3-Amino-5-phenylpyrazole → HCID 178469195, compound
Reaction equation
[C:1]1([C:7]2[CH:11]=[C:10]([NH2:12])[NH:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:13]([O:15][C:16](=[O:30])[C:17](=[CH:21][C:22]1[CH:27]=[C:26]([CH3:28])[CH:25]=[CH:24][C:23]=1[CH3:29])[C:18]([CH3:20])=O)[CH3:14]>>[CH2:13]([O:15][C:16]([C:17]1[CH:21]([C:22]2[CH:27]=[C:26]([CH3:28])[CH:25]=[CH:24][C:23]=2[CH3:29])[C:11]2[C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)=[N:8][NH:9][C:10]=2[NH:12][C:18]=1[CH3:20])=[O:30])[CH3:14]Participants
3
Procedure
Starting from 3-phenyl-5-(1H)pyrazolamine and ethyl-2-(2,5-dimethylbenzyliden)acetoacetate.
Sources & evidence
- ORD record
- ord-114c73b4cf6d48f1912639f5dded0dba
- Source dataset
- uspto-grants-1990_09
- Patent number
- US04954508
Reaction notes
Loading…