(顺式)-1,3-二苄基二氢-1H-呋喃并[3,4-d]咪唑-2,4,6(3H)-三酮合成路线 (共 9 条)
反应条件
in toluene 10 h; Reflux;
参考文献
Xiong, Fei; Chen, Xu-Xiang; Chen, Fen-Er
Tetrahedron Asymmetry, 2010 , vol. 21, # 6 p. 665 - 669
反应条件
1: 84 percent / conc. HCl / dioxane / 2.5 h / Ambient temperature 2: 2) 6.25percent aq. HCl / 1) acetone, water 3: 1) AgNO3, 1N NaOH, 2) Ac2O / 1) H2O, EtOH, r.t., 2) reflux, 5 min View Scheme
参考文献
Senuma; Fujii; Seto; Okamura; Date; Kinumaki
Chemical and Pharmaceutical Bulletin, 1990 , vol. 38, # 4 p. 882 - 887
反应条件
sodium hydroxide; acetic anhydride; silver nitrate 1) H2O, EtOH, r.t., 2) reflux, 5 min; Yield given. Multistep reaction;
参考文献
Senuma; Fujii; Seto; Okamura; Date; Kinumaki
Chemical and Pharmaceutical Bulletin, 1990 , vol. 38, # 4 p. 882 - 887
反应条件
1: 2) 6.25percent aq. HCl / 1) acetone, water 2: 1) AgNO3, 1N NaOH, 2) Ac2O / 1) H2O, EtOH, r.t., 2) reflux, 5 min View Scheme
参考文献
Senuma; Fujii; Seto; Okamura; Date; Kinumaki
Chemical and Pharmaceutical Bulletin, 1990 , vol. 38, # 4 p. 882 - 887
参考文献
Hoffmann-La Roche
Patent: US2489232 , 1946 ;
Full Text Show Details
Hoffmann-La Roche
Patent: DE820309 , 1951 ;
DRP/DRBP Org.Chem.
反应条件
sodium sulfide in tetrahydrofuran T=20°C; Substitution; 3 h;
参考文献
Chen; Huang; Fu; Cheng; Zhang; Li; Peng
Synthesis, 2000 , # 14 p. 2004 - 2008
反应条件
potassium tert-butylate; hydrogen in toluene T=25°C; P=76005.1 Torr; 12 h; Autoclave; optical yield given as percent eeenantioselective reaction;
参考文献
Yoshimura, Masahiro; Tsuda, Kazuomi; Nakatsuka, Hiroshi; Yamamura, Tomoya; Kitamura, Masato
Tetrahedron, 2011 , vol. 67, # 51 p. 10006 - 10010
反应条件
[Ru(II)(η6-benzene)(μ-Cl)Cl]2; C33H48OP2; potassium tert-butylate; hydrogen in toluene T=110°C; P=76005.1 Torr; 32 h; Autoclave; optical yield given as percent eeenantioselective reaction;
参考文献
Yoshimura, Masahiro; Tsuda, Kazuomi; Nakatsuka, Hiroshi; Yamamura, Tomoya; Kitamura, Masato
Tetrahedron, 2011 , vol. 67, # 51 p. 10006 - 10010
反应条件
1.1: 3-(3,5-bis-trifluoromethyl-phenylamino)-4-{[(S)-(6-methoxy-quinolin-4-yl)-((R)-5-vinyl-1-aza-bicyclo[2.2.2]oct-2-yl)-methyl]-amino}-cyclobut-3-ene-1,2-dione / tert-butyl methyl ether / 24 h / 25 °C / Inert atmosphere 2.1: calcium chloride / ethanol / 0 - 25 °C / Inert atmosphere 3.1: hydrogenchloride / water / 0.5 h / 55 °C / Inert atmosphere 4.1: PhCOSK / N,N-dimethyl-formamide / 2 h / 150 °C / Inert atmosphere 5.1: iodine; magnesium / tetrahydrofuran / 1 h / Inert atmosphere; Reflux 5.2: 2 h / Reflux; Inert atmosphere 5.3: 3 h / Reflux 6.1: palladium 10 on activated carbon; hydrogen / isopropyl alcohol / 12 h / 110 °C / 45603.1 Torr 7.1: hydrogenchloride; formic acid / water / 5 h / Reflux; Inert atmosphere 8.1: dimethyl sulfoxide / 3 h / 90 °C / Inert atmosphere 9.1: water; hydrogen bromide / 10 h / Reflux; Inert atmosphere View Scheme
参考文献
Xiong, Fei; Xiong, Fang-Jun; Chen, Wen-Xue; Jia, Hui-Qing; Chen, Fen-Er
Journal of Heterocyclic Chemistry, 2013 , vol. 50, # 5 p. 1078 - 1082