知识与财富的链接
目的：合成高效、直接的FXa抑制剂利伐沙班。方法：以2-(2-氯乙氧基)乙酰氯、对硝基苯胺为原料,合成利伐沙班。结果：合成了利伐沙班,总收率为42.46%,纯度95.19%(HPLC)。结论：通过优化反应条件,缩短了反应时间。
Objective: To synthesize the effective and direct FXa inhibitor, rivaroxaban. Methods: Rivaroxaban was synthesized by 2-(2-chloro-ethoxy) chloride and p-nitroaniline. Results: Rivaroxaban was synthesized with a total yield of 42.46%. The purity of rivaroxaban was 95.19% (HPLC). Conclusion: The reaction time is decreased by optimizing the reaction conditions.
