Boc-L-Valine → HCID 23552797, 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]([CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[C:22]2[CH:32]=[CH:33][CH:34]=[CH:35][C:21]=2[C:20]2[CH:36]=[CH:37][CH:38]=[CH:39][C:19]1=2>>[ClH:16].[NH2:8][C@H:9]([C:13]([NH:17][N:18]1[C:24](=[O:25])[CH:23]([CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[C:22]2[CH:32]=[CH:33][CH:34]=[CH:35][C:21]=2[C:20]2[CH:36]=[CH:37][CH:38]=[CH:39][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-7-hexyl-5,7-dihydro-6H-dibenz[b,d]azepin-6-one (Example 11), the title compound was prepared.
Sources & evidence
- ORD record
- ord-ec27833797804774826343b445fd01e7
- Source dataset
- uspto-grants-2005_10
- Patent number
- US06958330B1
Reaction notes
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