Potassium Carbonate → HCID 14552913, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH2:17][C:16](=[O:18])[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][C:14]=3[C:19]([F:22])([F:21])[F:20])[N:9]=2)=[CH:4][CH:3]=1.Cl[CH2:24][C:25]([N:27]1[CH2:32][CH2:31][O:30][CH2:29][CH2:28]1)=[O:26].C(=O)([O-])[O-].[K+].[K+]>CC(=O)CC>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:17]=[C:16]([O:18][CH2:24][C:25]([N:27]3[CH2:32][CH2:31][O:30][CH2:29][CH2:28]3)=[O:26])[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][C:14]=3[C:19]([F:22])([F:20])[F:21])[N:9]=2)=[CH:6][CH:7]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The procedure is as in Example 1, but starting with 2-(4-chlorophenyl)-5-trifluoromethyl-4-quinolone (2.9 g), 4-(2-chloroacetyl)morpholine (1.62 g) and anhydrous potassium carbonate (2.5 g) in 2-butanone (60 cc). After recrystallization in acetonitrile, 4-{[2-(4-chlorophenyl)-5-trifluoromethyl-4-quinolyl]oxyacetyl}morphline (3.2 g), m.p. 179° C., is isolated.
Workup
- customAfter recrystallization in acetonitrile
Sources & evidence
- ORD record
- ord-c3c1a2e5d1a94866a1c1e6b9c1b96dbe
- Source dataset
- uspto-grants-1991_05
- Patent number
- US05017576
Reaction notes
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