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高效的异对称合成西塔格利普丁的高度有效
Karl B Hansen1, Yi Hsiao, Feng Xu
1Department of Process Research, Merck Research Laboratory, Rahway, New Jersey 07065, USA.
Journal of the American Chemical Society
|June 11, 2009
概括
开发了一种新型的绿色合成方法,用于治疗2型糖尿病的西塔格利普丁. 这种高效的工艺可以产生高纯度的西塔利普丁酸盐,同时减少浪费和成本.
科学领域:
- 药用化学 医学化学
- 过程化学 过程化学
- 绿色化学 绿色化学
背景情况:
- 西塔格利普丁是一种选择性的二二基化酶-4 (DPP-4) 抑制剂.
- 它是治疗2型糖尿病 (T2DM) 的关键治疗剂.
- 现有的合成路线在效率和环境影响方面存在挑战.
研究的目的:
- 开发一种高效且环保的西塔利普丁合成方法.
- 为了优化脱水素利普丁中间体的制备.
- 为了在最后的化步骤中实现高的选择性.
主要方法:
- 一个一个,三步合成脱西塔利普丁中间体.
- 使用低负载的Rh (I) /Bu (t) JOSIPHOS催化剂进行高度选择性化.
- 将西塔利普丁分离为其酸盐.
主要成果:
- 脱西塔格利平的中间体是以82%的产量和>99.6%的重量%的纯度制备的.
- 西塔格利普丁几乎具有完美的光学和化学纯度.
- "绿色"合成可显著减少废物并消除水性废物流.
- 总体孤立产量达到了65%.
结论:
- 已经建立了一个具有成本效益,可扩展和环境可持续的西塔利普丁合成方法.
- 这种优化过程比以前的方法提供了实质性的改进.
- 开发的路线适合制造,并有助于更绿色的制药生产.
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