Indole-5-carboxaldehyde → HCID 86612423, compound
Reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([CH:10]=[O:11])=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[C:12]([O:16][C:17]([N:19]1[C:24]([CH3:26])([CH3:25])[CH2:23][CH2:22]OS1(=O)=O)=[O:18])([CH3:15])([CH3:14])[CH3:13]>>[C:12]([O:16][C:17]([NH:19][C:24]([CH3:25])([CH3:26])[CH2:23][CH2:22][N:1]1[C:9]2[C:4](=[CH:5][C:6]([CH:10]=[O:11])=[CH:7][CH:8]=2)[CH:3]=[CH:2]1)=[O:18])([CH3:15])([CH3:14])[CH3:13]Participants
3
Procedure
Prepared analogously to Component V(a) by alkylation of indole-5-carbaldehyde with N-tert-butoxycarbonyl-4,4-dimethyl-[1,2,3]oxathiazinane-2,2-dioxide (Component XI).
Sources & evidence
- ORD record
- ord-ab776c10f0124b30a8f476f7559ad14c
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07754756B2
Reaction notes
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