期刊文献+

新型含1,2,3-三唑基[1,2,4]噁二唑并[4,5-a][1,5]苯并硫氮杂卓化合物的合成 被引量:3

Synthesis of 2-Phenyl-1,2,3-triazol-4-yl[1,2,4] Oxadiazolo[4,5-a][1,5] benzothiazepine Derivatives
下载PDF
导出
摘要 将1,2,3-三唑环结构及1,2,4-噁二唑环等多个药效团结构叠加到同一个硫氮杂卓分子中,为药理及生理活性研究提供较好的先导化合物。反应在三乙胺存在下,用2,4-二芳基-2,3-二氢-1,5-苯并硫氮杂卓与α-氯代-2-苯基-1,2,3-三唑基-4-甲醛肟在室温进行1,3-偶极环加成反应,合成一系列的2-苯基-1,2,3-三唑基[1,2,4]噁二唑并[4,5-a][1,5]苯并硫氮杂卓化合物,并采用红外光谱、核磁共振、元素分析等测试技术对化合物进行了表征。 In the presence of triethylamine, the reaction of 2,4-disubstituted-2,3-dihydro-1, 5-benzothiazepine with α-chloro-2-phenyl-1,2,3-triazole-4-carbaldehyde oxime through 1,3-dipolar cyeloadditon produces a series of 2-phenyl-1,2,3-triazol-4-yl [ 1,2,4 ] oxadiazolo [ 4,5-a ] [ 1,5 ] benzothiazepine derivatives. The compounds bearing benzothiazepine, 1,2,3-triazole and 1,2,4-oxadiazole moieties may possess interesting bioactivities.
出处 《应用化学》 CAS CSCD 北大核心 2008年第12期1389-1392,共4页 Chinese Journal of Applied Chemistry
基金 国家自然科学基金(20562011) 新疆大学青年启动基金资助项目
关键词 环加成反应 苯并硫氮杂卓 合成 cycloadditon reaction, oxime, benzothiazepine, synthesis
  • 相关文献

参考文献15

  • 1Weiss K, Fitscha P, Gazso A. Chem Abstr[ J ], 1959,111:70 642
  • 2Etingin O R, Hajjar D P. Chem Abstr[ J ], 1990,112:91 510
  • 3Kirsanova G Y,Tsorin I B,Chickanov G. Chem Abstr[J] ,1989,111:33 372
  • 4Takeda M,Oishi A,Nakajina H. Chem Abstr[J] ,1986,105:183 965
  • 5Mogilnika E, Czyark A, Maj J. Eur J Pharmacol[ J ], 1987,138:413
  • 6Jadhav K P, Ingle D B. Indian J Chem Sect B[ J] , 1983,22B : 180
  • 7Corral C,Lissavetzky J,Valdolmillos A M. J Heterocyclic Chem[J], 1985,22:1 349
  • 8Bunin B A,Ellman J A. J Am Chem Soc[J] ,1992,114:10 997
  • 9ZHAO Yan-Lai(赵雁来),HE Sen-Quan(何森泉),XU Chang-De(徐长得).Heterocyclic Chemistry Introduction(杂环化学导论)[M].Beijing(北京):Higher Education Press(高等教育出版社),1992
  • 10刘方明,于建新,鲁文杰,刘罡,刘育亭,陈耀祖.3-取代胺甲基-5-连三唑基-1,3,4-噁二唑-2-硫酮的合成[J].有机化学,1999,19(2):157-161. 被引量:4

二级参考文献10

共引文献44

同被引文献21

  • 1赵海燕,刘刚.苯并硫氮杂类化合物的研究进展[J].中国药物化学杂志,2007,17(2):122-128. 被引量:1
  • 2郑虎.药物化学(第4版)[M].北京:人民卫生出版社,2001.
  • 3郑虎.药物化学[M].4版.北京:人民卫生出版社,2001:140.
  • 4Sampath K H M,Chakravarthy P P,Rao M S,et al.Solid phase synthesis of hydroxy benzothiazepinones through cyclative release under thermolysis[J].Chem Lett,2004,33(7):888-889.
  • 5Sashida H,Satoh H.Studies on tellurium-containing heterocycles.part 22.tellurazepine ring system:preparation of 1,5-benzotellurazepin-4-ones and their conversion into fully unsaturated l,5-benzotellurazepines[J].Chem Pharm Bui,2004,52(4):413-417.
  • 6Morton G C,Salvino J M,Labaudiniere R F,et al.Novel solid-phase synthesis of 1,5-benzothiazepine-4-one derivatives[J].Tetrahedron Lett,2000,41(17):3029-3033.
  • 7Batsanov A S,Collings J C,Fairlamb I J S,et al.Requirement for an oxidant in Pd/Cu co-catalyzed terminal alkyne homocoupling to give symmetrical 1,4-disubstituted 1,3-diynes[J].J Org Chem 2005,70(2):703-706.
  • 8Li J H,Liang Y,Zhang X D.Amine-and phosphine-free palladium(ⅱ)-catalyzed homocoupling reaction of terminal alkynes[J].Tetrahedron,2005,61(7):1903-1907.
  • 9Li J H,Liang Y,Wang D P,et al.Efficient stille cross-coupling reaction catalyzed by the pd(oac)2/dabco catalytic system[J].J Org Chem,2005,70(7):2832-2834.
  • 10Li J H,Liu W J.Dabco as an inexpensive and highly efficient ligand for palladium-catalyzed Suzuki-Miyaura cross-coupling reaction[J].Org Lett,2004,6(16):2809-2811.

引证文献3

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