2-Aminopropanol → 5-Bromo-2-(2-hydroxy-1-methylethyl)isoindolin-1-one
反応式
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O-:8])=O)=[C:4]([CH2:11]Br)[CH:3]=1.[NH2:13][CH:14]([CH3:17])[CH2:15][OH:16]>>[Br:1][C:2]1[CH:3]=[C:4]2[C:5](=[CH:9][CH:10]=1)[C:6](=[O:8])[N:13]([CH:14]([CH3:17])[CH2:15][OH:16])[CH2:11]2参加物
3
実験手順
This compound was prepared by using procedures analogous to those described for the synthesis of Example 52, Step 6 starting from 4-bromo-2-(bromomethyl)benzoate and 2-aminopropanol (Aldrich Cat No. 192171). LCMS (M+H)+=270.1.
後処理
- customThis compound was prepared
出典と根拠
- ORDレコード
- ord-96d4bab3cf9b4ceab24ecdb9257830b6
- 出典データセット
- uspto-grants-2016_02
- 特許番号
- US09266892B2
反応ノート
読み込み中…