3-Nitrobenzaldehyde → HCID 135532341, compound
Reaction equation
[CH3:1][C:2]1([CH3:10])[CH2:7][CH2:6][C:5](=O)[CH2:4][C:3]1=[O:9].[N+:11]([C:14]1[CH:15]=[C:16]([CH:19]=[CH:20][CH:21]=1)[CH:17]=O)([O-:13])=[O:12].[NH2:22][C:23]1[CH:27]=[CH:26][NH:25][N:24]=1>>[CH3:1][C:2]1([CH3:10])[CH2:7][CH2:6][C:5]2[NH:22][C:23]3=[CH:27][CH:26]=[N:25][N:24]3[CH:17]([C:16]3[CH:19]=[CH:20][CH:21]=[C:14]([N+:11]([O-:13])=[O:12])[CH:15]=3)[C:4]=2[C:3]1=[O:9]Participants
4
Procedure
4,4-Dimethyl-1,3-cyclohexanedione, 3-nitrobenzaldehyde and 3-aminopyrazole were processed as described in General Procedure A to provide the title compound.
Sources & evidence
- ORD record
- ord-b3a009c4a9a146a6a397a7f06eba8194
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06538000B1
Reaction notes
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