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HRID 731140作成日:2026年10月25日
5-fluoro-1,3-dihydro-2H-indol-2-one → 5-(5-Fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid
https://huagongshe.com/reaction/731140
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 5-fluoro-1,3-dihydro-2H-indol-2-one | HCID 3731012 | — |
| 反応物 | 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic Acid | HCID 11073792 | — |
| 触媒 | Piperidine | HCID 8082 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-(5-Fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid | HCID 53395102 | 101.4% |
反応手順
The reaction mixture of 5-fluorooxindole (100 mg, 0.66 mmol), 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (133 mg, 0.79 mmol), and 10 drops of piperidine in ethanol (3 mL) was stirred at 60° C. overnight and filtered. The solid washed with 1 M of aqueous hydrochloride solution, water, and dried to afford 5-(5-fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (201 mg, quantitative) as a yellow solid. MS m/z (relative intensity, %) 299 ([M−1]+., 100).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07582756B2 |
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| 出典データセット | uspto-grants-2009_09 |
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| ORD ID | ord-2789bc4114c74925a27d432d038a0eb3 |
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| 出典メモ | uspto-grants-2009_09 |
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