3-氨基-1-甲基-5H-吡啶[4,3-b]吲哚合成路线 (共 19 条)
反应条件
1: 20percent aqueous NaOH / ethanol / 12 h / Heating 2: 86 percent / diethyl ether; methanol; CHCl3 / 0.17 h / 0 °C 3: 86 percent / AcOH, polyphosphoric acid / acetonitrile / 12 h / Ambient temperature 4: 77 percent / NH2OH*HCl, NaOAc / ethanol / 1 h / Heating 5: 51 percent / xylene / 24 h / Heating 6: 95 percent / 10percent aqueous NaOH / ethanol / 1 h / Heating 7: 98 percent / diphenylphosphoryl azide (DPPA), triethylamine / 0.5 h / 80 °C 8: 81 percent / AcOH / H2O / 1 h / 80 °C View Scheme
参考文献
Journal of Organic Chemistry, , vol. 57, # 22 p. 5917 - 5921
反应条件
1: 1.5 h / 180 °C 2: 20percent aqueous NaOH / ethanol / 12 h / Heating 3: 86 percent / diethyl ether; methanol; CHCl3 / 0.17 h / 0 °C 4: 86 percent / AcOH, polyphosphoric acid / acetonitrile / 12 h / Ambient temperature 5: 77 percent / NH2OH*HCl, NaOAc / ethanol / 1 h / Heating 6: 51 percent / xylene / 24 h / Heating 7: 95 percent / 10percent aqueous NaOH / ethanol / 1 h / Heating 8: 98 percent / diphenylphosphoryl azide (DPPA), triethylamine / 0.5 h / 80 °C 9: 81 percent / AcOH / H2O / 1 h / 80 °C View Scheme
参考文献
Journal of Organic Chemistry, , vol. 57, # 22 p. 5917 - 5921
反应条件
1: 20percent aqueous NaOH / ethanol / 14 h / Heating 2: pyridine / 12 h / Heating 3: 86 percent / diethyl ether; methanol; CHCl3 / 0.17 h / 0 °C 4: 86 percent / AcOH, polyphosphoric acid / acetonitrile / 12 h / Ambient temperature 5: 77 percent / NH2OH*HCl, NaOAc / ethanol / 1 h / Heating 6: 51 percent / xylene / 24 h / Heating 7: 95 percent / 10percent aqueous NaOH / ethanol / 1 h / Heating 8: 98 percent / diphenylphosphoryl azide (DPPA), triethylamine / 0.5 h / 80 °C 9: 81 percent / AcOH / H2O / 1 h / 80 °C View Scheme
参考文献
Journal of Organic Chemistry, , vol. 57, # 22 p. 5917 - 5921
反应条件
1: 98 percent / diphenylphosphoryl azide (DPPA), triethylamine / 0.5 h / 80 °C 2: 81 percent / AcOH / H2O / 1 h / 80 °C View Scheme
参考文献
Journal of Organic Chemistry, , vol. 57, # 22 p. 5917 - 5921
反应条件
aluminium trichloride T=100 - 120°C; 12 h;
参考文献
Takeda; Shudo; Okamoto; Kosuge
Chemical and Pharmaceutical Bulletin, 1981 , vol. 29, # 5 p. 1280 - 1285
反应条件
1: 40 percent / (CF3CO)2O; CF3COOH; H2O2 / Mo(CO)6 / CH2Cl2 / cooling
2: 96 percent / hydrazine monohydrate / Pd/C / tetrahydrofuran / 1 h / -20 °C
3: 37 percent / triethylamine / tetrahydrofuran / 0.5 h / -20 - 0 °C
4: 91 percent / triethylamine / tetrahydrofuran / 1 h / 0 °C
5: acetonitrile; H2O / 20 °C / pH 7.0
View Scheme
参考文献
Rajagopal, Sridharan; Brooks, Michael E.; Nguyen, Thach-Mien; Novak, Michael
Tetrahedron, 2003 , vol. 59, # 40 p. 8003 - 8010
反应条件
triethylamine in tetrahydrofuran
T=-20 - 0°C; 0.5 h;
参考文献
Rajagopal, Sridharan; Brooks, Michael E.; Nguyen, Thach-Mien; Novak, Michael
Tetrahedron, 2003 , vol. 59, # 40 p. 8003 - 8010
反应条件
1: 40 percent / (CF3CO)2O; CF3COOH; H2O2 / Mo(CO)6 / CH2Cl2 / cooling
2: 96 percent / hydrazine monohydrate / Pd/C / tetrahydrofuran / 1 h / -20 °C
View Scheme
参考文献
Rajagopal, Sridharan; Brooks, Michael E.; Nguyen, Thach-Mien; Novak, Michael
Tetrahedron, 2003 , vol. 59, # 40 p. 8003 - 8010
反应条件
dihydrogen peroxide; trifluoroacetic acid; trifluoroacetic anhydride; hexacarbonyl molybdenum in dichloromethane
cooling;
参考文献
Rajagopal, Sridharan; Brooks, Michael E.; Nguyen, Thach-Mien; Novak, Michael
Tetrahedron, 2003 , vol. 59, # 40 p. 8003 - 8010