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HRID 486272作成日:2026年10月25日
Diethyl (ethoxymethylene)malonate → diethyl [N-cyclopropyl-N-[3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl]amino-methylene]malonate
https://huagongshe.com/reaction/486272
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| 反応物 | 3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitro-N-cyclopropylaniline | HCID 18974495 | — |
| 生成物 | diethyl [N-cyclopropyl-N-[3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl]amino-methylene]malonate | HCID 19418744 | — |
反応手順
To 3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitro-N-cyclopropylaniline (1.57 g) is added diethyl ethoxymethylenemalonate (1.45 ml) and the mixture is heated at 150° C. for 25 hours. After cooling, the reaction product is purified by silica-gel column-chromatography (dichloromethane : methanol=100:1) to give diethyl [N-cyclopropyl-N-[3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl]aminomethylene]malonate (1.50 g). The product is dissolved in acetic anhydride (7.9 ml) and thereto conc. sulfuric acid (3.16 ml) is added dropwise at 50°-60° C., followed by stirring for 30 minutes. The resultant mixture is poured into ice-water, neutralized, extracted with dichloromethane and the extract is dried The solvent is distilled off under reduced pressure. Purification by silica-gel column-chromatography (dichloromethane: methanol=10:1) to give ethyl 7-(1-piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylate (26 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05290934 |
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| 出典データセット | uspto-grants-1994_03 |
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| ORD ID | ord-950b467a75a04327b2e9a3a90f18be1a |
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| 出典メモ | uspto-grants-1994_03 |
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