(2-氯-4-吡啶)-二甲胺合成路线 (共 9 条)
反应条件
1: With n-butyllithium; 2-(dimethylamino)-ethanol in hexane
T=0°C; 1 h;
2: With 1,2,2-trichloro-1,1,2-trichloro-ethane in hexane
T=-78 - 0°C; 1.5 h; Further stages.;
参考文献
Cuperly, David; Gros, Philippe; Fort, Yves
Journal of Organic Chemistry, 2002 , vol. 67, # 1 p. 238 - 241
反应条件
in water
T=50°C; 20 h;
参考文献
Schlosser, Manfred; Bobbio, Carla; Rausis, Thierry
Journal of Organic Chemistry, 2005 , vol. 70, # 7 p. 2494 - 2502
反应条件
in water
T=50°C; 18 h;
参考文献
KALYPSYS, INC.
Patent: WO2009/29617 A1, 2009 ;
Location in patent: Page/Page column 47 ;
WO 2009/029617 A1
反应条件
1: H2NNH2*H2O / tetrahydrofuran / 20 h / 50 °C
2: 6.41 g / tetrabutylammonium fluoride trihydrate / tetrahydrofuran / 2 h / 25 °C
3: 67 percent / CuSO4*5H2O / H2O / 0.75 h / Heating
4: 88 percent / H2O / 20 h / 50 °C
View Scheme
参考文献
Schlosser, Manfred; Bobbio, Carla; Rausis, Thierry
Journal of Organic Chemistry, 2005 , vol. 70, # 7 p. 2494 - 2502
反应条件
1.1: BuLi / tetrahydrofuran; hexane / 0.75 h / -75 °C
1.2: 64 percent / I2 / tetrahydrofuran; hexane / 0.25 h / -75 °C
2.1: isobutylmagnesium chloride / tetrahydrofuran / 0.75 h / 0 °C
2.2: 94 percent / N-chlorosuccinimide / tetrahydrofuran / 0.75 h
3.1: BuLi / tetrahydrofuran; hexane / 0.75 h / -75 °C
3.2: 92 percent / tetrahydrofuran; hexane
4.1: H2NNH2*H2O / tetrahydrofuran / 20 h / 50 °C
5.1: 6.41 g / tetrabutylammonium fluoride trihydrate / tetrahydrofuran / 2 h / 25 °C
6.1: 67 percent / CuSO4*5H2O / H2O / 0.75 h / Heating
7.1: 88 percent / H2O / 20 h / 50 °C
View Scheme
参考文献
Schlosser, Manfred; Bobbio, Carla; Rausis, Thierry
Journal of Organic Chemistry, 2005 , vol. 70, # 7 p. 2494 - 2502
反应条件
1.1: BuLi / tetrahydrofuran; hexane / 0.75 h / -75 °C
1.2: 92 percent / tetrahydrofuran; hexane
2.1: H2NNH2*H2O / tetrahydrofuran / 20 h / 50 °C
3.1: 6.41 g / tetrabutylammonium fluoride trihydrate / tetrahydrofuran / 2 h / 25 °C
4.1: 67 percent / CuSO4*5H2O / H2O / 0.75 h / Heating
5.1: 88 percent / H2O / 20 h / 50 °C
View Scheme
参考文献
Schlosser, Manfred; Bobbio, Carla; Rausis, Thierry
Journal of Organic Chemistry, 2005 , vol. 70, # 7 p. 2494 - 2502
反应条件
1.1: isobutylmagnesium chloride / tetrahydrofuran / 0.75 h / 0 °C
1.2: 94 percent / N-chlorosuccinimide / tetrahydrofuran / 0.75 h
2.1: BuLi / tetrahydrofuran; hexane / 0.75 h / -75 °C
2.2: 92 percent / tetrahydrofuran; hexane
3.1: H2NNH2*H2O / tetrahydrofuran / 20 h / 50 °C
4.1: 6.41 g / tetrabutylammonium fluoride trihydrate / tetrahydrofuran / 2 h / 25 °C
5.1: 67 percent / CuSO4*5H2O / H2O / 0.75 h / Heating
6.1: 88 percent / H2O / 20 h / 50 °C
View Scheme
参考文献
Schlosser, Manfred; Bobbio, Carla; Rausis, Thierry
Journal of Organic Chemistry, 2005 , vol. 70, # 7 p. 2494 - 2502
反应条件
1: 67 percent / CuSO4*5H2O / H2O / 0.75 h / Heating
2: 88 percent / H2O / 20 h / 50 °C
View Scheme
参考文献
Schlosser, Manfred; Bobbio, Carla; Rausis, Thierry
Journal of Organic Chemistry, 2005 , vol. 70, # 7 p. 2494 - 2502
反应条件
tris-(dibenzylideneacetone)dipalladium(0); 1,3-bis-(diphenylphosphino)propane; sodium t-butanolate in deuterated toluene
T=80°C; Buchwald-Hartwig Coupling; 36 h; Schlenk techniqueInert atmosphere;
参考文献
Isik, Murat; Tanyeli, Cihangir
Journal of Organic Chemistry, 2013 , vol. 78, # 4 p. 1604 - 1611