1-Benzhydrylamino-2-(indol-3-yl)-ethanephosphonous acid → 1-Amino-2-(indol-3-yl)-ethanephosphonous acid
反応式
C([NH:14][CH:15]([P:26]([OH:28])[OH:27])[CH2:16][C:17]1[C:25]2[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=2)[NH:19][CH:18]=1)(C1C=CC=CC=1)C1C=CC=CC=1.C(NC(P(O)O)C(C)C)(C1C=CC=CC=1)C1C=CC=CC=1>>[NH2:14][CH:15]([P:26]([OH:28])[OH:27])[CH2:16][C:17]1[C:25]2[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=2)[NH:19][CH:18]=1参加物
3
実験手順
The procedure described in Example 36B was repeated using DL-1-benzhydrylamino-2-(indol-3-yl)-ethanephosphonous acid instead of DL-1-benzhydrylamino-2-methylpropanephosphonous acid to give DL-1-amino-2-(indol-3-yl)-ethanephosphonous acid.
出典と根拠
- ORDレコード
- ord-c2931da47b30492890e7be1818744cc2
- 出典データセット
- uspto-grants-1979_04
- 特許番号
- US04147780
反応ノート
読み込み中…