6,7-二(氮丙啶-1-基)-4-(3-二甲基氨基丙基氨基)喹唑啉-5,8-二酮合成路线 (共 5 条)
反应条件
1: 95 percent / NEt3 / ethanol / 24 h / Ambient temperature 2: 90 percent / H2 / 10percent Pd/C / dioxane; methanol / 760 Torr / Ambient temperature 3: 51 percent / KH2PO4, (KSO3)2NO / methanol; H2O / 4 h 4: 35 percent / 4.5 h / 0 °C View Scheme
参考文献
Journal of Medicinal Chemistry, , vol. 34, # 1 p. 38 - 46
反应条件
1: 90 percent / H2 / 10percent Pd/C / dioxane; methanol / 760 Torr / Ambient temperature 2: 51 percent / KH2PO4, (KSO3)2NO / methanol; H2O / 4 h 3: 35 percent / 4.5 h / 0 °C View Scheme
参考文献
Journal of Medicinal Chemistry, , vol. 34, # 1 p. 38 - 46
反应条件
1: 95 percent / NEt3 / ethanol / 24 h / Ambient temperature 2: 90 percent / H2 / 10percent Pd/C / dioxane; methanol / 760 Torr / Ambient temperature 3: 51 percent / KH2PO4, (KSO3)2NO / methanol; H2O / 4 h 4: 35 percent / 4.5 h / 0 °C View Scheme
参考文献
Journal of Medicinal Chemistry, , vol. 34, # 1 p. 38 - 46
反应条件
1: 51 percent / KH2PO4, (KSO3)2NO / methanol; H2O / 4 h 2: 35 percent / 4.5 h / 0 °C View Scheme
参考文献
Journal of Medicinal Chemistry, , vol. 34, # 1 p. 38 - 46
参考文献
Journal of Medicinal Chemistry, , vol. 34, # 1 p. 38 - 46