Potassium Iodide → HCID 178458489, compound
Reaction equation
[NH:1]1[CH2:6][CH2:5][CH:4]([C:7]2[N:8]=[CH:9][NH:10][CH:11]=2)[CH2:3][CH2:2]1.F[C:13]1[CH:18]=[CH:17][C:16]([C:19](=[O:22])[CH2:20][CH3:21])=[CH:15][CH:14]=1.C(=O)([O-])[O-].[Na+].[Na+].[I-].[K+]>CN(C)C=O.O>[C:19]([C:16]1[CH:17]=[CH:18][C:13]([N:1]2[CH2:2][CH2:3][CH:4]([C:7]3[N:8]=[CH:9][NH:10][CH:11]=3)[CH2:5][CH2:6]2)=[CH:14][CH:15]=1)(=[O:22])[CH2:20][CH3:21]Participants
7
Procedure
3 g (0.019 mole) of 4-(4-piperidyl)-1H-imidazole and 2.88 g (0.019 mole) of para-fluoropropiophenone are stirred in 70 cm3 of dimethylformamide for 5 minutes. 4 g (0.037 mole) of disodium carbonate and 0.2 g (0.0012 mole) of potassium iodide are added and the solution is brought to 160° C. for 3 hours. After being cooled, the solution is poured into 200 cm3 of water and stirred for 1 hour. The precipitate formed is drained, washed with water, dried and recrystallized in acetonitrile.
Workup
- temperatureAfter being cooled
- customThe precipitate formed
- washwashed with water
- customdried
- customrecrystallized in acetonitrile
Sources & evidence
- ORD record
- ord-f87d3afad9354b5ab91c144186471252
- Source dataset
- uspto-grants-1987_11
- Patent number
- US04707487
Reaction notes
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