(-)-N-Acetylphenylalanine → N-Ac-D-Phe-2-Nal-OMe
Reaction equation
[NH:1]([C:13]([CH3:15])=[O:14])[C@@H:2]([C:10](O)=[O:11])[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[NH2:16][C@H:17]([C:29]([O:31][CH3:32])=[O:30])[CH2:18][C:19]1[CH:28]=[C:27]2[C:22]([CH:23]=[CH:24][CH:25]=[CH:26]2)=[CH:21][CH:20]=1>>[NH:1]([C:13]([CH3:15])=[O:14])[C@@H:2]([C:10]([NH:16][C@H:17]([C:29]([O:31][CH3:32])=[O:30])[CH2:18][C:19]1[CH:28]=[C:27]2[C:22]([CH:23]=[CH:24][CH:25]=[CH:26]2)=[CH:21][CH:20]=1)=[O:11])[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1Participants
3
Procedure
N-Ac-D-Phe-2-Nal-OMe was prepared according a similar manner as described in example 2 using N-Ac-D-Phe-OH and H-2-Nal-OMe.
Sources & evidence
- ORD record
- ord-8d674b2705c34cd0bdc6e15811e6ec26
- Source dataset
- uspto-grants-2000_03
- Patent number
- US06034067
Reaction notes
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