375854-77-6
375854-77-6 结构式
基本信息
2-(trimethylsilyl)ethyl 1,2,3,6-tetrahydro-4-trifluoromethylsulfonyloxy-pyridine-1-carboxylate
2-(Trimethylsilyl)ethyl 4-(((trifluoromethyl)sulfon-yl)oxy)-5,6-dihydropyridine-1(2H)-carboxyl
1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-4-[[(trifluoromethyl)sulfonyl]oxy]-, 2-(trimethylsilyl)ethyl ester
制备方法
181701-30-4
37595-74-7
375854-77-6
在氮气氛围下,将1M的双(三甲基硅基)氨基锂/THF溶液(485mL)用干燥的四氢呋喃(1L)稀释,并将溶液冷却至-78℃。在55分钟内,向搅拌的溶液中逐滴加入4-氧代哌啶-1-羧酸2-(三甲基硅烷基)乙酯(106g,436mmol)的无水四氢呋喃(400mL + 75mL冲洗液)溶液。45分钟后,在45分钟内滴加N-苯基双(三氟甲烷磺酰)亚胺(158.8g,445mmol)的无水四氢呋喃(700mL + 50mL冲洗液)溶液。在-78℃下反应1小时后,将反应混合物转移至冰浴中继续反应3小时,随后进行真空浓缩。将残余物用水稀释,水层用乙醚/环己烷(1:1)混合溶剂萃取两次。合并有机层,用无水硫酸镁干燥,并在冰箱中静置过夜。真空浓缩后,得到158.6g(产率97%)的2-(三甲基甲硅烷基)乙基4-(((三氟甲基)磺酰)氧基)-5,6-二氢吡啶-1(2H)-羧酸叔丁酯,产物为琥珀色油状物。1H NMR(CDCl3)δ5.78(宽单峰,1H),4.21(多重峰,2H),4.10(多重峰,2H),3.68(三重峰,2H,J = 5.3Hz),2.46(多重峰,2H),1.02(多重峰,2H),0.05(单峰,9H)。
参考文献:
[1] Patent: WO2004/60884, 2004, A1. Location in patent: Page 23-24
[2] Bioorganic and Medicinal Chemistry, 2005, vol. 13, # 8, p. 2859 - 2872
[3] Patent: WO2004/60884, 2004, A1. Location in patent: Page 19-20
[4] Patent: WO2011/79102, 2011, A1. Location in patent: Page/Page column 26-27
[5] Patent: WO2011/78984, 2011, A1. Location in patent: Page/Page column 27