反応式
C[O-].[Na+].CO[C:6](=[O:11])[C:7]([O:9][CH3:10])=[O:8].[C:12]([C:15]1[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=1)(=[O:14])[CH3:13]>CO>[O:11]=[C:6]([CH2:13][C:12](=[O:14])[C:15]1[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=1)[C:7]([O:9][CH3:10])=[O:8]参加物
実験手順
Sodium methoxide (5.4 g, 100 mmol) and dimethyloxalate (11.8 g, 100 mmol) were dissolved in anhydrous methanol (700 mL) and stirred at room temperature under nitrogen until a suspension was formed. To this mixture, 3-acetylpyridine (5.5 mL, 50 mmol) was added and the stirring was continued for 3 days at room temperature. The reaction was quenched with enough 5% aqueous KHSO4 until all solids have dissolved. The methanol was removed under reduced pressure, and the residue was extracted with ethyl acetate (3×200 mL). The combined organic layers were washed with water (2×200 mL), brine and dried (NaSO4) followed by the removal of solvent under reduced pressure to give the title compound (8.67 g, 84% yield) as a yellow solid. 1H NMR (CDCl3, 300 MHz) δ 9.21–9.20 (m, 1H), 8.84–8.82 (m, 1H), 8.30–8.26 (m, 1H), 7.50–7.45 (m, 1H), 7.08 (s, 1H), 3.96 (s, 3H). 13C NMR (CDCl3, 75 MHz) δ 188.5, 170.4, 162.2, 153.9, 149.0, 135.2, 130.5, 123.8, 98.0, 53.3. mass spectrum (APIMS) m/z 208 (M+1)+.
後処理
- customwas formed
- customThe reaction was quenched with enough 5% aqueous KHSO4 until all solids
- dissolutionhave dissolved
- customThe methanol was removed under reduced pressure
- extractionthe residue was extracted with ethyl acetate (3×200 mL)
- washThe combined organic layers were washed with water (2×200 mL), brine
- dry with materialdried (NaSO4)
- customfollowed by the removal of solvent under reduced pressure
出典と根拠
- ORDレコード
- ord-7a51bd60341c47f6bf110e2467dc0b37
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07087630B2
関連ノート
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