Lithium Hydroxide → 2-[4-(5-Chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]-3-methylbutanoic acid
反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:24]#[N:25])=[C:6]([C:8]2[CH:13]=[CH:12][N:11]([CH:14]([CH:20]([CH3:22])[CH3:21])[C:15]([O:17]CC)=[O:16])[C:10](=[O:23])[CH:9]=2)[CH:7]=1.[OH-].[Li+]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:24]#[N:25])=[C:6]([C:8]2[CH:13]=[CH:12][N:11]([CH:14]([CH:20]([CH3:22])[CH3:21])[C:15]([OH:17])=[O:16])[C:10](=[O:23])[CH:9]=2)[CH:7]=1参加物
3
実験手順
117 mg (purity 81%, 0.26 mmol) of ethyl 2-[4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]-3-methylbutanoate (racemate) were hydrolysed with lithium hydroxide according to General Method 6B. Yield: 79 mg (purity 86%, 78% of theory)
出典と根拠
- ORDレコード
- ord-f9053b2254e54c4296cae85413dedad1
- 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…