Cyclobutylcarbinol → 4-Bromo-3-(cyclobutylmethoxy)-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([CH2:18][OH:19])[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:19][CH2:18][CH:14]1[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 cyclobutylmethanol as the starting materials. LCMS calculated for C12H16BrN2O3 (M+H)+: m/z=315.0, 317.0. found: 315.0, 317.0.
Workup
- customThis compound was synthesized
Sources & evidence
- ORD record
- ord-dae2fc49103a4fbfaf3109d5986073d2
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09399640B2
Reaction notes
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