期刊文献+

含氟磺酰胺衍生物的合成与表征 被引量:1

Synthesis of Fluorine-containing Sulfonamide Derivatives
下载PDF
导出
摘要 文章通过三步反应合成了一个含氟磺酰胺衍生物。由2-氟苯胺与2-硝基-3-氟苯磺酰氯生成磺酰胺,然后再分别进行取代和还原反应得到N-(2-氟苯基)-2,2-二甲基-4-氧-2,3,4,9-四氢-1H-咔唑-8-磺酰胺。所合成的化合物通过了1H NMR、MS等光谱方法进行表征。 In this thesis, a sulfonamide derivative was synthesized by a three-step reaction. 2-fluoroaniline was turned into Sulfonamide by sulfonylation with 3-fluro-2-nitrobenzenesulfonyl chloride, and then through substitution and reduction reaction to give N-(2-fluorophenyl)-2,2-dimethyl-4-oxo-2,3,4,9-tetrahydro-lH- carbazole-8-sulfonamide, which was characterized by 1 HNMR and MS spectroscopy.
出处 《广东化工》 CAS 2014年第20期13-14,25,共3页 Guangdong Chemical Industry
基金 2013年国家大学生创新训练计划项目
关键词 磺酰胺 还原 合成 表征 sulfbnamide reduction synthesis characterized
  • 相关文献

参考文献9

  • 1王小玲,王宪龙,耿蓉霞,周成合.含磺酰胺结构的抗微生物药物研究进展[J].中国新药杂志,2010,19(22):2050-2059. 被引量:11
  • 2Zani F,Incerti M,Ferretti R,et al.Hybrid molecules between benzensulfonamides and active antimicrobial benzoisothiazol-3-ones[J].Eur.J.Med.Chem.,2009,44(6):2741-2747.
  • 3Talath S,Gadad A K.Synthesis,antibacterical and antitubercular activities of some 7-[4-(5-amino-[1,3,4]thiadiazole-2-sulfonyl)-piperazin-yl]fluoroquinolonic derivatives[J].Eur.J.Med.Chem.,2006,41(8):918-924.
  • 4Kim S J,Jung M H,Yoo K H,et al.Synthesis and antibacterial activities of novel oxazolidinones having cyclic sulfonamide moieties[J].Bioorg Med ChemLett,2008,18(21):5815-5818.
  • 5Rostom SAF.Synthesis and in vitro antitumor evaluation of some indeno[1,2-c]-pyrazol(in)es substituted with sulfonamide,sulfonylurea(-thiourea) p harmacophores,and some derived thazole ring systems[J].Bioorg Med Chem,2006,14(19):6475-6485.
  • 6Kamel M M,Ali H I,Anwar M M,et al.Synthesis,antitumor activity and molecular docking study of novel sulfonamide-schiffs bases,thiazolidinones,benzothiazinones and their C-nucleoside derivatives[J].Eur.J.Med.Chem.,2010,45(2):572-580.
  • 7宋浩斌,曹胜利,郑晓霖.磺酰胺类抗肿瘤药物研究进展[J].中国新药杂志,2009,18(2):108-115. 被引量:13
  • 8Alqasoumi S I,AI-Taweel A M,Alafeefy A M,et al.Novel quinolines and pyrimido[4,5-b]quinolines bearing biologically active sulfonamide moiety as a new class ofantitumor agents[J].Eur J Med Chem,2010,45(2):738-744.
  • 9Carta F,Maresca A,Covarrubias A S,et al.Carbonic anhydrase inhibitors.Characterization and inhibition studies of the most active β-carbonic anhydrase from mycobacterium tuberculosis,Rv3588c[J].Bioorg Med Chem Lett,2009,19(23):6649-6654.

二级参考文献35

  • 1曹胜利,郭燕文,王先波.抗叶酸剂类抗肿瘤药物的研究进展[J].中国新药杂志,2007,16(10):747-753. 被引量:9
  • 2CHO SY, FOX E, MCCULLY C, et al. Plasma and cerebrospi- nal fluid pharmacokinetics of intravenously administered ABT-751 in non-human primates [ J ]. Cancer Chemother Pharmacol, 2007, 60(4) : 563 -567.
  • 3CHANG JY, HSIEH HP, CHANG CY, et al. 7-Aroyl-aminoindoline-1-sulfonamides as a novel class of potent antitubulin agents [J]. J Med Chem, 2006, 49(23): 6656-6659.
  • 4HU LX, LI ZR, LI Y, et al. Synthesis and structure-activity relationships of carbazole sulfonamides as a novel class of antimitotic agents against solid tumors[ J]. J Med Chem, 2006, 49(21 ) : 6273 - 6282.
  • 5HU LX, LI ZR, WANG YM, et al. Novel pyridinyl and pyrimidinylcarbazole sulfonamides as antiproliferative agents [ J ]. Bioorg Med Chem Lett, 2007, 17(5) : 1193 -1196.
  • 6KAMAL A, KHAN MNA, REDDY KS, et al. Synthesis of a new class of 2-anilino substituted nicotinyl arylsulfonylhydrazides as potential anticancer and antibacterial agents [ J ]. Bioorg Med Chem, 2007, 15(2): 1004-1013.
  • 7TALBOT DC, VON PAWEL J, CATTELL E,et al. A randomized phase Ⅱ pharmacokinetic and pharmacodynamic study of indisulamas second-line therapy in patients with advanced nonsmall cell lung cancer[ J]. Clin Cancer Res, 2007, 13 (6) : 1816 - 1822.
  • 8OWA T, YOSHINO H, OKAUCHI T, et al. Synthesis and biological evaluation of N-(7-indolyl) -3-pyridinesulfonamide derivatives as potent antitumor agents [ J ]. Bioorg Med Chem Lett, 2002, 12(16) : 2097 -2100.
  • 9BOUISSANE L, EL KAZZOULI S, LIEONCE S, et al. Synthesis and biological evaluation of N-(7-indazolyl) benzenesulfonamidc derivatives as potent cell cycle inhibitors[ J]. Bioorg Med Chem, 2006, 14(4) : 1078 - 1088.
  • 10LIN RH, CONNOLLY PJ, WETTER SK, et al. Substituted triazole diamine derivatives as kinase inhibitors: US, 6924302B2 [P]. 2005-08-02.

共引文献20

同被引文献3

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