Methyl 2-((3-nitrophenyl)methylene)-3-oxobutanoate → HCID 136404519, compound
Reaction equation
[CH:1]1([C:7]2[CH:11]=[C:10]([NH2:12])[N:9]([CH3:13])[N:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:14][O:15][C:16](=[O:31])[C:17](=[CH:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([N+:28]([O-:30])=[O:29])[CH:23]=1)[C:18]([CH3:20])=O>>[CH3:14][O:15][C:16]([C:17]1[CH:21]([C:22]2[CH:27]=[CH:26][CH:25]=[C:24]([N+:28]([O-:30])=[O:29])[CH:23]=2)[C:11]2[C:7]([CH:1]3[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]3)=[N:8][N:9]([CH3:13])[C:10]=2[NH:12][C:18]=1[CH3:20])=[O:31]Participants
3
Procedure
Starting from 3-cyclohexyl-1-methyl-5-pyrazolamine and methyl-2-(3-nitrobenzyliden)acetoacetate in equimolar proportions.
Sources & evidence
- ORD record
- ord-aaf35d178a044ec78e1b48b0f91d8554
- Source dataset
- uspto-grants-1990_09
- Patent number
- US04954508
Reaction notes
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