Glu asparagine → HCID 131724031, compound
Reaction equation
[NH2:1][C@H:2]([C:7]([NH:9][C@H:10]([C:15]([OH:17])=[O:16])[CH2:11][CH:12]([CH3:14])[CH3:13])=[O:8])[CH2:3][C:4](=[O:6])[NH2:5].[CH:18]([S:20]([CH:23]=[CH2:24])(=[O:22])=[O:21])=[CH2:19].[NH2:25][C@H:26]([C:32](O)=[O:33])[CH2:27][CH2:28][C:29](=[O:31])[OH:30].N[C@H](C(O)=O)CC(=O)N>>[NH2:25][C@H:26]([C:32]([NH:1][C@H:2]([C:7]([NH:9][C@H:10]([C:15]([OH:17])=[O:16])[CH2:11][CH:12]([CH3:14])[CH3:13])=[O:8])[CH2:3][C:4](=[O:6])[NH2:5])=[O:33])[CH2:27][CH2:28][C:29](=[O:30])[OH:31].[CH:18]([S:20]([CH:23]=[CH2:24])(=[O:22])=[O:21])=[CH2:19]Participants
3
Procedure
This compound is synthesized as described above for compound (i), except that Glu-asparagine is used in step (g).
Workup
- customThis compound is synthesized
Sources & evidence
- ORD record
- ord-fbf436705d0a4e2bb37f54ece2c73cf5
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06608030B1
Reaction notes
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