2-Nitrobenzaldehyde → HCID 178468900, compound
Reaction equation
[N+:1]([C:4]1[CH:11]=[CH:10][CH:9]=[CH:8][C:5]=1[CH:6]=O)([O-:3])=[O:2].[NH2:12][C:13]1[CH:17]=[CH:16][NH:15][N:14]=1.[C:18]([CH2:23][C:24]([O:26][CH2:27][CH3:28])=[O:25])(=O)[CH:19]([CH3:21])[CH3:20]>>[N+:1]([C:4]1[CH:11]=[CH:10][CH:9]=[CH:8][C:5]=1[CH:6]1[C:23]([C:24]([O:26][CH2:27][CH3:28])=[O:25])=[C:18]([CH:19]([CH3:21])[CH3:20])[NH:12][C:13]2=[N:14][NH:15][CH:16]=[C:17]12)([O-:3])=[O:2]Participants
4
Procedure
The title compound was prepared from 2-nitrobenzaldehyde, 3-aminopyrazole and ethyl isobutyrylacetate in the same manner as in Example 275.
Sources & evidence
- ORD record
- ord-a9e584adde43481da2560b38ee331448
- Source dataset
- uspto-grants-2005_12
- Patent number
- US06977262B2
Reaction notes
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