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HRID 1711981作成日:2026年10月26日
Perfluoro-1-butanesulfonyl fluoride → Perfluoro-1-butanesulfonic acid 7-methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl)-naphthalen-2-yl ester
https://huagongshe.com/reaction/1711981
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Perfluoro-1-butanesulfonyl fluoride | HCID 67814 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-ol | HCID 136352503 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Perfluoro-1-butanesulfonic acid 7-methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl)-naphthalen-2-yl ester | HCID 86602155 | 83.3% |
反応手順
A solution of 7-methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-ol (1.0 g, 2.4 mmol) in diisopropylethylamine (0.94 ml, 7.1 mmol) and dichloromethane (35 ml) was treated with N,N-dimethylaminopyridine (DMAP, 50 mg, 0.41 mmol) at 0° C. Then perfluoro-1-butanesulfonyl fluoride (0.51 ml, 2.8 mmol) was added dropwise and the resulting solution was stirred for 19 hrs at 23° C. The resulting solution was quenched with sat. aqueous ammonium chloride solution. The organic layer was separated and the water layer was extracted twice with dichloromethane. The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (hexane/EtOAc 3:1) to give 1.4 g (2.0 mmol) of the title compound as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07790882B2 |
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| 出典データセット | uspto-grants-2010_09 |
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| ORD ID | ord-7d724ff8c31f48fe9d5c48914b96e1c2 |
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| 出典メモ | uspto-grants-2010_09 |
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