反应详情

A 15 mL round bottom flask was charged with (+)-(4aR)-(10bR)-4-methyl-8-mercapto-10b-methyl-1,2,3,4,4a,-5,6,10b-octahydrobenzo[f]quinolin-3-one (100 mg, 0.38 mmol), potassium carbonate (158 mg, 1.14 mmol), 2-chloro-8-nitro- quinoline (96 mg, 0.46 mmol) and 1.5 mL of anhydrous dimethylformamide, fitted with a reflux condenser, and the stirred mixture was heated at 60°, under nitrogen, for 48 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 (80-100% ethyl acetate/hexanes eluent) to give 90 mg (55%) of the title compound as a solid. mp 199°-200°. FDMS: m/e=433. α[D]589 =+76.80 (c=0.42, chloroform).

1. customfitted with a reflux condenser
2. temperaturethe stirred mixture was heated at 60°, under nitrogen, for 48 h
3. temperatureThe mixture was cooled
4. washwashed with brine (2×25 mL)
5. dry with materialThe combined organic extracts were dried over sodium sulfate
6. concentrationconcentrated
7. custompurified by silica gel chromatography (80-100% ethyl acetate/hexanes eluent)