4-(Trifluoromethyl)aniline → 4-Bromo-N-(4-(trifluoromethyl)phenyl)picolinamide
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C:8]([OH:10])=O)[CH:3]=1.[F:11][C:12]([F:21])([F:20])[C:13]1[CH:19]=[CH:18][C:16]([NH2:17])=[CH:15][CH:14]=1>>[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C:8]([NH:17][C:16]2[CH:18]=[CH:19][C:13]([C:12]([F:11])([F:20])[F:21])=[CH:14][CH:15]=2)=[O:10])[CH:3]=1Participants
3
Procedure
In a manner similar to that describe in Preparation 34, 4-bromo-pyridine-2-carboxylic acid and 4-trifluoromethylaniline were converted to the title compound.
Sources & evidence
- ORD record
- ord-f0fcf294d6a94539900a37bf15c7b7e3
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09388176B2
Reaction notes
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