3,9-二甲氧基-5,8,13,13alpha-四氢-6H-异喹啉并[3,2-a]异喹啉-2,10-二醇合成路线 (共 34 条)
反应条件
1: [[(η6-p-cymene)((1S,2S)-N-p-toluenesulfonyl-1,2-diphenylethylenediamine)]Ru]; formic acid; triethylamine / N,N-dimethyl-formamide / 20 °C 2: water; sodium hydroxide / ethanol / 3 h / 20 °C 3: thionyl chloride / dichloromethane / 1.5 h / 0 - 20 °C 4: sodium hydrogencarbonate / dichloromethane / 1.5 h / 20 °C 5: hydrogenchloride / water; ethanol / 2 h / |Reflux View Scheme
参考文献
Bioorganic and Medicinal Chemistry, , vol. 21, # 4 p. 856 - 868
反应条件
1: water; sodium hydroxide / ethanol / 3 h / 20 °C 2: thionyl chloride / dichloromethane / 1.5 h / 0 - 20 °C 3: sodium hydrogencarbonate / dichloromethane / 1.5 h / 20 °C 4: hydrogenchloride / water; ethanol / 2 h / |Reflux View Scheme
参考文献
Bioorganic and Medicinal Chemistry, , vol. 21, # 4 p. 856 - 868
反应条件
1: thionyl chloride / dichloromethane / 1.5 h / 0 - 20 °C 2: sodium hydrogencarbonate / dichloromethane / 1.5 h / 20 °C 3: hydrogenchloride / water; ethanol / 2 h / |Reflux View Scheme
参考文献
Bioorganic and Medicinal Chemistry, , vol. 21, # 4 p. 856 - 868
反应条件
1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / |Reflux 2: ethanol / 14 h / |Reflux 3: pyridine / dichloromethane / 1.5 h / 0 - 20 °C 4: trichlorophosphate / acetonitrile / 1 h / |Reflux; |Inert atmosphere 5: [[(η6-p-cymene)((1S,2S)-N-p-toluenesulfonyl-1,2-diphenylethylenediamine)]Ru]; formic acid; triethylamine / N,N-dimethyl-formamide / 20 °C 6: water; sodium hydroxide / ethanol / 3 h / 20 °C 7: thionyl chloride / dichloromethane / 1.5 h / 0 - 20 °C 8: sodium hydrogencarbonate / dichloromethane / 1.5 h / 20 °C 9: hydrogenchloride / water; ethanol / 2 h / |Reflux View Scheme
参考文献
Bioorganic and Medicinal Chemistry, , vol. 21, # 4 p. 856 - 868