benzyl N-[3-[[(3aR,4R,6R,6aR)-4-(6-aminopurin-9-yl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-6-yl]methyl-methylamino]-2-methylpropyl]carbamate 在
20% palladium hydroxide-activated charcoal
氢气 、
三乙胺 作用下,
以
甲醇 、
二氯甲烷 为溶剂,
20.0 ℃
、101.33 kPa
条件下,
生成 1-[3-[[(3aR,4R,6R,6aR)-4-(6-aminopurin-9-yl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-6-yl]methyl-methylamino]-2-methylpropyl]-3-(4-tert-butylphenyl)urea