Cyclohexanemethanol → 4-Bromo-3-(cyclohexylmethoxy)-N-methyl-2-nitroaniline
Reaction equation
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([NH:6][CH3:7])=[C:4]([N+:10]([O-:12])=[O:11])[C:3]=1F.[CH:14]1([CH2:20][OH:21])[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1>>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([NH:6][CH3:7])=[C:4]([N+:10]([O-:12])=[O:11])[C:3]=1[O:21][CH2:20][CH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1Participants
3
Procedure
This compound was synthesized according to the procedure of Example 11, Step 1, using 4-bromo-3-fluoro-N-methyl-2-nitroaniline and cyclohexanemethanol as the starting materials. LCMS calculated for C14H20BrN2O3 (M+H)+: m/z=343.1, 345.1. found: 343.0, 345.1.
Workup
- customThis compound was synthesized
Sources & evidence
- ORD record
- ord-f282bd17319a4a07a980abc584e2a5d6
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09399640B2
Reaction notes
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