Amantadine → N-Benzyloxycarbonyl-D-alanine 1-Adamantyl Amide
Reaction equation
[CH2:1]([O:8][C:9]([NH:11][C@@H:12]([C:14]([OH:16])=O)[CH3:13])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:17]12([NH2:27])[CH2:26][CH:21]3[CH2:22][CH:23]([CH2:25][CH:19]([CH2:20]3)[CH2:18]1)[CH2:24]2.C1CCC(N=C=NC2CCCCC2)CC1.C1C=CC2N(O)N=NC=2C=1>>[C:17]12([NH:27][C:14](=[O:16])[C@@H:12]([CH3:13])[NH:11][C:9]([O:8][CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)=[O:10])[CH2:24][CH:23]3[CH2:22][CH:21]([CH2:20][CH:19]([CH2:25]3)[CH2:18]1)[CH2:26]2Participants
4
Procedure
The title compound is prepared from N-benzyloxycarbonyl-D-alanine and 1-adamantanamine using the usual DCC-HOBt procedure described above.
Sources & evidence
- ORD record
- ord-a17dcf1f2cc24b90bd4e22482200e647
- Source dataset
- uspto-grants-1987_12
- Patent number
- US04714619
Reaction notes
Loading…