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HRID 476776作成日:2026年10月26日
Potassium tert-butoxide → Ethyl 8-chloro-1-cyclopropyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate
https://huagongshe.com/reaction/476776
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | HCID 178471875 | HCID 178471875 | — |
| 溶媒 | tert-Butanol | HCID 6386 | — |
| 生成物 | Ethyl 8-chloro-1-cyclopropyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 13579166 | — |
反応手順
To a solution of ethyl 2-(3-chloro-2,4,5-trifluorobenzoyl)-3-cyclopropylaminoacrylate in 40 ml of dry t-butanol is added a slurry of 1.20 g (10.7 mmol) of potassium t-butoxide in 20 ml of dry t-butanol. The reaction mixture is stirred at 6° C. for eight hours, then cooled to room temperature and concentrated. The residue is dissolved in chloroform, washed with water, dried over magnesium sulfate, filtered, and concentrated to give a pale brown solid. The crude product is purified by silica gel chromatography, and eluted with 80:20 chloroform:ethyl acetate to give 1.2 g of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04885386 |
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| 出典データセット | uspto-grants-1989_12 |
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| ORD ID | ord-9b6bc155da43466689375b0b4950888a |
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| 出典メモ | uspto-grants-1989_12 |
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