3’,5’-O-(1,1,3,3-四异丙基-1,3-二硅氧烷)鸟苷合成路线 (共 2 条)
反应条件
1: DMSO, acetic anhydride 2: NaBH4 / 1.5 h / 0 °C 3: 80 percent / pyridine / 20 h / 60 °C 4: 80 percent / n-Bu4NF 5: 82 percent / p-toluenesulfonic acid / dioxane / 2 h / 23 °C 6: 78 percent / NaOH / acetonitrile; methanol; H2O 7: pyridine, (N,N-dimethylamino)pyrydine / CH2Cl2 / 1 h / 5 °C 8: tertbutylammonium fluoride / tetrahydrofuran / 5 h / 5 °C 9: 41 percent / Dowex 50W x 2-100 / methanol / 1 h / 23 °C 10: 80 percent / sat. NH3 in MeOH / 16 h / 20 °C View Scheme
参考文献
Kawasaki; Casper; Freier; Lesnik; Zounes; Cummins; Gonzalez; Cook
Journal of Medicinal Chemistry, 1993 , vol. 36, # 7 p. 831 - 841
反应条件
1: triethylamine; 4-dimethylaminopyridine / CH2Cl2 / 8 h / 20 °C 2: 2-tBuN-2-Et2N-1,3-dimethylperhydro-1,3,2-diazaphosphorine / acetonitrile / 1.5 h 3: tetrabutylammonium fluoride / tetrahydrofuran View Scheme
参考文献
Groetli, Morten; Douglas, Mark; Beijer, Barbro; Garcia, Ramon Gueimil; Eritja, Ramon; Sproat, Brian
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1997 , # 18 p. 2779 - 2788