摘要
目的:合成抗肿瘤新药脱水长春碱。方法:以长春质碱和文多灵为原料经2步反应合成脱水长春碱。结果:脱水长春碱结晶物收率为34.29%,目标产物经紫外光谱、红外光谱、质谱、核磁共振氢谱得到确证。结论:新的合成方法工艺简单,操作安全,适合生产。
Objective: To synthesize an anti-tumor agent anhydrovinblastine. Methods: The target compound was synthesized via two steps from catharanthine and vindoline as starting materials. Results: A total yield of 34.29% was obtained and the chemical structure of the target compound was confirmed by UV, IR, MS and ^1H-NMR. Conclusion: The easily manipulated new synthetic procedure is worthy to have further pilot manufacture.
出处
《中国新药杂志》
CAS
CSCD
北大核心
2006年第13期1087-1089,共3页
Chinese Journal of New Drugs