Phenylalanine ethyl ester → HCID 68544400, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[N:9]([CH2:13][C:14]([OH:16])=O)[CH:8]=[CH:7]2)([O-:3])=[O:2].[CH2:17]([O:19][C:20](=[O:30])[C@H:21]([CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[NH2:22])[CH3:18]>>[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[N:9]([CH2:13][C:14]([NH:22][C@H:21]([C:20]([O:19][CH2:17][CH3:18])=[O:30])[CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:16])[CH:8]=[CH:7]2)([O-:3])=[O:2]Participants
3
Procedure
Ethyl N-[(5-nitro-1H-indol-1-yl)acetyl]-L-phenylalaninate was prepared from (5-nitro-1H-indol-1-yl)acetic acid and L-phenylalanine ethyl ester following the procedure of Example 10 Step 3: MS (ESI) m/z 396; MS (ESI) m/z 394.
Sources & evidence
- ORD record
- ord-1908c4eb46624998b3a6d7eb0f3e0ead
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07683091B2
Reaction notes
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