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6-(N-吡啶)氨基-1-甲基-1H-吲唑类化合物的设计与合成

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摘要 以3-甲基-6-硝基吲唑为起始原料,经N-甲基化、还原、烷基化反应得到三个未见文献报道的6-(N-吡啶)氨基吲唑类化合物。目标化合物及中间体结构经1H-NMR、ESI-MS确证。
作者 刘娥
出处 《荆楚理工学院学报》 2015年第2期29-31,共3页 Journal of Jingchu University of Technology
基金 湖北省教育厅科学技术研究项目(Q20144304) 荆楚理工学院校级科研项目(ZR201411)
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参考文献8

  • 1FOLKMAN J. What is the evidence that tumors are angiogenesis dependent [ J]. J Natl Cancer Inst, 1990,82 (1) :4 -6.
  • 2YOKOYAMA Y, SATO S, FUTAGAMI M, et al. Prognostic significance of vascular endothelial growth factor and its receptors in endometrial carcinoma[ J]. Gynecol Onco1,2007,77 (3) :413 -418.
  • 3FERRARA N. VEGF and the quest for tumour angiogenesis factors [ J ]. Nature Rev Cancer,2002,2 (7) :795 -803.
  • 4FERRARA N. Vascular endothelial growth factor as a target for anticancer therapy[J]. Oncologist,2004 ,9( 1 ) :2 - 10.
  • 5HARRIS P A, BOLOOR A, CHEUNG M ,et al. Discovery of 5 - [ [4 - [ ( 2,3 -dimethyl -2H -indazol -6 -yl ) methyl- amino ] - 2 - pyrimidinyl ] amino ] - 2 - methyl - benzenesulfonamide ( pazopanib ), a novel and potentvascular endothelial growth factor receptor inhibitor[J]. J Med Chem,2008,51 (15) :4 632 -4 640.
  • 6龙丽,刘冰妮,刘默,储德清,祁浩飞,王景阳,刘登科.新型N-(2'-芳胺嘧啶-4'-基)-N,2,3-三甲基-2H-吲唑-6-胺衍生物的合成及其抗肿瘤活性[J].合成化学,2011,19(6):723-726. 被引量:4
  • 7Yuping Jia, Jian Zhang, Jinhong Feng, et al. Design, Synthesis and Biological Evaluation of Pazopanib Derivatives as Antitu- mor Agents[ J]. Chem Biol Drug Des,2014,83:306 - 316.
  • 8张晓凯,刘登科,刘冰妮,刘默,王平保.新型含嘧啶环吲唑衍生物的合成及初步生物活性研究[J].中国药物化学杂志,2013,23(1):15-20. 被引量:2

二级参考文献23

  • 1Balardi P G, Cacciari B, SpaUuto G, et al. A new synthetic approach to indazole synthesis[ J]. Synthesis, 1997 : 1140 - 1142.
  • 2Harris P A, Boloor A, Cheung M, et 02. Discovery of 5- 【 { [ 4- (2,3 -dimethyl-2H-indazol-6-yl ) methylamino ] - 2-pyrimidinyl } amino ] -2-methyl-benzenesulfonamide ( Pazopanib), a nobel and potent vascular endothelial growth factor receptor inhibitor [ J ]. J Med Chem, 2008,51 (7) : 4632 - 4640.
  • 3Sorbera L A, Bol6s J, Serradell N. Pazopanib hydro- chloride [ J ]. Drugs of the Future, 2006,31 (7) : 585 - 589.
  • 4Pandite A N, Whitehead B F, Suttle A B, et al. Cancer treatment method [ P ]. WO, 2007 064 753, 2007.
  • 5Boloor A, Cheung M. Chemieal process[ P]. WO 03 106 416,2003.
  • 6Boloor A, Cheung M, Davis R, et al. Pyrimidineam- ines as angiogenesis modulators [ P ]. WO 02 059 110, 2002.
  • 7Kevin W A, Rachel E T, Takashi I, et al. Monoden- tate phosphines provide highly active catalysts for Pd- catalyzed C - N bond-forming reactions of heteroaro-matic halides/amines and ( H ) N-heteroeycles [ J J. Angew Chem Int Ed,2006,45(39) :6523 -6527.
  • 8Maria J R, Isabel C F, Ricardo C, et al. Synthesis and antioxidant activity evaluation of new 7-aryl or 7- heteroarylamino-2,3-dimethylbenzo[ b] thiophenes ob- tained by Buchwald - Hartwig C - N cross-coupling [ J ]. Bioorh Med Chem ,2007 ,15 :1788 - 1794.
  • 9Krtlger K, TiUaek A, Beller M. Recent innovative strategies for the synthesis of amines: From C - N bond formation to C - N bond activation [ J ]. Chem- suschem,2009,2(8) :715 - 717.
  • 10FOLKMAN J. What is the evidence that tumors are angiogenesis dependent [ J ]. J Natl Cancer Inst, 1990,82( 1 ) :4 -6.

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