2-(Chloromethyl)-3-(trifluoromethyl)pyridine → 1-(3-Trifluoromethyl-pyridin-2-ylmethyl)-1H-indazole-5-carbaldehyde
Reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([CH:10]=[O:11])=[CH:7][CH:8]=2)[CH:3]=[N:2]1.Cl[CH2:13][C:14]1[C:19]([C:20]([F:23])([F:22])[F:21])=[CH:18][CH:17]=[CH:16][N:15]=1>>[F:23][C:20]([F:21])([F:22])[C:19]1[C:14]([CH2:13][N:1]2[C:9]3[C:4](=[CH:5][C:6]([CH:10]=[O:11])=[CH:7][CH:8]=3)[CH:3]=[N:2]2)=[N:15][CH:16]=[CH:17][CH:18]=1Participants
3
Procedure
1-(3-Trifluoromethyl-pyridin-2-ylmethyl)-1H-indazole-5-carbaldehyde was prepared from 1H-Indazole-5-carbaldehyde and 2-Chloromethyl-3-trifluoromethyl-pyridine following General Procedure A.
Sources & evidence
- ORD record
- ord-0a66159cd68645bf9025b30480ae3241
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399681B2
Reaction notes
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