2-Chloro-4,6-dimethyl-3-nitropyridine → 1-{4-[(4,6-Dimethyl-3-nitro-2-pyridinyl)amino]phenyl}-2-propanol
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH:9]([OH:11])[CH3:10])=[CH:4][CH:3]=1.Cl[C:13]1[C:18]([N+:19]([O-:21])=[O:20])=[C:17]([CH3:22])[CH:16]=[C:15]([CH3:23])[N:14]=1>>[CH3:22][C:17]1[CH:16]=[C:15]([CH3:23])[N:14]=[C:13]([NH:1][C:2]2[CH:3]=[CH:4][C:5]([CH2:8][CH:9]([OH:11])[CH3:10])=[CH:6][CH:7]=2)[C:18]=1[N+:19]([O-:21])=[O:20]Participants
3
Procedure
The title compound was prepared according to the procedure described in step 3 of Example 1 from 1-(4-aminophenyl)-2-propanol (step 1) and 2-chloro-4,6-dimethyl-3-nitropyridine (step 2 of Example 1).
Sources & evidence
- ORD record
- ord-12a97445d6b64cc18d6ee8dc94919341
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07479564B2
Reaction notes
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