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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 3-Cyclopropyl-3-Oxopropionic Acid Methyl Ester | HCID 10130016 | — |
| 反応物 | (2-Aminophenyl)(4-fluorophenyl)methanone methanesulfonate | HCID 53446970 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | Methyl 2-cyclopropyl-4-(4-fluorophenyl)quinoline-3-carboxylate | HCID 9901664 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06852862B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-f712a1cdd446458499e3e4380cc15777 |
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| 出典メモ | uspto-grants-2005_02 |
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