55094-52-5

基本信息
1号中间体
伦德西韦杂质4
瑞德西韦杂质21
瑞德西韦中间体I
瑞德西韦1号中间体
2,3,5-三苄氧基-D-核糖酸-1
2,3,5-三苄氧基-D-核糖酸-1,4-内
2,3,5-三苄氧基-D-核糖酸-1,4-内酯
2,3,5-三-O-苄基-D-核糖酸-Γ-内酯
JACS-55094-52-5
2,3,5-TRI-O-BENZYL-D-RIBONOLACTONE
2,3,5-Tri-O-benzyl-D-ribono-1,4-lactone
2,2,5-tri-O-benzyl-D-ribono-1,4-lancton
2,3,5-Tri-O-benzyl-D-ribonic Acid 1,4-lactone
2,3,5-Tris-O-(phenylmethyl)-D-ribonic acid γ-lactone
D-Ribonic acid, 2,3,5-tris-O-(phenylmethyl)-, γ-lactone
1, 4-lactone, 2,3, 5-tribenzoxy-D-ribosate-1, 4-lactone
1-Chloro-3,5-di-(p-chlorobenzoyl)-2-deoxy-D-ribofuranose
物理化学性质
制备方法

16838-89-4

14233-64-8
以2,3,5-三-O-(苯基甲基)-D-呋喃核糖为原料合成2,3,5-三苄氧基-D-阿拉伯糖酸-1,4-内酯的一般步骤:将化合物30a(根据J. Org. Chem., 1961, 26, 4605制备;10.0 g,23.8 mmol)溶解于无水DMSO(30 mL)中,并在氮气保护下搅拌。随后加入乙酸酐(20 mL),反应混合物在室温下持续搅拌48小时。通过LC/MS监测反应完成后,将反应混合物缓慢倒入冰水(500 mL)中,继续搅拌20分钟。用乙酸乙酯(3×200 mL)萃取水相,合并有机相后用去离子水(3×200 mL)洗涤。弃去水相,有机相经无水MgSO4干燥后减压浓缩至干。将残余物溶解于二氯甲烷(DCM)中,并通过硅胶柱色谱法进行纯化,使用25%乙酸乙酯/己烷作为洗脱剂,得到目标产物30b,收率为96%。1H-NMR(CD3CN)数据:δ 3.63-3.75(m,2H),4.27(d,1H),4.50-4.57(m,3H),4.65(s,3H),4.69-4.80(m,2H),7.25(d,2H),7.39(m,13H)。
参考文献:
[1] Patent: WO2010/93608, 2010, A1. Location in patent: Page/Page column 158
[2] Patent: WO2011/35250, 2011, A1. Location in patent: Page/Page column 70-71
[3] Patent: WO2012/12776, 2012, A1. Location in patent: Page/Page column 109
[4] Patent: US2017/71964, 2017, A1. Location in patent: Paragraph 0517-0518
[5] Journal of Carbohydrate Chemistry, 2008, vol. 27, # 5, p. 332 - 344
报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
2025/05/22 | 46864 | 2,3,5-三-O-苯甲基-D-核酮-1,4-内酯 2,3,5-Tri-O-benzyl-D-ribono-1,4-lactone, Thermo Scientific Chemicals | 55094-52-5 | 1g | 514元 |
2025/05/22 | 46864 | 2,3,5-三-O-苯甲基-D-核酮-1,4-内酯 2,3,5-Tri-O-benzyl-D-ribono-1,4-lactone, Thermo Scientific Chemicals | 55094-52-5 | 5g | 1548元 |
2025/05/22 | T3955 | 2,3,5-三-O-苄基-D-核糖酸-1,4-内酯 2,3,5-Tri-O-benzyl-D-ribono-1,4-lactone | 55094-52-5 | 5G | 150元 |