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新型抗艾滋病药物地拉韦啶的合成
Synthesis of a New Anti-aids Drug Delavirdine Mesylate
【摘要】 以烟酰胺、对硝基苯肼、丙酮酸乙酯等为原料,N,N-羰基二咪唑(CD I)为缩合剂合成地拉韦啶甲磺酸盐.合成总收率为6.6%.关键中间体及地拉韦啶甲磺酸盐的结构经红外光谱、核磁共振氢谱及碳谱、质谱、元素分析等得到确证.
【Abstract】 Delavirdine mesylate was synthesized with CDI acting as condensation agent from the reaction of nicotinamide,p-nitrophenylhydrazine and ethyl pyruvate. Delavirdine mesylate was obtained at a total yield of 6.6%.The structures of the target molecule and the key intermediates were confirmed by IR,()1H NMR,(()13C NMR,) MS,and element analysis.
【关键词】 合成;
地拉韦啶;
药物化学;
抗艾滋病药物;
【Key words】 synthesis; delavirdine; medicinal chemistry; anti-HIV-1 drug;
【Key words】 synthesis; delavirdine; medicinal chemistry; anti-HIV-1 drug;
【基金】 吉林大学创新基金(批准号:2003CX063)
- 【文献出处】 吉林大学学报(理学版) ,Journal of Jilin University(Science Edition) , 编辑部邮箱 ,2006年01期
- 【分类号】R914
- 【被引频次】11
- 【下载频次】629