3-(3-Ethoxy-4-nitrophenyl)-4-methyl-4H-1,2,4-triazole → 2-Ethoxy-4-(4-methyl-4H-1,2,4-triazol-3-yl)aniline
Reaction equation
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([C:13]2[N:17]([CH3:18])[CH:16]=[N:15][N:14]=2)[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)[CH3:2]>CCOC(C)=O.CCO>[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([C:13]2[N:17]([CH3:18])[CH:16]=[N:15][N:14]=2)[CH:7]=[CH:8][C:9]=1[NH2:10])[CH3:2]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
The title compound was prepared according to the method described for Preparation 107 using 3-(3-Ethoxy-4-nitrophenyl)-4-methyl-4H-1,2,4-triazole (Preparation 116) in EtOAc and EtOH (1:8 v:v).
Sources & evidence
- ORD record
- ord-f35e0841564844e4be4e1850f274898a
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09334286B2
Reaction notes
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