N-[1(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine → HCID 13773284, compound
Reaction equation
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[S:13][CH:12]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[NH:11][N:10]=2)=[CH:5][CH:4]=1.[CH2:21]([O:23][C:24]([C@@H:26]([NH:35][C@H:36]([C:38](O)=[O:39])[CH3:37])[CH2:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)=[O:25])[CH3:22]>>[CH2:21]([O:23][C:24]([C@@H:26]([NH:35][C@H:36]([C:38]([N:11]1[N:10]=[C:9]([C:6]2[CH:5]=[CH:4][C:3]([S:2][CH3:1])=[CH:8][CH:7]=2)[S:13][C@H:12]1[C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])=[O:39])[CH3:37])[CH2:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)=[O:25])[CH3:22]Participants
3
Procedure
Prepared from the product of step e) and N-(1-(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanine by similar processes to those of Example 1, steps b and c as a yellow oil.
Sources & evidence
- ORD record
- ord-7eed08ff14a64eb8bf369a40503a33e3
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04927822
Reaction notes
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