1-(4-氟苯基)-4-甲基戊-1,3-二酮合成路线 (共 12 条)
反应条件
hydrogenchloride in 1,4-dioxane
参考文献
Warner-Lambert Company
Patent: US4751229 A1, 1988 ;
反应条件
sodium hydride in 1,4-dioxane T=80 - 90°C; 4 h;
参考文献
Sliskovic; Roth; Wilson; Hoefle; Newton
Journal of Medicinal Chemistry, 1990 , vol. 33, # 1 p. 31 - 38
反应条件
1: potassium carbonate / acetone / 48 h / 20 °C / Inert atmosphere 2: potassium tert-butylate / tert-butyl alcohol / 24 h / 70 °C View Scheme
参考文献
Sterk, Damjan; Casar, Zdenko; Jukic, Marko; Kosmrlj, Janez
Tetrahedron, 2012 , vol. 68, # 9 p. 2155 - 2160
反应条件
1: potassium carbonate / acetone / 24 h / 20 °C 2: caesium carbonate / 2-methyl tetrahydrofuran / 10 h / 40 °C 3: triethylamine / dichloromethane / 8 h / -5 °C / Inert atmosphere 4: N-bromosuccinmide / acetonitrile / 0.5 h / UV-irradiation; Inert atmosphere; Sealed flow reactor View Scheme
参考文献
Sterk, Damjan; Casar, Zdenko; Jukic, Marko; Kosmrlj, Janez
Tetrahedron, 2012 , vol. 68, # 9 p. 2155 - 2160
反应条件
1: potassium carbonate / acetone / 24 h / 20 °C 2: caesium carbonate / 2-methyl tetrahydrofuran / 10 h / 40 °C 3: triethylamine / dichloromethane / 8 h / -5 °C / Inert atmosphere 4: N-bromosuccinmide / acetonitrile / 0.5 h / UV-irradiation; Inert atmosphere; Sealed flow reactor 5: sodium hydrogencarbonate; water / acetonitrile / 4 h / Reflux View Scheme
参考文献
Sterk, Damjan; Casar, Zdenko; Jukic, Marko; Kosmrlj, Janez
Tetrahedron, 2012 , vol. 68, # 9 p. 2155 - 2160
反应条件
1: potassium carbonate / acetone / 48 h / 20 °C / Inert atmosphere 2: potassium tert-butylate / tert-butyl alcohol / 24 h / 70 °C 3: triethylamine / dichloromethane / 8 h / -5 °C / Inert atmosphere 4: N-bromosuccinmide / acetonitrile / 16 h / 20 °C / Inert atmosphere; UV-irradiation 5: sodium hydrogencarbonate; dimethyl sulfoxide; sodium iodide / 71 h / 20 °C / Inert atmosphere View Scheme
参考文献
Sterk, Damjan; Casar, Zdenko; Jukic, Marko; Kosmrlj, Janez
Tetrahedron, 2012 , vol. 68, # 9 p. 2155 - 2160
反应条件
1: potassium carbonate / acetone / 24 h / 20 °C 2: caesium carbonate / 2-methyl tetrahydrofuran / 10 h / 40 °C 3: triethylamine / dichloromethane / 8 h / -5 °C / Inert atmosphere 4: N-bromosuccinmide / acetonitrile / 0.5 h / UV-irradiation; Inert atmosphere; Sealed flow reactor 5: sodium hydrogencarbonate; water / acetonitrile / 4 h / Reflux 6: acetic anhydride; dimethyl sulfoxide / 85 °C View Scheme
反应条件
1: potassium carbonate / acetone / 48 h / 20 °C / Inert atmosphere 2: potassium tert-butylate / tert-butyl alcohol / 24 h / 70 °C 3: triethylamine / dichloromethane / 8 h / -5 °C / Inert atmosphere 4: N-bromosuccinmide / acetonitrile / 16 h / 20 °C / Inert atmosphere; UV-irradiation 5: sodium hydrogencarbonate; dimethyl sulfoxide; sodium iodide / 71 h / 20 °C / Inert atmosphere View Scheme
参考文献
Tetrahedron, , vol. 68, # 9 p. 2155 - 2160
反应条件
1: potassium carbonate / acetone / 4.17 h / 20 °C
2: sodium hydride / tetrahydrofuran; mineral oil / 48 h / 25 °C
3: triethylamine / dichloromethane / 17 h / -5 °C / Inert atmosphere
4: Oxonereg;; sodium hydrogencarbonate / tetrabutyl-ammonium chloride / dichloromethane; water; acetone / 16 h / 0 - 20 °C
5: 1,4-diaza-bicyclo[2.2.2]octane / 1,4-dioxane / 24 h / 40 °C
6: acetic anhydride; dimethyl sulfoxide / 24 h / 20 °C
View Scheme
参考文献
LEK Pharmaceuticals d.d.
Patent: EP2423195 A1, 2012 ;
反应条件
hydrogenchloride in ethanol; isopropyl alcohol
40 h; Heating / reflux; Product distribution / selectivity;
参考文献
Butters, Michael; Lenger, Steven Robert; Murray, Paul Michael; Snape, Evan William
Patent: US2008/207903 A1, 2008 ;
Location in patent: Page/Page column 17 ;