2-Methyl-3-nitroaniline → N-{4-[3-(allyloxy)-5-methoxyphenoxy]benzyl}-N-(2-methyl-3-nitrophenyl)amine
Reaction equation
[CH2:1]([O:4][C:5]1[CH:6]=[C:7]([CH:17]=[C:18]([O:20][CH3:21])[CH:19]=1)[O:8][C:9]1[CH:16]=[CH:15][C:12]([CH:13]=O)=[CH:11][CH:10]=1)[CH:2]=[CH2:3].[CH3:22][C:23]1[C:29]([N+:30]([O-:32])=[O:31])=[CH:28][CH:27]=[CH:26][C:24]=1[NH2:25]>>[CH2:1]([O:4][C:5]1[CH:6]=[C:7]([CH:17]=[C:18]([O:20][CH3:21])[CH:19]=1)[O:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13][NH:25][C:24]2[CH:26]=[CH:27][CH:28]=[C:29]([N+:30]([O-:32])=[O:31])[C:23]=2[CH3:22])=[CH:11][CH:10]=1)[CH:2]=[CH2:3]Participants
3
Procedure
The product from Example 90B and 2-methyl-3-nitroaniline were processed as in Example 6A to provide the title compound. MS (ESI−) m/z 419 (M−H)−.
Sources & evidence
- ORD record
- ord-441fadc684f14bd7af996ec8d496ea9d
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06583180B2
Reaction notes
Loading…