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HRID 20544作成日:2026年10月23日
Potassium Carbonate → 3-{2-chloro-4-[(dimethylamino)sulfonyl]phenoxy}-5-[(1S)-2-methoxy-1-methylethoxy]-N-(1-methyl-1H-pyrazol-3-yl)benzamide
https://huagongshe.com/ja/reaction/20544
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-chloro-4-fluoro-N,N-dimethylbenzenesulfonamide | HCID 697776 | — |
| 反応物 | 3-hydroxy-5-{[(2S)-1-methoxypropan-2-yl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)benzamide | HCID 59127178 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3-{2-chloro-4-[(dimethylamino)sulfonyl]phenoxy}-5-[(1S)-2-methoxy-1-methylethoxy]-N-(1-methyl-1H-pyrazol-3-yl)benzamide | HCID 11540937 | 688.3% |
反応手順
To a solution of 3-hydroxy-5-[(1S)-2-methoxy-(1-methylethyl)oxy]-N-(1-methyl-1H-pyrazol-3-yl)benzamide (152 mg, 0.50 mmol) in acetonitrile (3.5 mL) was added potassium carbonate (345 mg, 2.5 mmol) and 3-chloro-4-fluoro-N,N-dimethylbenzenesulfonamide (237 mg, 1.0 mmol) and the mixture was heated under microwave conditions at 160° C. for 2 hours. The mixtures were filtered and evaporated. The residue was purified by flash chromatography (eluting with an increasing gradient of 60 to 100% ethyl acetate in isohexane) to afford the title compound (1.8 g, 98%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07745475B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-083b80e7c49b4478bd4c79d11302e20a |
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| 出典メモ | uspto-grants-2010_06 |
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