期刊文献+

用IBX对醋酸去氢表雄酮选择性脱氢合成3β-乙酰氧基-雄甾-Δ^(5,15)-二烯-17-酮 被引量:2

Synthesis of 3β-Acetoxy-androstan-Δ^(5,15)-dien-17-one from IBX Selective Dehydrogen of Dehydroepiandrosterone Acetate
下载PDF
导出
摘要 以醋酸去氢表雄酮为起始原料,于温度为65~70℃的DMSO-甲苯混合溶剂中,反应时间为22h,利用二碘酰基苯甲酸(IBX)对醋酸去氢表雄酮的选择性脱氢简便高效地合成了曲螺酮关键中间体3β-乙酰氧基-雄甾-Δ5,15-二烯-17-酮;探讨了IBX与醋酸去氢表雄酮的摩尔比对目标化合物的收率影响。实验表明,在n(IBX)∶n(醋酸去氢表雄酮)=1.5∶1.0时,目标化合物的收率最佳,达到73%。目标化合物经紫外光谱、红外光谱、核磁共振氢谱、质谱及元素分析测试技术确证了其化学结构。 3β-Acetoxy-androstan-△^5,15-dien-17-one was conveniently and effectively synthesized from IBX selective dehydrogen of dehydroepiandrosterone acetate in DMSO-toluene at 65 - 70 ℃ for 22 h, and the effect of the molar ratio of IBX to dehydroepiandrosterone on the yield of target product was probed, indicating that the weight yield was optimal up to 73% when the molar ratio of IBX to dehydroepiandrosterone was 1.5. The chemical structure of target product was characterized by UV, IR,^1 H NMR, MS, and elemental analysis.
出处 《应用化学》 CAS CSCD 北大核心 2008年第8期992-994,共3页 Chinese Journal of Applied Chemistry
关键词 醋酸去氢表雄酮 IBX β-乙酰氧基-雄甾-△^5 15-二烯-酮 α β-不饱和羰基甾体 中间体 dehydroepiandrosterone acetate, IBX β-acetoxy-androstan-△^5,15 -dien-one, α, β-unsaturated carbonyl steroid, intermediates
  • 相关文献

参考文献10

二级参考文献189

  • 1宋发军.甾体药物源植物薯蓣属植物中薯蓣皂甙元的研究及生产状况[J].天然产物研究与开发,2002,14(3):89-93. 被引量:54
  • 2法幼华 徐诗伟 等.利用剑麻皂素合成大力补[J].医药工业,1980,(6):9-11.
  • 3Weber A, Kennecke M. Process for the preparation of 3-oxodelta- 1,4- steroids [ P]. EP: 54810,1989-06-13.
  • 4Charles M,Albert W. Process for the manufacture of 1-dehydro- 17- alpha- methyl- testosterone [ P ]. US: 3366649,1968-01 -30.
  • 5Burn D, Oliver W G, Neville K D, et al. Process for the preparation of 3-oxo-and 3-oxo-steroids [ P ]. GB: 854343,1960-11-16.
  • 6Zhdankin V V,Stang P J. Recent developments in the chemistry of polyvalent iodine compounds[J]. Chem. Rev. ,2002,102(7) :2523-2584.
  • 7Stang P J, Zhdankin V V. Organic polyvalent iodine compounds[J]. Chem. Rev. ,1996,96(3) :1123-1178.
  • 8Wirth T, Hirt U H. Hypervalent iodine compounds: Recent advances in synthetic applications[J]. Synthesis, 1999:1271-1287.
  • 9Mulbaier M, Giannis A. The synthesis and oxidative properties of polymer-supported IBX [ J ]. Angew. Chem. , Int. Ed.,2001,40(23) :4393-4400.
  • 10Paintner F F, Allmendinger L, Bauschke G. Highly regioselective 3-hydroxyalkylations of boron 4-methoxy-2-furanolates: A new entry to 5-unsubstituted and 5-monsubstituted 3-acyl-4-o-methyl tetronates [ J ]. Synthesis, 2001: 2113-2118.

共引文献26

同被引文献20

引证文献2

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部