p-Fluoronitrobenzene → Ethyl-[1-(4-nitro-phenyl)-pyrrolidin-3-yl]-amine
Reaction equation
[CH2:1]([NH:3][CH:4]1[CH2:8][CH2:7][NH:6][CH2:5]1)[CH3:2].F[C:10]1[CH:15]=[CH:14][C:13]([N+:16]([O-:18])=[O:17])=[CH:12][CH:11]=1>>[CH2:1]([NH:3][CH:4]1[CH2:8][CH2:7][N:6]([C:10]2[CH:15]=[CH:14][C:13]([N+:16]([O-:18])=[O:17])=[CH:12][CH:11]=2)[CH2:5]1)[CH3:2]Participants
3
Procedure
The compound was prepared from 3-ethylamino-pyrolidine (TCI-US) and 4-fluoro-nitrobenzene (Aldrich) following the procedure used in Example 1. MS (m+H)+: 236.
Sources & evidence
- ORD record
- ord-69fb25d19ffc4a788494bd4997b090f4
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07211576B2
Reaction notes
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