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10-去乙酰基巴卡亭Ⅲ羟基保护反应过程的研究
Studies on the Protection of Hydroxy Groups in 10-deacetyl Baccatin III
【摘要】 对半合成紫杉醇类化合物的关键步骤 10-去乙酰基巴卡亭 Ⅲ(10-DAB)的羟基保护反应进行了研究。结果表明,利用氯甲酸(2,2,2-三氯)乙酯作为羟基保护基,获得7。10-二(三氯乙氧基)-10一去乙酰基巴卡亭Ⅲ[7,10-di(Troc)-10-DAB]的反应为连串反应,受反应时间和温度影响较大。当反应温度为 80℃,反应时间为 2 min时,目的产物 7,10-di(Troc)-10-DAB的反应选择性最好。
【Abstract】 The use of 2, 2, 2-trichloroethyl chloroformate as the hydroxy protecting group of 10deacetyl baccatinⅢ was studied to give 7, 10-di (2, 2, 2-trichloroethyloxycarbonyl)-10- baccatinⅢ, the key intermediate for the semisynthesis of taxanes. Result of the study showed that it is a consecutive reaction which could be significantly effected by reaction conditions of temperature and time. It was found that at 80C for 2 min the selectivity of 7, 10-di(2, 2, 2-trichloroethyloxycarbonyl)-10- baccatin Ⅲ is at its best.
【Key words】 10-deacetyl baccatin Ⅲ hydroxy group protection consecutive reaction 2; 2; 2trichloroethyl chloroformate;
- 【文献出处】 中草药 ,CHINESE TRADITIONAL AND HERBAL DRUGS , 编辑部邮箱 ,1999年10期
- 【分类号】R284
- 【被引频次】15
- 【下载频次】324