Dimethylamine → [2-[[3-(Dimethylamino)propyl](3-nitro-2-pyridinyl)amino]phenyl]phenylmethanone
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][N:5]([C:14]1[C:19]([N+:20]([O-:22])=[O:21])=[CH:18][CH:17]=[CH:16][N:15]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[CH:12]=[O:13].[CH3:23][NH:24][CH3:25]>>[CH3:23][N:24]([CH3:25])[CH2:2][CH2:3][CH2:4][N:5]([C:14]1[C:19]([N+:20]([O-:22])=[O:21])=[CH:18][CH:17]=[CH:16][N:15]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[C:12]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:13]Participants
3
Procedure
The title compound is prepared by reacting [2-[[3-chloropropyl](3-nitro-2-pyridinyl)amino]phenyl]methanone with dimethylamine.
Sources & evidence
- ORD record
- ord-9b000b37c4774f728c19a28178517494
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04480100
Reaction notes
Loading…