Benzophenone imine → 5-((Diphenylmethylene)amino)-N-methoxy-N-methylnicotinamide
Reaction equation
Br[C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH:13]=1)[C:7]([N:9]([O:11][CH3:12])[CH3:10])=[O:8].[C:14](=[NH:27])([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[C:15]1([C:14](=[N:27][C:2]2[CH:3]=[N:4][CH:5]=[C:6]([CH:13]=2)[C:7]([N:9]([O:11][CH3:12])[CH3:10])=[O:8])[C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1Participants
3
Procedure
Prepared according to the method described for Preparation 51 using 5-bromo-N-methoxy-N-methylnicotinamide and benzophenone imine.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-6fc6a15f1db74d5eace8a90604b569c1
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09163021B2
Reaction notes
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