1-Iodopropane → N-(2,4-difluorobenzyl)-2-methyl-3-nitro-N-(4-propoxybenzyl)aniline
Reaction equation
[F:1][C:2]1[CH:27]=[C:26]([F:28])[CH:25]=[CH:24][C:3]=1[CH2:4][N:5]([CH2:16][C:17]1[CH:22]=[CH:21][C:20]([OH:23])=[CH:19][CH:18]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[C:7]=1[CH3:15].I[CH2:30][CH2:31][CH3:32]>>[F:1][C:2]1[CH:27]=[C:26]([F:28])[CH:25]=[CH:24][C:3]=1[CH2:4][N:5]([CH2:16][C:17]1[CH:22]=[CH:21][C:20]([O:23][CH2:30][CH2:31][CH3:32])=[CH:19][CH:18]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[C:7]=1[CH3:15]Participants
3
Procedure
The product from Example 33A and 1-iodopropane were processed as described in Example 33B to provide the title compound.
Sources & evidence
- ORD record
- ord-2755550016e44adb9fee05e62181eec1
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06583180B2
Reaction notes
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