3-(4-Hydroxypiperidin-1-yl)propanenitrile → 3-[2-(4-hydroxypiperidin-1-yl)ethyl]-2H-isoquinolin-1-one
反応式
C([N:3]([CH2:14][CH3:15])[C:4](=[O:13])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7](C)[C:6]=1[CH3:12])C.[OH:16][CH:17]1[CH2:22][CH2:21][N:20]([CH2:23]CC#N)[CH2:19][CH2:18]1>>[OH:16][CH:17]1[CH2:22][CH2:21][N:20]([CH2:23][CH2:15][C:14]2[NH:3][C:4](=[O:13])[C:5]3[C:6]([CH:12]=2)=[CH:7][CH:8]=[CH:9][CH:10]=3)[CH2:19][CH2:18]1参加物
3
実験手順
By the reaction in the same manner as in Example 1a, using N,N-diethyl-2,3-dimethylbenzamide (5.6017 g) and 3-(4-hydroxypiperidin-1-yl)propionitrile (2.26 g), 3-[2-(4-hydroxypiperidin-1-yl)ethyl]-2H-isoquinolin-1-one (327.5 mg) was obtained.
後処理
- customBy the reaction in the same manner as in Example 1a
出典と根拠
- ORDレコード
- ord-3294e3aa69ca4df7a87338fc3b6250d7
- 出典データセット
- uspto-grants-2010_10
- 特許番号
- US07812178B2
反応ノート
読み込み中…