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乙二醇
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63148-62-9
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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
盐酸普拉克索
合成路线
(共 10 条)
943319-02-6
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反应条件
104632-25-9
盐酸普拉克索
反应条件
acetyl chloride in isopropyl alcohol T=5 - 20°C; 12.5 h;
参考文献
INSTYTUT FARMACEUTYCZNY
Patent: WO2007/75095 A1, 2007 ;
Location in patent: Page/Page column 7 ;
106006-84-2
s-2-氨基-6-丙酰氨基-4,5,6,7-四氢苯并噻唑
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反应条件
104632-25-9
盐酸普拉克索
反应条件
1: With chloro-trimethyl-silane in dichloromethane T=0 - 15°C; Inert atmosphere; 2: With lithium aluminium tetrahydride in tetrahydrofuran; dichloromethane T=-10 - 0°C; Inert atmosphere;
参考文献
Ravinder; Rajeswar Reddy; Panasa Reddy; Bandichhor, Rakeshwar
Tetrahedron Letters, 2013 , vol. 54, # 36 p. 4908 - 4913
104632-26-0
盐酸普拉克索
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反应条件
104632-25-9
盐酸普拉克索
反应条件
hydrogenchloride in water; acetone T=0 - 3°C; pH=1.5; 2 h; Product distribution / selectivity;
参考文献
Helm AG; CF Pharma Gyogyszergyarto Kft.
Patent: EP1878731 A1, 2008 ;
Location in patent: Page/Page column 11 ;
1001648-71-0
(6S,7S)-2-氨基-4,5,6,7-四氢-6-(丙基氨基)-7-苯并噻唑醇
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反应条件
104632-25-9
盐酸普拉克索
反应条件
1: With hydrogenchloride; formic acid in water 2: With hydrogen; palladium on activated carbon in water Product distribution / selectivity;
参考文献
Helm AG; CF Pharma Gyogyszergyarto Kft.
Patent: EP1878731 A1, 2008 ;
Location in patent: Page/Page column 11 ;
106006-83-1
2,6-二氨基-4,5,6,7-四氢苯并噻唑
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反应条件
104632-25-9
盐酸普拉克索
反应条件
1.1: water / 70 °C / Reflux; Resolution of racemate 2.1: hydrogenchloride / water / carbon treatment 2.2: 1.5 h / 25 - 30 °C 3.1: triethylamine / methanol / 1.5 h / 10 - 20 °C 4.1: sodium tetrahydroborate; boron trifluoride diethyl etherate / tetrahydrofuran / 4 h / 0 - 50 °C 4.2: 0.17 h / 10 °C 5.1: hydrogenchloride / water; methanol / 0.75 h / 25 - 30 °C View Scheme
参考文献
WO2011/21214 A2, ;
104617-50-7
N-(2-氨基-4,5,6,7-四氢-6-苯并噻唑基)乙酰胺单氢溴酸盐
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反应条件
104632-25-9
盐酸普拉克索
反应条件
1.1: water; sulfuric acid / 10 h / Reflux 1.2: 1.5 h / 0 - 30 °C 2.1: water / 70 °C / Reflux; Resolution of racemate 3.1: hydrogenchloride / water / carbon treatment 3.2: 1.5 h / 25 - 30 °C 4.1: triethylamine / methanol / 1.5 h / 10 - 20 °C 5.1: sodium tetrahydroborate; boron trifluoride diethyl etherate / tetrahydrofuran / 4 h / 0 - 50 °C 5.2: 0.17 h / 10 °C 6.1: hydrogenchloride / water; methanol / 0.75 h / 25 - 30 °C View Scheme
参考文献
WO2011/21214 A2, ;
27514-08-5
4-乙酰氨基环己酮
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反应条件
104632-25-9
盐酸普拉克索
反应条件
1.1: bromine; acetic acid / 0.75 h / 25 - 35 °C 1.2: 3 h / Reflux 2.1: water; sulfuric acid / 10 h / Reflux 2.2: 1.5 h / 0 - 30 °C 3.1: water / 70 °C / Reflux; Resolution of racemate 4.1: hydrogenchloride / water / carbon treatment 4.2: 1.5 h / 25 - 30 °C 5.1: triethylamine / methanol / 1.5 h / 10 - 20 °C 6.1: sodium tetrahydroborate; boron trifluoride diethyl etherate / tetrahydrofuran / 4 h / 0 - 50 °C 6.2: 0.17 h / 10 °C 7.1: hydrogenchloride / water; methanol / 0.75 h / 25 - 30 °C View Scheme
参考文献
WO2011/21214 A2, ;
106092-09-5
(S)-2,6-二氨基-4,5,6,7-四氢苯并噻唑
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反应条件
104632-25-9
盐酸普拉克索
反应条件
1.1: triethylamine / methanol / 1.5 h / 10 - 20 °C 2.1: sodium tetrahydroborate; boron trifluoride diethyl etherate / tetrahydrofuran / 4 h / 0 - 50 °C 2.2: 0.17 h / 10 °C 3.1: hydrogenchloride / water; methanol / 0.75 h / 25 - 30 °C View Scheme
参考文献
WO2011/21214 A2, ;
873431-80-2
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反应条件
104632-25-9
盐酸普拉克索
反应条件
1.1: hydrogenchloride / water / carbon treatment 1.2: 1.5 h / 25 - 30 °C 2.1: triethylamine / methanol / 1.5 h / 10 - 20 °C 3.1: sodium tetrahydroborate; boron trifluoride diethyl etherate / tetrahydrofuran / 4 h / 0 - 50 °C 3.2: 0.17 h / 10 °C 4.1: hydrogenchloride / water; methanol / 0.75 h / 25 - 30 °C View Scheme
参考文献
WO2011/21214 A2, ;
104632-25-9
盐酸普拉克索
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反应条件
104632-26-0
盐酸普拉克索
反应条件
potassium hydroxide in water T=20°C; 1 - 2 h; Product distribution / selectivity;
参考文献
Gribun, Irina; Salman, Ada; Shiffer, Meital; Shookrun, Moty; Brand, Michael; Arad, Oded; Kaspi, Joseph
Patent: US2006/69263 A1, 2006 ;
Location in patent: Page/Page column 4 ;