S-3-N-BOC-3-(甲氨基)哌啶合成路线 (共 4 条)
反应条件
1: tert-butyl (3S)-1-(trifluoroacetyl)piperidinylcarbamate With sodium hydride in tetrahydrofuran T=0°C; 0.333333 h; 2: methyl iodide in tetrahydrofuran T=0 - 20°C; 4 h; 3: With potassium carbonate in methanol T=20°C; 16 h;
参考文献
ABBOTT LABORATORIES
Patent: EP1428824 A1, 2004 ;
Location in patent: Page 45 ;
反应条件
hydrogen; palladium 10 on activated carbon in methanol 2 h;
参考文献
WO2012/58645 A1, ;
Page/Page column 135 ;
WO 2012/058645 A1
反应条件
1.1: triethylamine / dichloromethane / 0 - 20 °C 2.1: sodium hydride / N,N-dimethyl-formamide; paraffin oil (nujol) / 0 °C 2.2: 4 h / 20 °C 3.1: hydrogen / palladium 10 on activated carbon / methanol / 2 h View Scheme
参考文献
WO2012/58645 A1, ;
WO 2012/058645 A1
反应条件
1.1: sodium hydride / N,N-dimethyl-formamide; paraffin oil (nujol) / 0 °C 1.2: 4 h / 20 °C 2.1: hydrogen / palladium 10 on activated carbon / methanol / 2 h View Scheme
参考文献
WO2012/58645 A1, ;
WO 2012/058645 A1