2-Methyl-3-nitroaniline → HCID 18512121, compound
Reaction equation
[CH2:1]([O:4][C:5]1[CH:6]=[C:7]([CH:17]=[CH:18][C:19]=1[CH2:20][CH3:21])[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]=[CH:18][C:19]=1[CH2:20][CH3:21])[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 236C and 2-methyl-3-nitroaniline were processed as in Example 6A to provide the titled compound. MS (ESI−) m/z 423 (M−H)−.
Sources & evidence
- ORD record
- ord-7fe93410cb4d4feb8c9c2f2415d3d152
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06583180B2
Reaction notes
Loading…