2-Methylbenzylamine → 5-bromo-N-(2-methylbenzyl)nicotinamide
Reaction equation
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH:10]=1)[C:7]([OH:9])=O.[CH3:11][C:12]1[CH:19]=[CH:18][CH:17]=[CH:16][C:13]=1[CH2:14][NH2:15]>>[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH:10]=1)[C:7]([NH:15][CH2:14][C:13]1[CH:16]=[CH:17][CH:18]=[CH:19][C:12]=1[CH3:11])=[O:9]Participants
3
Procedure
Prepared from 5-bromonicotinic acid and 2-methylbenzylamine using procedures as described in Example 1H. MS (APCI) m/z 305, 307 (M+H)+.
Sources & evidence
- ORD record
- ord-99c63a9629254b158c6b6d1279d88249
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08148408B2
Reaction notes
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