(1R,2R)-1-[(3,4-二甲氧基苯基)甲基]-2-[3-(叔丁氧基)-3-氧代丙基]-1,2,3,4-四氢-6,7-二甲氧基-2-甲基异喹啉苯磺酸盐合成路线 (共 4 条)
反应条件
1: (1R)-1-[(3,4-dimethoxyphenyl)-methyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-2-tert-butoxycarbonylethyl-isoquinoline oxalate With sodium hydroxide in water; toluene T=20°C; pH=9 - 10; 0.25 h; 2: benzenesulphonic acid methyl ester in acetonitrile T=30°C; 20 h;
参考文献
WO2008/132746 A1, ;
Page/Page column 34-36 ;
反应条件
1: (R)-N-(2-tert-butoxycarbonylethyl)-1,2,3,4-tetrahydropapaverine oxalate With sodium hydroxide in water pH=10; 2: benzenesulphonic acid methyl ester in acetonitrile T=30 - 35°C; 24 h;
参考文献
CHEMAGIS LTD.
Patent: WO2009/133556 A2, 2009 ;
Location in patent: Page/Page column 18; 19 ;
反应条件
trifluoroacetic acid T=0 - 5°C; 0.333333 h; Product distribution / selectivity;
参考文献
CHEMAGIS LTD.
Patent: WO2008/132748 A1, 2008 ;
Location in patent: Page/Page column 40 ;
反应条件
Na(1+)*HSO4(1-)*SiO2 = NaHSO4*SiO2 in dichloromethane 34 h; Heating / reflux; Product distribution / selectivity;
参考文献
CHEMAGIS LTD.
Patent: WO2009/7946 A1, 2009 ;
Location in patent: Page/Page column 17-18 ;