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乙二醇
甲醛
63148-62-9
MDI
丁酮
二甲基亚砜
碳酸氢钠
471-34-1
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乙二醇
甲醛
63148-62-9
MDI
丁酮
二甲基亚砜
碳酸氢钠
471-34-1
右维拉帕米
合成路线
(共 34 条)
3490-06-0
N-甲基-2-(3,4-二甲氧基苯基)乙胺
+
38176-01-1
→
反应条件
38321-02-7
右维拉帕米
反应条件
T=130°C; 1 h;
参考文献
Brenna, Elisabetta; Fuganti, Claudio; Grasselli, Piero; Serra, Stefano
European Journal of Organic Chemistry, 2001 , # 7 p. 1349 - 1357
54245-42-0
→
反应条件
38321-02-7
右维拉帕米
反应条件
aluminum oxide; potassium fluoride; potassium fluoride on basic alumina in acetonitrile T=100°C; 0.166667 h;
参考文献
Luurtsema, Gert; Windhorst, Albert D.; Mooijer, Martien P.J.; Herscheid, Jacobus D.M.; Lammertsma, Adriaan A.; Franssen, Eric J.F.
Journal of Labelled Compounds and Radiopharmaceuticals, 2002 , vol. 45, # 14 p. 1199 - 1207
67018-85-3
去甲维拉帕米
+
145577-00-0
→
反应条件
38321-02-7
右维拉帕米
反应条件
in acetonitrile T=50°C; 0.0833333 h;
参考文献
Luurtsema, Gert; Windhorst, Albert D.; Mooijer, Martien P.J.; Herscheid, Jacobus D.M.; Lammertsma, Adriaan A.; Franssen, Eric J.F.
Journal of Labelled Compounds and Radiopharmaceuticals, 2002 , vol. 45, # 14 p. 1199 - 1207
54245-42-0
+
67018-85-3
去甲维拉帕米
→
反应条件
38321-02-7
右维拉帕米
反应条件
in acetonitrile T=100°C; 0.0833333 h;
参考文献
Luurtsema, Gert; Windhorst, Albert D.; Mooijer, Martien P.J.; Herscheid, Jacobus D.M.; Lammertsma, Adriaan A.; Franssen, Eric J.F.
Journal of Labelled Compounds and Radiopharmaceuticals, 2002 , vol. 45, # 14 p. 1199 - 1207
36770-70-4
→
反应条件
38321-02-7
右维拉帕米
反应条件
1: 96 percent / triphenylphosphane / CCl4 / 2 h / Heating 2: 92 percent / 1 h / 130 °C View Scheme
参考文献
Brenna, Elisabetta; Fuganti, Claudio; Grasselli, Piero; Serra, Stefano
European Journal of Organic Chemistry, 2001 , # 7 p. 1349 - 1357
255721-21-2
→
反应条件
38321-02-7
右维拉帕米
反应条件
1: potassium hydroxide / methanol / 2 h / Heating 2: 96 percent / triphenylphosphane / CCl4 / 2 h / Heating 3: 92 percent / 1 h / 130 °C View Scheme
参考文献
Brenna, Elisabetta; Fuganti, Claudio; Grasselli, Piero; Serra, Stefano
European Journal of Organic Chemistry, 2001 , # 7 p. 1349 - 1357
349078-89-3
→
反应条件
38321-02-7
右维拉帕米
反应条件
1: 92 percent / pyridine 2: 85 percent / dimethylsulfoxide / 2 h / 80 °C 3: 81 percent / 20percent KOH / bis-(2-hydroxy-ethyl) ether / 1 h / Heating 4: 98 percent / diethyl ether 5: 84 percent / DIBAL-H / toluene / 1 h / 20 °C 6: 98 percent / pyridine 7: 68 percent / ozone; triphenylphosphane / CH2Cl2; methanol 8: hydroxylamine hydrochloride; sodium acetate / ethanol 9: 1.52 g / sodium acetate / acetic anhydride / Heating 10: potassium hydroxide / methanol / 2 h / Heating 11: 96 percent / triphenylphosphane / CCl4 / 2 h / Heating 12: 92 percent / 1 h / 130 °C View Scheme
参考文献
Brenna, Elisabetta; Fuganti, Claudio; Grasselli, Piero; Serra, Stefano
European Journal of Organic Chemistry, 2001 , # 7 p. 1349 - 1357
349078-90-6
→
反应条件
38321-02-7
右维拉帕米
反应条件
1: 90 percent / pyridine 2: 84 percent / dimethylsulfoxide / 2 h / 80 °C 3: 79 percent / 20percent KOH / bis-(2-hydroxy-ethyl) ether / 1 h / Heating 4: 97 percent / diethyl ether 5: 80 percent / DIBAL-H / toluene / 1 h / 20 °C 6: 98 percent / pyridine 7: 69 percent / ozone; triphenylphosphane / CH2Cl2; methanol 8: hydroxylamine hydrochloride; sodium acetate / ethanol 9: 1.19 g / sodium acetate / acetic anhydride / Heating 10: potassium hydroxide / methanol / 2 h / Heating 11: 96 percent / triphenylphosphane / CCl4 / 2 h / Heating 12: 92 percent / 1 h / 130 °C View Scheme
参考文献
Brenna, Elisabetta; Fuganti, Claudio; Grasselli, Piero; Serra, Stefano
European Journal of Organic Chemistry, 2001 , # 7 p. 1349 - 1357
349078-83-7
→
反应条件
38321-02-7
右维拉帕米
反应条件
1.1: lithium diisopropylamide / tetrahydrofuran / 0.08 h / -78 °C 1.2: trimethylchlorosilane / tetrahydrofuran / 3 h / Heating 1.3: methanol / 0.17 h / 20 °C 2.1: 97 percent / diethyl ether 3.1: 91 percent / DIBAL-H / toluene / 1 h / 20 °C 4.1: 90 percent / pyridine 5.1: 84 percent / dimethylsulfoxide / 2 h / 80 °C 6.1: 79 percent / 20percent KOH / bis-(2-hydroxy-ethyl) ether / 1 h / Heating 7.1: 97 percent / diethyl ether 8.1: 80 percent / DIBAL-H / toluene / 1 h / 20 °C 9.1: 98 percent / pyridine 10.1: 69 percent / ozone; triphenylphosphane / CH2Cl2; methanol 11.1: hydroxylamine hydrochloride; sodium acetate / ethanol 12.1: 1.19 g / sodium acetate / acetic anhydride / Heating 13.1: potassium hydroxide / methanol / 2 h / Heating 14.1: 96 percent / triphenylphosphane / CCl4 / 2 h / Heating 15.1: 92 percent / 1 h / 130 °C View Scheme
参考文献
Brenna, Elisabetta; Fuganti, Claudio; Grasselli, Piero; Serra, Stefano
European Journal of Organic Chemistry, 2001 , # 7 p. 1349 - 1357
349078-78-0
→
反应条件
38321-02-7
右维拉帕米
反应条件
1.1: lithium diisopropylamide / tetrahydrofuran / 0.08 h / -78 °C 1.2: trimethylchlorosilane / tetrahydrofuran / 3 h / Heating 1.3: 63 percent / methanol / 0.17 h / 20 °C 2.1: 97 percent / diethyl ether 3.1: 89 percent / DIBAL-H / toluene / 1 h / 20 °C 4.1: 92 percent / pyridine 5.1: 85 percent / dimethylsulfoxide / 2 h / 80 °C 6.1: 81 percent / 20percent KOH / bis-(2-hydroxy-ethyl) ether / 1 h / Heating 7.1: 98 percent / diethyl ether 8.1: 84 percent / DIBAL-H / toluene / 1 h / 20 °C 9.1: 98 percent / pyridine 10.1: 68 percent / ozone; triphenylphosphane / CH2Cl2; methanol 11.1: hydroxylamine hydrochloride; sodium acetate / ethanol 12.1: 1.52 g / sodium acetate / acetic anhydride / Heating 13.1: potassium hydroxide / methanol / 2 h / Heating 14.1: 96 percent / triphenylphosphane / CCl4 / 2 h / Heating 15.1: 92 percent / 1 h / 130 °C View Scheme
参考文献
Brenna, Elisabetta; Fuganti, Claudio; Grasselli, Piero; Serra, Stefano
European Journal of Organic Chemistry, 2001 , # 7 p. 1349 - 1357
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