Boc-L-Valine → HCID 22984573, compound
Reaction equation
C([NH:8][C@H:9]([C:13](O)=[O:14])[CH:10]([CH3:12])[CH3:11])(OC(C)(C)C)=O.[ClH:16].[NH2:17][N:18]1[C:24](=[O:25])[CH:23]([CH3:26])[C:22]2[CH:27]=[C:28]([F:31])[CH:29]=[CH:30][C:21]=2[C:20]2[CH:32]=[CH:33][CH:34]=[CH:35][C:19]1=2>>[ClH:16].[NH2:8][C@H:9]([C:13]([NH:17][N:18]1[C:24](=[O:25])[CH:23]([CH3:26])[C:22]2[CH:27]=[C:28]([F:31])[CH:29]=[CH:30][C:21]=2[C:20]2[CH:32]=[CH:33][CH:34]=[CH:35][C:19]1=2)=[O:14])[CH:10]([CH3:12])[CH3:11]Participants
3
Procedure
Following General Procedure D and using N-Boc-L-valine (Aldrich) and 5-amino-9-fluoro-7-methyl-5,7-dihydro-6H-dibenz[b,d]azepin6-one (Example 12), the title compound was prepared.
Sources & evidence
- ORD record
- ord-2fbaefe874db4bd7a43f57bd6eabb0ec
- Source dataset
- uspto-grants-2005_10
- Patent number
- US06958330B1
Reaction notes
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