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4-氨基-7-硝基苯并[1,2,5]噁二唑的合成 被引量:2

Synthesis of 4-Amino-7-nitrobenzo[1,2,5]oxadiazole
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摘要 以 2 ,6-二氯苯胺为原料 ,通过氧化环化、硝化、叠氮化、氨化等 5步反应 ,得到 4-氨基 -7-硝基苯并 [1 ,2 ,5]二唑 ,并对反应条件、精制方法进行了改进。总收率 2 0 .1 %。 Amino 7 nitrobenzo[1,2,5]oxadiazole, an organic fluorescence reagents, was synthesized from 2,6 dichloroaniline by cyclization, nitration, azidation, and then amination with an overall yield of 20.1%.
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2002年第9期425-426,共2页 Chinese Journal of Pharmaceuticals
基金 国家自然科学基金项目 (2 9972 0 0 9)
关键词 4-氨基-7-硝基苯并[1 2 5]恶二唑 合成 2 6-二氯苯胺 氧化环化 硝化 叠氮化 氨化 dichloroaniline 4 amino 7 nitrobenzo[1,2,5]oxadiazole synthesis
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参考文献2

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  • 4Takayama H, Shirakawa S, Kitajima M, et al. Utilization of wieland furoxan synthesis for preparation of 4-aryl-1, 2, 5-oxadiazole-3-ylcarbamate derivatives having potent anti-HIV activity [J]. Bioorg Med Chem Lett, 1996, 6(16): 1 993- 1 996.
  • 5Cereeetto H, Di Maio R, Gonzales M, et al. 1, 2, 5-Oxadiazole N-oxide derivatives and related compounds as potential antitrypanosomal drugs: structure-activity relationships [J]. J Med Chem, 1999, 42(11): 1 941-1 950.
  • 6Genin M J, Allwine D A, Anderson D J, et al. Substituent elects on the antibacterial activity of nitrogen-carbon-linked (azolylphenyl) oxazolidinones with expanded activity against the fastidious gram-negative organisms haemophilus influenzae and moraxella catarrhalis [J]. J Med Chem, 2000, 43(5): 953-970.
  • 7Brockunier L L, Parmee E R, Ok H O, et al. MeO-PEG bounded azide eyeloadditions to alkynyl dipolarophiles [J]. Bioorg Med Chem Lett, 2000, 10(18): 2 111-2 114.
  • 8Parise A, Milelli A, Tumiatti V, eta 1. Preparation, characterization and in vitro evaluation of sterically stabilized liposome containing a naphthalenediimide derivative as anticancer agent [3-]. Drug Delivery, 2013, 9: 1-8.
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