HCID 10598128, compound → HCID 10621002, compound
Reaction equation
C([O:8][C:9]1[C:17]2[N:13]([C:14]([CH2:25][CH:26]3[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]3)=[C:15]([CH2:23][CH3:24])[C:16]=2[C:18](=[O:22])[C:19]([NH2:21])=[O:20])[CH:12]=[CH:11][CH:10]=1)C1C=CC=CC=1.CCCCCC.C[CH2:39][O:40][C:41]([CH3:43])=[O:42]>>[C:41]([CH2:43][O:8][C:9]1[C:17]2[N:13]([C:14]([CH2:25][CH:26]3[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]3)=[C:15]([CH2:23][CH3:24])[C:16]=2[C:18](=[O:22])[C:19]([NH2:21])=[O:20])[CH:12]=[CH:11][CH:10]=1)([O:40][CH3:39])=[O:42]Participants
3
Procedure
Mp, 149-150 C, (Hexane-EtOAc). 19% Yield from 49b.
Sources & evidence
- ORD record
- ord-1c0f5f9d7f91461a8b7ed224c06635f7
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06645976B1
Reaction notes
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