1H-1,2,4-Triazole, 5-bromo-1-methyl- → 2-methoxy-4-(1-methyl-1H-1,2,4-triazol-5-yl)aniline
Reaction equation
Br[C:2]1[N:6]([CH3:7])[N:5]=[CH:4][N:3]=1.[CH3:8][O:9][C:10]1[CH:16]=[C:15](B2OC(C)(C)C(C)(C)O2)[CH:14]=[CH:13][C:11]=1[NH2:12]>>[CH3:8][O:9][C:10]1[CH:16]=[C:15]([C:2]2[N:6]([CH3:7])[N:5]=[CH:4][N:3]=2)[CH:14]=[CH:13][C:11]=1[NH2:12]Participants
3
Procedure
The title compound was prepared according to the method described for Preparation 158 using 5-bromo-1-methyl-1H-1,2,4-triazole and 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline. The residue was purified using Biotage silica gel column chromatography eluting with EtOAc.
Workup
- customThe residue was purified
- washeluting with EtOAc
Sources & evidence
- ORD record
- ord-16ad50d2510c4303bcd7423a063f6ef6
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09409907B2
Reaction notes
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