Haynes R K, Vonwiller S C
Department of Chemistry, Hong Kong University of Science and Technology, Kowloon.
Trans R Soc Trop Med Hyg. 1994 Jun;88 Suppl 1:S23-6. doi: 10.1016/0035-9203(94)90466-9.
The preparation of artemether from artemisinin is reviewed. Firstly, the extraction of artemisinin from Artemisia annua is described and an estimation of the yield per hectare based on literature data is given. Artemisinin is reduced with sodium borohydride to produce dihydroartemisinin as a mixture of epimers. The mixture is treated with methanol and an acid catalyst to provide artemether. Increasing demand for use of artemether places pressure on the supply of artemisinin, and an alternative means of preparing the drug from artemisinic acid, an abundant constituent of A. annua, which could triple current yields, is described. In anticipation of problems of drug resistance emerging with the continued use of artemether and artesunate to treat malaria, development of new derivatives of artemisinin which have enhanced stability is required. Examples of such derivatives which have been prepared in our laboratories, or proposed, are described.
本文综述了从青蒿素制备蒿甲醚的方法。首先,描述了从黄花蒿中提取青蒿素的过程,并根据文献数据估算了每公顷的产量。青蒿素用硼氢化钠还原生成二氢青蒿素,为差向异构体的混合物。该混合物用甲醇和酸催化剂处理得到蒿甲醚。蒿甲醚使用需求的增加给青蒿素的供应带来了压力,本文还描述了一种从黄花蒿的丰富成分青蒿酸制备该药物的替代方法,其产量可能会增加两倍。鉴于持续使用蒿甲醚和青蒿琥酯治疗疟疾会出现耐药性问题,需要开发稳定性更高的青蒿素新衍生物。本文介绍了我们实验室已制备或提出的此类衍生物的实例。