참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyclopropylamine | HCID 69828 | — |
| 반응물 | Ethyl 2-(2,4-dichloro-5-fluorobenzoyl)-3-ethoxyacrylate | HCID 53427585 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Fluoroquinolonic acid | HCID 483180 | — |
반응 단계
To a solution of 4 (80 g) in methylene chloride (800 mL), cyclopropylamine (44.0 g) was added with cooling below 10° C. The mixture was stirred at room temperature for 1 h and evaporated to a dry mixture. To the dry mixture in dimethoxyethane (800 mL), a 60% sodium hydride-in-oil suspension (12.0 g) was added slowly with cooling and stirring. The mixture was heated at 80-85° C. for 3 h under nitrogen atmosphere. It was cooled and water (5 L) was added and the precipitate was filtered and washed with water and dried. The ester was suspended in tetrahydrofuran (800 mL). A solution of sodium hydroxide (20.0 g) in water (500 mL) was added and the mixture was refluxed for 2 h. It was cooled and acidified with acetic acid and the precipitate was filtered. The solid was washed with water and acetone. wt=19.0 g of (7). m.p.=235-240° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06699989B1 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-7b128a3d112f49cfae0b3517a46e1728 |
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| 출처 메모 | uspto-grants-2004_03 |
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