Acetone → HCID 68815972、化合物
反応式
[CH:1]([N:4]1[CH2:10][CH2:9][CH2:8][N:7]([C:11]([CH:13]2[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]2)=[O:12])[CH2:6][CH2:5]1)([CH3:3])[CH3:2].[CH3:19][C:20]([CH3:22])=[O:21].[C:23](O[BH-](OC(=O)C)OC(=O)C)(=[O:25])C.[Na+].[CH2:37](Cl)Cl>>[CH:1]([N:4]1[CH2:10][CH2:9][CH2:8][N:7]([C:11]([CH:13]2[CH2:14][CH2:15][N:16]([C:23]([O:21][C:20]([CH3:37])([CH3:22])[CH3:19])=[O:25])[CH2:17][CH2:18]2)=[O:12])[CH2:6][CH2:5]1)([CH3:3])[CH3:2]参加物
5
実験手順
The product of D8, Step 2 (2.0 g) was dissolved in DCM (50 ml) and acetone (0.94 ml) added and the mixture stirred for 5 min. Sodium triacetoxyborohydride (2.7 g) was then added and the reaction stirred at rt for 1.5 h. The reaction mixture was then washed with saturated potassium carbonate solution (50 ml), sodium hydrogen carbonate solution (3×50 ml) and brine (50 ml). The organic layer was dried (MgSO4) and evaporated to give the subtitled compound as a white solid (1.50 g).
後処理
- stirringthe reaction stirred at rt for 1.5 h
- washThe reaction mixture was then washed with saturated potassium carbonate solution (50 ml), sodium hydrogen carbonate solution (3×50 ml) and brine (50 ml)
- dry with materialThe organic layer was dried (MgSO4)
- customevaporated
出典と根拠
- ORDレコード
- ord-4355d4a6639e41e09905cb4ab546c64d
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07592347B2
反応ノート
読み込み中…