期刊文献+

5-硝基-2,3-吲哚二酮的合成

Synthesis of 5- nitroisatin
下载PDF
导出
摘要 本文研究了5-硝基-2,3-吲哚二酮合成的工艺,以水合三氯乙醛等为原料,经胺的烷基化、环合、硝化反应得到产品,并且进行了初步的优化,总收率达到73.6%。该工艺成本低,条件温和,操作简单,适合工业化生产。 We study the synthesis of 5-nitroisatin. 5-nitroisatin was synthesized from trichloroacetaldehyde etc. ,through the alkylation of amine,Cyclization reaction and nitration,and an overall yield of 73. 6%. The process has low cost and sim-ple,simple operation,and suitable for industrialized production.
出处 《江西化工》 2015年第5期88-90,共3页 Jiangxi Chemical Industry
关键词 三氯乙醛 5-硝基-2 3-吲哚二酮 合成 trichloroacetaldehyde 5-nitroisatin Synthesis
  • 相关文献

参考文献5

  • 1Jiang Y, Hansen TV. Isatin 1,2,3 - triazoles as potent inhibitors against caspase - 3 [ J ]. Bioorganic&Medieinal Chemistry Letters, 2011, 21 : 1626 - 1629.
  • 2刘哲林,江涛,任素梅,孔德信.Caspase-3抑制剂研究进展[J].广东药学院学报,2004,20(6):669-670. 被引量:11
  • 3Calvery H O, Noller C R, Adams R. Arsonophenyl - cinchoninic acid ( arsonoeinehophen ) and derivatives [J]. Journal of the American Chemical Society, 1925, 47:3058 - 3060.
  • 4Magiatis P, Polychronopoulos P, Skaltsounis A L, et al. Indirubins deplete striatal monoamines in the Intact and MPTP - treated mouse brain and block kainate -induc - ed kainate - induced striatal astrogliosis [ J ]. Neuro- toxicology and Teratology,2010,32 (2) :212 - 219.
  • 5Vine K L, Locke J IV[, Ranson M, et al. In vitro cytotox- icity evaluation of some substituted isatin derivatives [ J ]. Bioorganie&Medieinal Chemistry, 2007,15 ( 2 ) : 931 - 938.

二级参考文献19

  • 1Han YX, Giroux A, Erich L, et al. Discovery of novel aspartyl ketone dipeptides as potent and selective caspase-3 inhibitors[J]. Bioorg Med Chem Lett,2004,14(3):805.
  • 2Karanewsky DS, Xu B, Linton SD,et al. Conformationally constrained inhibitors of caspase-1 (interleukin-1 beta converting enzyme) and of the human CED-3 homologue caspase-3 (CPP32, apopain) [J]. Bioorg Med Chem Lett,1998,8(19): 2 757.
  • 3Linton SD, Karanewsky DS, Ternansky RJ,et al. Acyl dipeptides as reversible caspase inhibitors. Part 1: initial lead optimization[J]. Bioorg Med Chem Lett,2002,12(20): 2 969.
  • 4Linton SD, Karanewsky DS, Ternansky RJ,et al. Acyl dipeptides as reversible caspase inhibitors. Part 2: further optimization[J]. Bioorg Med Chem Lett ,2002,12(20): 2 973.
  • 5Ullman BR, Aja T, Deckwerth TL, et al. Structure-activity relationships within a series of caspase inhibitors: effect of leaving group modifications[J]. Bioorg Med Chem Lett,2003,13(20): 3 623.
  • 6Guo ZM, Xian M, Zhang W,et al. N-nitrosoanilines: a new class of caspase-3 inhibitors[J]. Bioorg Med Chem,2001,9(1): 99.
  • 7Wang Y, Huang JC, Zhou ZL, et al. Dipeptidyl aspartyl fluoromethyl ketones as potent caspase-3 inhibitors: SAR of the P2 amino acid[J]. Bioorg Med Chem Lett, 2004, 14(5):1 269.
  • 8Lee D, Long SA, Murray JH, et al. Potent and selective nonpeptide inhibitors of caspases 3 and 7[J]. J Med Chem, 2001, 44(12): 2015.
  • 9Lee D, Long SA, Murray JH, et al. Potent and selective nonpeptide inhibitors of caspases 3 and 7 inhibit apoptosis and maintain cell functionality[J]. J Biol Chem, 2000,275(21): 16 007.
  • 10Kim ES, Yoo SE, Yi KY, et al. Design, Syntheses and biological evaluations of nonpeptidic caspase 3 Inhibitors[J]. Bull Korean Chem Soc, 2002, 23(7):1 003.

共引文献10

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