期刊文献+

1-苄基-4-(4-甲氧基)-苯基-1,2,3-三唑的合成 被引量:1

Preparation of 1-Benzyl-4-(4-Methyloxy)Phenyl-1, 2, 3-Triazole
下载PDF
导出
摘要 采用氯苄和叠氮化钠在乙醇中反应制备了苄叠氮,进而与对甲氧基苯乙炔进行1,3-偶极环加成反应合成了未见报道的1-苄基-4-(4-甲氧基)-苯基-1,2,3-三唑,产率达到了48%,产物结构经NMR和MS确认。 Benzyl azide was synthesized in ethyl alcohol by substitution reaction with benzyl chloride and sodium azide, and then 1-benzyl-4-(4-methyloxy)phenyl-1, 2, 3-triazole was prepared by 1,3-dipolar cycloaddition of benzyl azide and 4-methoxyphenylacetylene, with the yield of 48 %. The structures of the products were characterized by NMR and MS.
出处 《广州化工》 CAS 2009年第1期84-84,91,共2页 GuangZhou Chemical Industry
关键词 三唑 环加成反应 合成 triazole 1, 3-dipolar cycloaddition synthesis
  • 相关文献

参考文献4

  • 1Chunyang Jin, Heman A. Navarro, F. Ivy Carroll. Synthesis and receptor binding properties of 2 13 :alkynyl and 213 -(1,2,3-triazol) substituted 313 -(substituted phenyl) tropane derivatives[J]. Bioorg. Med. Chem. 2008, 16(10): 5529-5535.
  • 2Caroline C, Sophie G, Nohad G, et al.Terminal alkyne-funetionalized triazine by Sonogashira coupling:, synthesis of a potential cell signalling inhibitor via click chemistry [J]. Tetra. Lett. 2008, 4999 (29-30): 4542-4545.
  • 3Harda K. A convenient synthesis of 1, 2, 3-triazole with glyoxal [J]. Synlett, 1998, 4: 431-433.
  • 4扈艳红,刘世领,仝钦宇,黄发荣,沈永嘉,齐会民,杜磊.1,3-偶极环加成反应合成1-(取代苄基)-1,2,3-三唑类化合物[J].有机化学,2004,24(10):1228-1232. 被引量:19

二级参考文献5

共引文献18

同被引文献14

  • 1Seo T S,Li Z M,Ruparel H,et al. Click Chemistry to Construct Fluorescent Oligonucleotides for DNA Sequencing[J]. J Org Chem, 2003-68(2): 609-612.
  • 2Shen J,Woodward R,Kedenburg J P, et al. Histone deacetylase inhibitors through click chemistry[J].J Med Chem, 2008-51(23) : 7417 - 7427.
  • 3AlvarezR, VelazquezS, San-FelixA, etal. 1,2-3-Triazole-[2' -5' -bis-O-(tert- Butyldimethylsilyl) β -D-Ribofuranosyl- 3' -spiro-5" -(4' -Amino-1' ,2' - Oxathiole 2" ,2" -Dioxide)](TSAO) Analogues:Synthesis and anti-HIV-1 Activity [J].J Med Chem,1994-37: 4185 -4194.
  • 4Zhang J,Wang X J,Wu D X,et al.Bioconjugated Janus Particles Prepared by in situ Click Chemistry[J].Chem Mater, 2009,21(17)..4012- 4018.
  • 5Ciampi S,Bocking T, Kilian A K,et al. Click Chemistry in Mesoporous Materials: Functionalization of Porous Silicon Rugate Filters[J].Langmuir, 2008,24(11):5888-5892.
  • 6Chelmowski R,Kaer D,Koter S D, et al.Postformation Modification of SAMs:Using Click Chemistry to Functionalize Organic Surfaces[J]. Langmuir, 25(19): 11480 - 11485.
  • 7Pourceau G,Meyer A,Vasseur J J,et al.Synthesis of Mannose and Galactose Oligonucleotide Conjugates by bi-elick Chemistry[J]. J Org Chem.,2009,74(3): 1218- 1222.
  • 8Quader S,Boyd E S,Jenkins D I,et al Multisite Modification of Neomycin B Combined Mitsunobu and Click Chemistry Approach[J].J Org Chem.,2007 72(6): 1962- 1979.
  • 9Breed D R,Thibault R,Xie F,et al. Functionalization of Polymer Microspheres using Click Chemistry [J]. Langmuir, 2009,25(8).. 4370- 4376.
  • 10Tomoe C W, Christensen C, Meldal M. Peptidotriazoles on solid phase:[1,2, 3]-triazoles by regiospecific copper(I)- catalyzed 1-3-dipolar cycloadditions of terminal alkynes to azides[J].J Org Chem, 2002-67(9) : 3057 - 3064.

引证文献1

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