目的:研究fagomine的最佳化学合成路线。方法:以3-氨基丙醇和1,3-二羟基丙酮为原料,通过Swern氧化、Aldol反应、还原胺化及催化氢化合成fagomine。结果:Fagomine经四步反应合成。产物结构经核磁共振、质谱确证。结论:以方便的四步反应合成了fagomine,产物将用于进一步的结构修饰。
Objective: To study the optimal synthetic route for fagomine. Method: The target compound was synthesized via multiple steps including Swem oxidation, Aldol reaction and reduced amination by applying 3-aminopmpyl alcohol and 1, 2-dihydroxyaeetone as starting materiaL. Results: Fagomine had been synthesized by four-step process. The structure was confirmed by nuclear magnetic resonance and eleetrospmy ionization mass spectrometry. Conclusion: Fourstep process has been developed for the synthesis of fagomine. The product will be used in the further structural modification.