92406-42-3 → HCID 136404520, 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][CH2:16][CH2:17][O:18][C:19](=[O:34])[C:20](=[CH:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[N+:31]([O-:33])=[O:32])[C:21]([CH3:23])=O>>[CH3:14][O:15][CH2:16][CH2:17][O:18][C:19]([C:20]1[CH:24]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=2[N+:31]([O-:33])=[O:32])[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:21]=1[CH3:23])=[O:34]Participants
3
Procedure
Starting from 3-cyclohexyl-1-methyl-5-pyrazolamine and 2-methoxyethyl-2-(2-nitrobenzyliden)acetoacetate in about equimolar proportions.
Sources & evidence
- ORD record
- ord-ed620eb3424e49bfb492f89288ef58da
- Source dataset
- uspto-grants-1990_09
- Patent number
- US04954508
Reaction notes
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