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Trimethylsilyl iodide → 1-(4-(methylthio)phenyl)-4-(piperidin-4-yloxy)pyridin-2(1H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trimethylsilyl iodide | HCID 85247 | — |
| 反応物 | Benzyl 4-(1-(4-(methylthio)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate | HCID 67368480 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-(4-(methylthio)phenyl)-4-(piperidin-4-yloxy)pyridin-2(1H)-one | HCID 67368708 | 73.3% |
反応手順
To a stirring solution of benzyl 4-(1-(4-(methylthio)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate (367 mg, 0.815 mmol) in CH2Cl2 (5 mL) at 0° C. was added iodotrimethylsilane (0.33 mL, 2.4 mmol, Aldrich). The reaction was stirred for 40 min and then quenched at 0° C. with HCl (1N in H2O, 5 mL). To the resulting mixture was diluted with CH2Cl2 and extracted with H2O. The H2O layer was basified with NaOH (1N in H2O, 10 mL) and extracted with CH2Cl2 (2×). The combined organic layers were washed with brine, dried over Na2SO4 and concentrated in vacuo to yield 189 mg crude product as an off-white solid. MS (ESI) 317 (M+H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08232404B2 |
| 出典データセット | uspto-grants-2012_07 |
| ORD ID | ord-df8812161fcc461fa46a9d368fb065ce |
| 出典メモ | uspto-grants-2012_07 |