2-[2-(5-溴-1H-吲哚-3-基)乙基]-3-[3-(1-甲基乙氧基)苯基]-4-(3H-)-喹唑啉酮合成路线 (共 4 条)
反应条件
1: 86 percent / K2CO3 / acetone / Heating 2: 7.08 g / H2 / PtO2 / ethanol / 1.5 h / 2068.6 Torr / Ambient temperature 3: 83 percent / 2 h / 90 °C 4: 36 percent / pyridinium p-toluenesulfonate / pyridine / 84 h / Heating View Scheme
参考文献
Yu; Thrasher; McCowan; Mason; Mendelsohn
Journal of Medicinal Chemistry, 1991 , vol. 34, # 4 p. 1505 - 1508
反应条件
1: 7.08 g / H2 / PtO2 / ethanol / 1.5 h / 2068.6 Torr / Ambient temperature 2: 83 percent / 2 h / 90 °C 3: 36 percent / pyridinium p-toluenesulfonate / pyridine / 84 h / Heating View Scheme
参考文献
Yu; Thrasher; McCowan; Mason; Mendelsohn
Journal of Medicinal Chemistry, 1991 , vol. 34, # 4 p. 1505 - 1508
反应条件
pyridinium p-toluenesulfonate in pyridine 84 h; Heating;
参考文献
Yu; Thrasher; McCowan; Mason; Mendelsohn
Journal of Medicinal Chemistry, 1991 , vol. 34, # 4 p. 1505 - 1508
反应条件
1: 83 percent / 2 h / 90 °C 2: 36 percent / pyridinium p-toluenesulfonate / pyridine / 84 h / Heating View Scheme
参考文献
Yu; Thrasher; McCowan; Mason; Mendelsohn
Journal of Medicinal Chemistry, 1991 , vol. 34, # 4 p. 1505 - 1508