Sodium Acetate → HCID 178441860、化合物
反応式
Br[CH2:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[NH:9][C:8]([CH2:13][CH2:14][CH2:15][CH3:16])=[N:7][C:6]2=[O:17].[C:18]([O-:21])(=[O:20])[CH3:19].[Na+]>CN(C=O)C>[C:18]([O:21][CH2:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[NH:9][C:8]([CH2:13][CH2:14][CH2:15][CH3:16])=[N:7][C:6]2=[O:17])(=[O:20])[CH3:19]参加物
4
反応条件
- 温度
- 60 °C
実験手順
To a solution of 2.1 g (7.0 mmol) of the quinazolinone prepared in Example 18 in 15 mL of dry DMF was added 1.74 g (20.0 mmol) of sodium acetate. The mixture was heated to 60° C. for 3 hours. The reaction mixture was concentrated in vacuo and the residue dissolved in 100 mL of CH2Cl2. The solution was washed with water (3×20 mL), brine (1×20 mL) and dried over MgSO4. The mixture was filtered and concentrated in vacuo. The residue was recrystallized from MeOH/H2O to give the titled compound as a colorless solid. 68% yield. 1H-NMR (CDCl3): 0.99 (t, 3H, J=7.32 Hz), 1.50 (m, 2H), 1.83 (m, 2H), 2.14 (t, 3H), 2.77 (3 line m, 2H, J=7.71 Hz), 5.23 (s, 2H), 7.69-7/78 (m, 2H), 8.25 (s, 1H), 10.90 (bs, 2H).
後処理
- concentrationThe reaction mixture was concentrated in vacuo
- dissolutionthe residue dissolved in 100 mL of CH2Cl2
- washThe solution was washed with water (3×20 mL), brine (1×20 mL)
- dry with materialdried over MgSO4
- filtrationThe mixture was filtered
- concentrationconcentrated in vacuo
- customThe residue was recrystallized from MeOH/H2O
出典と根拠
- ORDレコード
- ord-d5cc3aa040424c8486dd4c5f6f065f65
- 出典データセット
- uspto-grants-1993_08
- 特許番号
- US05238942
反応ノート
読み込み中…