Tetrahydrofuran → HCID 54222450, compound
Reaction equation
Br[C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][CH:8]=[CH:7]2.[C:12](=[O:15])([O-])[O-].[Na+].[Na+].[CH2:18]1[CH2:22]O[CH2:20][CH2:19]1>C(OCC)(=O)C.[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH3:11][N:10]1[C@H:9]2[C@@:18]([CH3:22])([C:18]3[CH:22]=[CH:4][C:3]([C:2]4[CH:3]=[CH:4][CH:5]=[C:6]5[C:11]=4[N:10]=[CH:9][CH:8]=[CH:7]5)=[CH:2][C:19]=3[CH2:20][CH2:8]2)[CH2:19][CH2:20][C:12]1=[O:15]Participants
Procedure
A 15 mL round bottom flask was charged with (+)-(4aR)-(10bR)-4-methyl-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one-8-boronic acid (178 mg, 0.65 mmol), tetrakis(triphenylphosphine) palladium (0) (23 mg, 0.02 mmol), 8-bromoquinoline (135 mg, 0.65 mmol), 0.65 mL of 2M sodium carbonate and 2 mL of THF, fitted with a reflux condenser, and the stirred mixture was heated at 80°, under nitrogen, for 24 h. The mixture was cooled, diluted with ethyl acetate (75 mL) and washed with brine (2×25 mL). The combined organic extracts were dried over sodium sulfate, concentrated, and purified by silica gel chromatography (ethyl acetate eluent) to give 88 mg (38%) of the title compound as a tan solid. mp 205°-207°. FDMS: m/e=356 α[D]589 =+76.28 (c=0.47, chloroform).
Workup
- customfitted with a reflux condenser
- temperaturethe stirred mixture was heated at 80°, under nitrogen, for 24 h
- temperatureThe mixture was cooled
- washwashed with brine (2×25 mL)
- dry with materialThe combined organic extracts were dried over sodium sulfate
- concentrationconcentrated
- custompurified by silica gel chromatography (ethyl acetate eluent)
Sources & evidence
- ORD record
- ord-530a442890e14618be2b407d88bbb2ca
- Source dataset
- uspto-grants-1997_05
- Patent number
- US05629007
Reaction notes
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