2-Chloro-4,6-dimethyl-3-nitropyridine → (2S)-1-{4-[(4,6-dimethyl-3-nitro-2-pyridinyl)amino]phenyl}-2-propanol
Reaction equation
Cl[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[C:6]([CH3:11])[CH:5]=[C:4]([CH3:12])[N:3]=1.[NH2:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][C@@H:21]([OH:23])[CH3:22])=[CH:16][CH:15]=1>>[CH3:11][C:6]1[CH:5]=[C:4]([CH3:12])[N:3]=[C:2]([NH:13][C:14]2[CH:15]=[CH:16][C:17]([CH2:20][C@@H:21]([OH:23])[CH3:22])=[CH:18][CH:19]=2)[C:7]=1[N+:8]([O-:10])=[O:9]Participants
3
Procedure
The title compound was prepared according to the procedure described in step 1 of Example 162 from 2-chloro-4,6-dimethyl-3-nitropyridine (step 2 of Example 1) and (2S)-1-(4-aminophenyl)-2-propanol (step 2 of Example 248).
Sources & evidence
- ORD record
- ord-46fb849066174de5bbbbdb966bc22ade
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07141580B2
Reaction notes
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