(S)-1-Benzyl-3-mesyloxypyrrolidine → (r)-6-(1-Benzylpyrrolidin-3-yloxy)-isoquinolin-1-ylamine
反応式
[CH2:1]([N:8]1[CH2:12][CH2:11][C@H:10]([O:13]S(C)(=O)=O)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:18][C:19]1[C:28]2[C:23](=[CH:24][C:25](O)=[CH:26][CH:27]=2)[CH:22]=[CH:21][N:20]=1>>[CH2:1]([N:8]1[CH2:12][CH2:11][C@@H:10]([O:13][C:25]2[CH:24]=[C:23]3[C:28](=[CH:27][CH:26]=2)[C:19]([NH2:18])=[N:20][CH:21]=[CH:22]3)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
3
実験手順
This compound was prepared from (S)-methanesulfonic acid 1-benzylpyrrolidin-3-yl ester and 1-amino-6-hydroxyisoquinoline by the procedure described in Example 1 to give the (R) 6-(1-benzylpyrrolidin-3-yloxy)-isoquinolin-1-ylamine product, El-MS: m/z=320.3 [M+H]+.
出典と根拠
- ORDレコード
- ord-460cd1046de4481ab224757e8ef6c692
- 出典データセット
- uspto-grants-2009_11
- 特許番号
- US07618985B2
反応ノート
読み込み中…