Reaction equation
[F:1][C:2]1[C:10]([CH:11]=[O:12])=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[N:5][NH:6]2.[Cl:13][C:14]1[CH:21]=[CH:20][C:17]([CH2:18]Br)=[C:16]([C:22]([F:25])([F:24])[F:23])[CH:15]=1>>[Cl:13][C:14]1[CH:21]=[CH:20][C:17]([CH2:18][N:6]2[C:7]3[C:3](=[C:2]([F:1])[C:10]([CH:11]=[O:12])=[CH:9][CH:8]=3)[CH:4]=[N:5]2)=[C:16]([C:22]([F:23])([F:24])[F:25])[CH:15]=1Participants
3
Procedure
[4-Chloro-2-(trifluoromethyl)benzyl]-4-fluoro-1H-indazol-5-carbaldehyde was prepared from 4-fluoro-1H-indazole-5-carbaldehyde and 4-chloro-2-(trifluoromethyl)benzyl bromide following General Procedure A.
Sources & evidence
- ORD record
- ord-56ae487af324456d86c0898b0aa135cd
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08796256B2
Linked notes
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