反应详情

温度

130 °C

A stirring mixture of title compound 92 (2 g, 5.06 mmol) in polyphosphoric acid (4.76 ml, 41.7 mmol) was heated at 130° C. for 3 h. The reaction mixture was cooled, diluted with dichloromethane and water and stirred overnight. The layers were separated and the aqueous layer was extracted with dichloromethane. The combined organic layers were washed with brine, dried over MgSO4, filtered and solvent evaporated. The crude residue was purified via ISCO (0-25% Hex/EtOAc; 40 g silica gel column) to afford title compound 93 (125 mg, 6.5%) as a light yellow solid. LRMS (ESI): (calc) 377.11. (found) 378.4 (MH)+.

1. temperatureThe reaction mixture was cooled
2. customThe layers were separated
3. extractionthe aqueous layer was extracted with dichloromethane
4. washThe combined organic layers were washed with brine
5. dry with materialdried over MgSO4
6. filtrationfiltered
7. customsolvent evaporated
8. customThe crude residue was purified via ISCO (0-25% Hex/EtOAc; 40 g silica gel column)