1-Methyl-3-(2-methylpropyl)-1H-pyrazol-5-amine → HCID 136404516, compound
Reaction equation
[CH3:1][N:2]1[C:6]([NH2:7])=[CH:5][C:4]([CH2:8][CH:9]([CH3:11])[CH3:10])=[N:3]1.[CH3:12][O:13][CH2:14][CH2:15][O:16][C:17](=[O:32])[C:18](=[CH:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=1[N+:29]([O-:31])=[O:30])[C:19]([CH3:21])=O>>[CH3:12][O:13][CH2:14][CH2:15][O:16][C:17]([C:18]1[CH:22]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[N+:29]([O-:31])=[O:30])[C:5]2[C:4]([CH2:8][CH:9]([CH3:11])[CH3:10])=[N:3][N:2]([CH3:1])[C:6]=2[NH:7][C:19]=1[CH3:21])=[O:32]Participants
3
Procedure
Starting from 1-methyl-3-(2-methylpropyl)-5-pyrazolamine and 2-methoxyethyl-2-(2-nitrobenzyliden)acetoacetate.
Sources & evidence
- ORD record
- ord-3306df132d5d4cf3b729f5f30855045e
- Source dataset
- uspto-grants-1990_09
- Patent number
- US04954508
Reaction notes
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