HCID 178472697, compound → HCID 178491120, compound
Reaction equation
C([O:3][C:4](=[O:36])[CH2:5][N:6]([CH2:27][C:28]1[CH:33]=[CH:32][C:31]([O:34][CH3:35])=[CH:30][CH:29]=1)[C:7](=[O:26])[C@H:8]([CH2:20][C:21]1[N:25]=[CH:24][NH:23][CH:22]=1)[NH:9][C:10]([O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:11])C.COC(=O)CN(C(=O)[C@H](CC1N=CNC=1)NC(OCC1C=CC=CC=1)=O)CC1C=CC(OCC2C=CC=CC=2)=CC=1>>[CH3:35][O:34][C:31]1[CH:32]=[CH:33][C:28]([CH2:27][N:6]([C:7](=[O:26])[C@H:8]([CH2:20][C:21]2[N:25]=[CH:24][NH:23][CH:22]=2)[NH:9][C:10]([O:12][CH2:13][C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)=[O:11])[CH2:5][C:4]([OH:36])=[O:3])=[CH:29][CH:30]=1Participants
3
Procedure
According to Example 1, Step 3, but substituting the compound from Step 2 above for N-[N-[(phenylmethoxy)carbonyl]-L-histidyl]-N-[[4-(phenylmethoxy)phenyl]methyl]glycine methyl ester, the title compound was obtained as a white solid.
Sources & evidence
- ORD record
- ord-ec1631f9672d49e08656baafad3e89b6
- Source dataset
- uspto-grants-1996_11
- Patent number
- US05571792
Reaction notes
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