期刊文献+

基于室温条件及无金属催化的多组分反应构建4-氨基-2-烷基-6-苯基-5-腈基嘧啶分子骨架

The Room-Temperature Metal-Free Muticomponent Synthesis of 4-Amino-2-Alkylsulfanyl-6-Aryl-5-Cyanopyrimidines
下载PDF
导出
摘要 以硫脲、苯甲醛、丙二腈和溴代脂肪烃为原料,在无金属催化及室温条件下,建立了可以较高产率制备4-氨基-2-烷基-6-苯基-5-腈基嘧啶等嘧啶环系列化合物的4组分合成新方法,所得的合成新方法具有良好的普适性以及进一步推广应用的潜力. New four-component tandem reactions of malononitrile,halohydrocarbon,thiourea and aromatic aldehyde have been successfully developed only at room temperature and under metal-free conditions,in good to excellent yields of 4-amino-6-aryl-5-cyanopyrimidines.
出处 《江西师范大学学报(自然科学版)》 CAS 北大核心 2016年第2期174-178,共5页 Journal of Jiangxi Normal University(Natural Science Edition)
基金 国家自然科学基金(21262018)资助项目
关键词 多组分反应 室温 无金属 嘧啶 multicomponent reactions room temperature metal-free pyrimidine
  • 相关文献

参考文献15

  • 1Bkojgude S S, Biju D A. Arynes in transition-metal-fFeemidticomponent coupling reactions [ J ] . Angewandte Che-mie International Edition,2012,51(7) : 1520-1522.
  • 2Alexander D,Wang Wei,Wang Kan. Chemistry and biolo-gy of multicomponet reactions [ J ]. Chemical Reviews,2012,112(6)-.3083-3135.
  • 3Junichiro Y, Atsushi D. C-H bood functionalization:emer-ging synthetic tools for natural products and pharmaceuti-cals [J]. Angewandte Chemie International Edition,2012,51(36);8960-9009.
  • 4Beingessner R L’Deng B-L, Fan wick P E,et al. A regiose-lective approach to trisubstituted 2 (or 6)-arylaminopyri-midine-5 -carbaldehydes and their application in the syn-thesis of structurally and electronically unique G 八 C baseprecursors [J]. J Org Chem,2008,73(3) :931-939.
  • 5Payton M,Geuns-Meyer S D. Discovery of a potent,selec-tive ,and orally bioavailable pyridinyl-pyrimidine phthala-zine aurora kinase inhibitor [ J]. J Med Chem,2010,53(17):6368-6377.
  • 6Mukhopadhyay C’Das P,Butcher R J. An expeditious andefficient synthesis of highly functionalized [ 1,6] -naphthy-ridine8 under catalyst-free conditions in aqueous medium[J]. Org Lett,2011,13 (17) :46644667.
  • 7Danel K, Pedersen E B, Nielsen C_ Synthesis and anti-HIV-1 activity of novel 2,3-dihydro-7ff-thiazolo [ 3,2-a ]pyrimidin-7-ones f J ]. J Med Chem, 1998,41 (2) : 191-198.
  • 8Horvath A, Vasvari-Debreczy L, Dessy F,et al. Nitrogenbridgehead compounds. Part 18. New antiallergic 4H-pyri-do[ 1,2-o ] pyrimidin-4-ones. Part I [ J ]. J Med Chem,1982,25(10)-.1140-1145.
  • 9Bennett L R,Blankley C J,Fleming R W. Antihypertensiveactivity of 6-arylpyrido [ 2,3 ] pyrimidin-7 -amine deriva-tives [J].J Med Chem,1981,24(4) :382-389.
  • 10Blankley C J,Bennett L R,Fleming R W,et al. Antihyper-tensive activity of 6-arylpyridof 2,3-^] pyrimidin-7-aminederivatives. 2,7-Acyl amide analogs [ J]. J Med Chem,1983,25(3):403^11.

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