2-Methoxy-5-nitrophenol → 4-Methoxy-3-[2-(piperidin-1-yl)ethoxy]aniline
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-])=O)=[CH:5][C:4]=1[OH:12].Cl.Cl[CH2:15][CH2:16][N:17]1[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1>>[N:17]1([CH2:16][CH2:15][O:12][C:4]2[CH:5]=[C:6]([CH:7]=[CH:8][C:3]=2[O:2][CH3:1])[NH2:9])[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1Participants
3
Procedure
The title compound was prepared from 2-methoxy-5-nitrophenol and 1-(2-chloroethyl)piperidine hydrochloride using a similar procedure to Descriptions 1 and 2 (40%).
Sources & evidence
- ORD record
- ord-19ca760363f04f56a6a09df8dae78f87
- Source dataset
- uspto-grants-1998_09
- Patent number
- US05801170
Reaction notes
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