3-Isopropylaniline → 4-bromo-N-(3-isopropylphenyl)picolinamide
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C:8]([OH:10])=O)[CH:3]=1.[CH:11]([C:14]1[CH:15]=[C:16]([CH:18]=[CH:19][CH:20]=1)[NH2:17])([CH3:13])[CH3:12]>>[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C:8]([NH:17][C:16]2[CH:18]=[CH:19][CH:20]=[C:14]([CH:11]([CH3:13])[CH3:12])[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 3-isopropylaniline were converted to the title compound.
Sources & evidence
- ORD record
- ord-3700250d417745dda7e04a14ad50b4e0
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08889870B2
Reaction notes
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