関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 1-Fluoro-4-(methylsulphonyl)benzene | HCID 67994 | — |
| 反応物 | 5-Hydroxy-2-methyl-benzofuran-7-carboxylic acid methyl ester | HCID 59560341 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 5-(4-Methanesulfonyl-phenoxy)-2-methyl-benzofuran-7-carboxylic acid methyl ester | HCID 59560323 | 92% |
反応手順
Cs2CO3 (2.36 g, 7.24 mmol) and 4-flurophenyl methyl sulfone (631 mg, 3.62 mmol) were added to a solution of 5-hydroxy-2-methyl-benzofuran-7-carboxylic acid methyl ester (4d) (746 mg, 3.62 mmol) in DMF (5 mL). The mixture was heated to 120° C. overnight and then cooled to RT. The mixture was then quenched with H2O (80 mL) and extracted with EtOAc 92×100 ml). The combined organic layers were dried over MgSO4 and concentrated. The residue was purified by flash column chromatograph eluting with 4% CH3OH/CH2Cl2 to afford brown color oil (1.2 g, 92%). 1H NMR (400 MHz, CDCl3) δ 8.02 (s, 2 H) 7.86-7.90 (m, 1 H) 7.58 (d, J=2.53 Hz, 1 H) 7.38 (d, J=2.53 Hz, 1 H) 7.05 (d, J=8.84 Hz, 1 H) 6.44 (s, 1H) 3.99 (s, 3 H) 3.05 (s, 3 H) 2.56 (s, 3 H); LCMS for C18H16O6S m/z 361.00 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08119624B2 |
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| 出典データセット | uspto-grants-2012_02 |
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| ORD ID | ord-15e71aa9e627400ea65488bd1924fd73 |
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| 出典メモ | uspto-grants-2012_02 |
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