6-氨基-1-[3,4-二羟基-5-(羟基甲基)四氢呋喃-2-基]-2H-三唑并[4,5-c]吡啶-4-酮合成路线 (共 20 条)
反应条件
1: 99.4 percent / CH2Cl2 / 6.3 h / Ambient temperature
2: 56 percent / thionyl chloride / CH2Cl2; dimethylformamide / 4 h / 25 °C
3: 95.5 percent / hydrogen, triethylamine / 5percent Pd/C / ethyl acetate / 4.5 h / Ambient temperature
4: 283 mg / liq. ammonia / 96 h / Ambient temperature
View Scheme
参考文献
Earl; Townsend
Canadian Journal of Chemistry, 1980 , vol. 58, # 23 p. 2550 - 2561
反应条件
1: 87 percent / manganese dioxide / toluene / 1.) reflux, 3 h, 2.) heating, 5 h
2: 99.4 percent / CH2Cl2 / 6.3 h / Ambient temperature
3: 56 percent / thionyl chloride / CH2Cl2; dimethylformamide / 4 h / 25 °C
4: 95.5 percent / hydrogen, triethylamine / 5percent Pd/C / ethyl acetate / 4.5 h / Ambient temperature
5: 283 mg / liq. ammonia / 96 h / Ambient temperature
View Scheme
参考文献
Earl; Townsend
Canadian Journal of Chemistry, 1980 , vol. 58, # 23 p. 2550 - 2561
反应条件
1: 56 percent / thionyl chloride / CH2Cl2; dimethylformamide / 4 h / 25 °C
2: 95.5 percent / hydrogen, triethylamine / 5percent Pd/C / ethyl acetate / 4.5 h / Ambient temperature
3: 283 mg / liq. ammonia / 96 h / Ambient temperature
View Scheme
参考文献
Earl; Townsend
Canadian Journal of Chemistry, 1980 , vol. 58, # 23 p. 2550 - 2561
反应条件
1: 95.5 percent / hydrogen, triethylamine / 5percent Pd/C / ethyl acetate / 4.5 h / Ambient temperature
2: 283 mg / liq. ammonia / 96 h / Ambient temperature
View Scheme
参考文献
Earl; Townsend
Canadian Journal of Chemistry, 1980 , vol. 58, # 23 p. 2550 - 2561
反应条件
1: (CF3CO)2O; pyridine / tetrahydrofuran / -10 °C
2: NEt3 / methanol
View Scheme
参考文献
Jeselnik, Marjan; Jaksa, Suzana; Kobe, Joze
Croatica Chemica Acta, 2004 , vol. 77, # 1-2 p. 153 - 160
反应条件
1: 86 percent / (CF3CO)2O; pyridine / tetrahydrofuran / 0.13 h / 5 °C
2: 77 percent / NH3 / 17 h / 100 °C
View Scheme
参考文献
Stimac, Anton; Leban, Ivan; Kobe, Joze
Synlett, 1999 , # 7 p. 1069 - 1073
反应条件
1: 54.3 percent / conc. ammonium hydroxide / 8 h / Ambient temperature
2: 78.3 percent / phosphoryl chloride / 1.5 h / Heating
3: 1.) hexamethyldisilazane, ammonium sulfate; 2.) stannic chloride / 1.) reflux, 15 h; 2.) 1,2-dichloroethane, 20 h, r.t.
4: 37 percent / liquid ammonia / 15 h / 100 °C / in a steel bomb
View Scheme
参考文献
Meyer Jr.; Revankar; Cook; et al.
Journal of Heterocyclic Chemistry, 1980 , vol. 17, # 1 p. 159 - 169
反应条件
1: 1.) hexamethyldisilazane, ammonium sulfate; 2.) stannic chloride / 1.) reflux, 15 h; 2.) 1,2-dichloroethane, 20 h, r.t.
2: 37 percent / liquid ammonia / 15 h / 100 °C / in a steel bomb
View Scheme
参考文献
Meyer Jr.; Revankar; Cook; et al.
Journal of Heterocyclic Chemistry, 1980 , vol. 17, # 1 p. 159 - 169
反应条件
1: 1.) hexamethyldisilazane, ammonium sulfate; 2.) stannic chloride / 1.) reflux, 15 h; 2.) 1,2-dichloroethane, 20 h, r.t.
2: 37 percent / liquid ammonia / 15 h / 100 °C / in a steel bomb
View Scheme
参考文献
Meyer Jr.; Revankar; Cook; et al.
Journal of Heterocyclic Chemistry, 1980 , vol. 17, # 1 p. 159 - 169
反应条件
1: 78.3 percent / phosphoryl chloride / 1.5 h / Heating
2: 1.) hexamethyldisilazane, ammonium sulfate; 2.) stannic chloride / 1.) reflux, 15 h; 2.) 1,2-dichloroethane, 20 h, r.t.
3: 37 percent / liquid ammonia / 15 h / 100 °C / in a steel bomb
View Scheme
参考文献
Meyer Jr.; Revankar; Cook; et al.
Journal of Heterocyclic Chemistry, 1980 , vol. 17, # 1 p. 159 - 169