.5%. 8455 kg of toluene was added into the reaction solution, and the reaction solution was washed with 4620 kg of 4% aqueous solution of sodium hydroxide, then 2010 kg of 2% aqueous solution of sodium hydroxide, and finally 1585 kg of 5% brine solution. The reaction solution was dried over 158 kg of anhydrous magnesium sulfate to obtain 10220 kg of a toluene solution containing 1350 kg of methyl 2-cyclopropyl-4-(4′-fluorophenyl)quinoline-3-carboxylate (converted yield: 90.4%). A part of the solution was concentrated, and the concentrated residue was recrystallized from toluene having the same mass as that of the residue and heptane having five times mass of the residue to obtain methyl 2-cyclopropyl-4-(4′-fluorophenyl)quinoline-3-carboxylate of HPLC purity 99.7%. The substance has the same properties as the substance of Example 1.

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-8ab886e98cda4b66ad7ec1443a3a68a0
出典メモuspto-grants-2005_02