4-Fluoroaniline → HCID 178448107, compound
Reaction equation
[CH:1]([C@@H:4]1[CH2:9][CH2:8][C@H:7]([N:10]2[CH2:15][CH2:14][C:13](=O)[CH2:12][CH2:11]2)[CH2:6][CH2:5]1)([CH3:3])[CH3:2].[F:17][C:18]1[CH:24]=[CH:23][C:21]([NH2:22])=[CH:20][CH:19]=1>CCCCC>[F:17][C:18]1[CH:24]=[CH:23][C:21]([N:22]=[C:13]2[CH2:14][CH2:15][N:10]([C@H:7]3[CH2:8][CH2:9][C@@H:4]([CH:1]([CH3:3])[CH3:2])[CH2:5][CH2:6]3)[CH2:11][CH2:12]2)=[CH:20][CH:19]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
cis-1-(4-Isopropyl-cyclohexyl)-piperidine-4-on (5.0 g, 23.4 mmol), 4-fluoro aniline (3.3 g, 35.3 mmol) and molecular sieves (20 g, 4A) were stirred in 100 ml pentane at room temperature for 6 days. The molecular sieves was filtered off and the solvent was evaporated. The crude product was used without any further purification for the following step.
Workup
- filtrationThe molecular sieves was filtered off
- customthe solvent was evaporated
- customThe crude product was used without any further purification for the following step
Sources & evidence
- ORD record
- ord-049100d7eee149a2a1401959d30f5d11
- Source dataset
- uspto-grants-2000_06
- Patent number
- US06075034
Reaction notes
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