2-Bromoisonicotinic acid → 2-Bromo-N-(3-isopropyl-phenyl)-isonicotinamide
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][N:10]=1)[C:5]([OH:7])=O.[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:3]=[C:4]([CH:8]=[CH:9][N:10]=1)[C:5]([NH:17][C:16]1[CH:18]=[CH:19][CH:20]=[C:14]([CH:11]([CH3:13])[CH3:12])[CH:15]=1)=[O:7]Participants
3
Procedure
In a manner similar to that described in Preparation 17, 2-bromoisonicotinic acid and 3-isopropylaniline were converted to the title compound
Sources & evidence
- ORD record
- ord-ecc50646aba745e08aaf54ae098e3393
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09388176B2
Reaction notes
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