反応式
[C:1]([NH:4][C:5]1[CH:6]=[C:7](B(O)O)[CH:8]=[CH:9][CH:10]=1)(=[O:3])[CH3:2].[CH:14]([N:27]1[C:35]2[C:30](=[CH:31][C:32](Br)=[CH:33][CH:34]=2)[CH:29]=[C:28]1[C:37]([OH:39])=[O:38])([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[C:1]([NH:4][C:5]1[CH:6]=[C:7]([C:32]2[CH:31]=[C:30]3[C:35](=[CH:34][CH:33]=2)[N:27]([CH:14]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:28]([C:37]([OH:39])=[O:38])=[CH:29]3)[CH:8]=[CH:9][CH:10]=1)(=[O:3])[CH3:2]参加物
3
実験手順
The title compound was prepared according to the procedure described in Example 109 except that 3-acetamidobenzeneboronic acid and 1-benzhydryl-5-bromo-1H-indole-2-carboxylic acid were used.
出典と根拠
- ORDレコード
- ord-bc99c4b739364902ba9dabab16bfc870
- 出典データセット
- uspto-grants-2003_10
- 特許番号
- US06630496B1
関連ノート
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