1H-Indazole-5-carboxaldehyde → 1-(4-Bromo-2-trifluoromethyl-benzyl)-1H-indazole-5-carbaldehyde
Reaction equation
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6]Br)=[C:4]([C:10]([F:13])([F:12])[F:11])[CH:3]=1.[NH:14]1[C:22]2[C:17](=[CH:18][C:19]([CH:23]=[O:24])=[CH:20][CH:21]=2)[CH:16]=[N:15]1>>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][N:14]2[C:22]3[C:17](=[CH:18][C:19]([CH:23]=[O:24])=[CH:20][CH:21]=3)[CH:16]=[N:15]2)=[C:4]([C:10]([F:13])([F:12])[F:11])[CH:3]=1Participants
3
Procedure
[4-Bromo-2-(trifluoromethyl)benzyl]-1H-indazol-5-carbaldehyde was prepared from 4-bromo-2-(trifluoromethyl)benzyl bromide and 1H-indazol-5-carbaldehyde following General Procedure A.
Sources & evidence
- ORD record
- ord-b62730f77f9e4717a625b7e77ae4228c
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08796256B2
Reaction notes
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