1-Benzhydrylamino-1-(indol-3-yl)-methanephosphonous acid → 1-Amino-1-(indol-3-yl)-methanephosphonous acid
Reaction equation
C([NH:14][CH:15]([C:19]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[NH:21][CH:20]=1)[P:16]([OH:18])[OH:17])(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]([C:19]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[NH:21][CH:20]=1)[P:16]([OH:17])[OH:18]Participants
3
Procedure
The procedure described in Example 36B was repeated using DL-1-benzhydrylamino-1-(indol-3-yl)-methanephosphonous acid instead of DL-1-benzhydrylamino-2-methylpropanephosphonous acid to give DL-1-amino-1-(indol-3-yl)-methanephosphonous acid.
Sources & evidence
- ORD record
- ord-9afa823ff91044e38b9668007ccaeb71
- Source dataset
- uspto-grants-1979_04
- Patent number
- US04147780
Reaction notes
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