Morpholine → HCID 66917331, compound
Reaction equation
[F:1][C:2]1[CH:11]=[CH:10][C:9]([O:12][CH2:13][CH2:14][CH3:15])=[C:8]2[C:3]=1[C:4](=[O:25])[C:5]([C:16]1[CH:24]=[CH:23][C:19]([C:20](O)=[O:21])=[CH:18][CH:17]=1)=[CH:6][NH:7]2.[NH:26]1[CH2:31][CH2:30][O:29][CH2:28][CH2:27]1.CCN=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1>CN(C=O)C>[F:1][C:2]1[CH:11]=[CH:10][C:9]([O:12][CH2:13][CH2:14][CH3:15])=[C:8]2[C:3]=1[C:4](=[O:25])[C:5]([C:16]1[CH:17]=[CH:18][C:19]([C:20]([N:26]3[CH2:31][CH2:30][O:29][CH2:28][CH2:27]3)=[O:21])=[CH:23][CH:24]=1)=[CH:6][NH:7]2Participants
6
Procedure
4-(5-Fluoro-4-oxo-8-propoxy-1,4-dihydroquinolin-3-yl)benzoic acid (260 mg, 0.76 mmol), morpholine (99.5 mg, 1.14 mmol), WSC (189 mg, 0.99 mmol) and HOBT (151 mg, 0.99 mmol) were added to DMF (10 ml), and the mixture was stirred at room temperature for 15 hours. The reaction mixture was concentrated under reduced pressure, and the residue was then purified by silica gel column chromatography (dichloromethane:methanol=30:1). The purified product was concentrated under reduced pressure, and the residue was recrystallized from ethyl acetate to thereby obtain 80 mg of powdery white 5-fluoro-3-[4-(morpholine-4-carbonyl)phenyl]-8-propoxy-1H-quinolin-4-one (yield: 26%).
Workup
- concentrationThe reaction mixture was concentrated under reduced pressure
- customthe residue was then purified by silica gel column chromatography (dichloromethane:methanol=30:1)
- concentrationThe purified product was concentrated under reduced pressure
- customthe residue was recrystallized from ethyl acetate
Sources & evidence
- ORD record
- ord-5d144095b3fb416aaae930d73b0b2214
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08642619B2
Reaction notes
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