(S)-(-)-1-苄基-3-乙酰氨基吡咯烷合成路线 (共 5 条)
反应条件
1: 84 percent / triethylamine / CH2Cl2 / 1.) 0 deg C, 20 min, 2.) room temperature, 1.5 h 2: 87 percent / tetra-n-butylammonium azide / acetonitrile / 1 h / 65 °C 3: 1.) hydrogen, 2.) pyridine, triethylamine / 1.) methanol, 4 atm, room temperature, 4 h, 2.) room temperature, 16 h View Scheme
参考文献
Journal of Medicinal Chemistry, , vol. 31, # 8 p. 1586 - 1590
反应条件
1: 87 percent / tetra-n-butylammonium azide / acetonitrile / 1 h / 65 °C 2: 1.) hydrogen, 2.) pyridine, triethylamine / 1.) methanol, 4 atm, room temperature, 4 h, 2.) room temperature, 16 h View Scheme
参考文献
Journal of Medicinal Chemistry, , vol. 31, # 8 p. 1586 - 1590
反应条件
1: CF3CO2H / CH2Cl2 2: pyridine View Scheme
参考文献
Synthetic Communications, , vol. 28, # 21 p. 3919 - 3926
反应条件
pyridine; hydrogen; triethylamine 1.) methanol, 4 atm, room temperature, 4 h, 2.) room temperature, 16 h; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
参考文献
Journal of Medicinal Chemistry, , vol. 31, # 8 p. 1586 - 1590
反应条件
pyridine Yield given;
参考文献
Synthetic Communications, , vol. 28, # 21 p. 3919 - 3926