反应条件
1.1: 79 percent / lithium triethylborohydride / dimethylsulfoxide / 1 h / 65 °C 2.1: 93 percent / H2 / Pd/C / CH2Cl2; methanol / 20 °C 3.1: pyridine / 5 h / Heating 4.1: 4-(dimethylamino)pyridine / CH2Cl2 / 2 h / 20 °C 5.1: 69 percent / HCl / acetone; methanol / 2 h / 60 °C 6.1: 95 percent / pyridinium chlorochromate / CH2Cl2 / 1 h / 20 °C 7.1: 77 percent / NaOH / methanol; tetrahydrofuran / 3 h / 20 °C 8.1: NH2NH2*H2O / bis-(2-hydroxy-ethyl) ether; ethanol / 1 h / Heating; Huang-Minlon reduction 8.2: 77 percent / KOH / 2 h / Heating View Scheme
参考文献
Sasaki, Kazue; Minowa, Nobuto; Kuzuhara, Hiroyuki; Nishiyama, Shoji
Bioorganic and Medicinal Chemistry, 2005 , vol. 13, # 16 p. 4900 - 4911