tert-Butyl bromoacetate → tert-Butyl (4-bromo-2-oxopyridin-1(2H)-yl)acetate
反応式
[Br:1][C:2]1[CH:7]=[CH:6][NH:5][C:4](=[O:8])[CH:3]=1.Br[CH2:10][C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12]>>[Br:1][C:2]1[CH:7]=[CH:6][N:5]([CH2:10][C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[C:4](=[O:8])[CH:3]=1参加物
3
実験手順
4.9 g (28.4 mmol) of 4-bromopyridin-2(1H)-one and 1.2 eq. of tert-butyl 2-bromoacetate were reacted according to General Method 4B at 120° C. After aqueous work-up, the crude product was reacted further without further purification. Yield: 8.6 g (purity 91%, 95% of theory)
後処理
- customaccording to General Method 4B at 120° C
出典と根拠
- ORDレコード
- ord-0ebd5d658add447c96942101750407a7
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09434690B2
反応ノート
読み込み中…