1-Benzhydrylamino-1-(fur-2-yl)-methanephosphonous acid → 1-Amino-1-(fur-2-yl)-methanephosphonous acid
Reaction equation
C([NH:14][CH:15]([C:19]1[O:20][CH:21]=[CH:22][CH:23]=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[O:20][CH:21]=[CH:22][CH:23]=1)[P:16]([OH:18])[OH:17]Participants
3
Procedure
The procedure described in Example 36B was repeated using DL-1-benzhydrylamino-1-(fur-2-yl)-methanephosphonous acid instead of DL-1-benzhydrylamino-2-methylpropanephosphonous acid to give DL-1-amino-1-(fur-2-yl)-methanephosphonous acid, melting point 221°.
Sources & evidence
- ORD record
- ord-d50c6d35cce0462a887d2be44f4c1621
- Source dataset
- uspto-grants-1979_04
- Patent number
- US04147780
Reaction notes
Loading…