p-Fluoronitrobenzene → 1-Boc-4-(4-Nitrophenyl)piperazine
Reaction equation
F[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][CH:3]=1.[C:11]([N:18]1[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]1)([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12]>>[N+:8]([C:5]1[CH:6]=[CH:7][C:2]([N:21]2[CH2:20][CH2:19][N:18]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH2:23][CH2:22]2)=[CH:3][CH:4]=1)([O-:10])=[O:9]Participants
3
Procedure
Following Example 188a, 1-fluoro-4-nitrobenzene (2.8 g, 20 mmol) and N-Boc-piperazine (11 g, 60 mmol) were reacted to give 327a as a yellow solid (3 g, 51%). MS: [M+H]+ 308.
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-3a52baefa42f4fcaa6113d0732ae41e4
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08618107B2
Reaction notes
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