期刊文献+

4-氨基哒嗪的合成

Synthesis of 4-amino pyridazine
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摘要 3,6-二氯哒嗪和氯气反应生成3,4,6-三氯哒嗪,再用甲醇和氨气氨化合成3,6-二氯-4-氨基哒嗪,最后经催化脱氯制得目标化合物4-氨基哒嗪,摩尔总收率达48.2%。通过熔点测定、1H NMR及质谱确认产品。 The starting material 3,6-dichloropyridazine reacts with chlorine to produce 3,4,6-trichloropyridazine.And then followed with methanol and ammonia to synthesize 3,6-dichloro-4-aminopyridazine,which via catalytic dechlorination reaction achieves object compound 4-amino pyridazine and gave a 48.2% overall molar yield.Its structure was analyzed and characterized through melting point testing,1H NMR and mass spectrometry.
出处 《应用化工》 CAS CSCD 2013年第8期1489-1491,共3页 Applied Chemical Industry
基金 西安市科技创新基金(CX08063)
关键词 3 6-二氯-4-氨基哒嗪 4-氨基哒嗪 合成 收率 3 6-dichloro-4-amino pyridazine 4-amino pyridazine synthesis yield
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参考文献10

  • 1辛炳炜.3-溴-6-甲基哒嗪的合成[J].化学试剂,2008,30(2):143-144. 被引量:12
  • 2Worms P,Kan J P,Wermuth C G,et al.Dopamine-like ac-tivities of an aminopyridazine derivative,CM 30366:A be-havioural study[J].Naunyn-Schmiedeberg’s Archives ofPharmacology,1986,334(3):246-252.
  • 3Heinisch G,Kopelent H.4 Pharmacologically active pyr-idazine derivatives.Part 2[J].Progress in MedicinalChemistry Elsevier Amsterdam,1992,29:141-183.
  • 4Wermuth C G.Search for new lead compounds:The exam-ple of the chemical and pharmacological dissection ofaminopyridazines[J].J Heterocycl Chem,1998,35(5):1091-1100.
  • 5Schumacher C,Steinberg R,Kan J P,et al.Pharmacologi-cal characterization of the aminopyridazine SR 95639A,aselective M1 muscarinic agonist[J].European Journal ofPharmacology,1989,166(2):139-147.
  • 6Velentza A V,Wainwright M S,Zasadzki M,et al.Anaminopyridazine-based inhibitor of a pro-apoptotic proteinkinase attenuates hypoxia-ischemia induced acute braininjury[J].Bioorganic&Medicinal Chemistry Letters,2003,13:3465-3470.
  • 7Chanh P H,Lasserre B,Kaiser R,et al.Aminopyridazinederivatives and TXA2-PGI2 balance[J].Prostaglandins,Leukotrienes and Essential Fatty Acids,1990,40(2):143-148.
  • 8Rival Y,Hoffmann R,Didier B,et al.5-HT3 Antagonistsderived from aminopyridazine-type muscarinic M1 agonists[J].J Med Chem,1998,41:311-317.
  • 9Craft J M,Van Eldik L J,Zasadzki M,et al.Aminopyr-idazines attenuate hippocampus-dependent behavioral def-icits induced by humanβ-amyloid in a murine model ofneuroinflammation[J].Journal of Molecular Neuro-science,2004,24:115-122.
  • 10施祖德,左桂权.一种高纯度3,4,6-三氯哒嗪的制备方法及其产品的应用:CN,1958577[P].2007-05-09.

二级参考文献5

  • 1OVERBERGER C G, BYRD N R, MESROBIAN R B. Azo compounds, investigation of the structure of the products from the reaction of acetonylacetone and hydrazine [ J ]. J. Am. Chem. Soc. ,1956,78(5):1 961-1 965.
  • 2HASSAN J, SEVIGNON M, GOZZI C, et al. Aryl-aryl bond formation one century after the discovery of the Ullmann reaction[J]. Chem. Rev, ,2002,102(5):1 359-1 469.
  • 3MAES B U W,LEMIERE G L F,DOMMISSE R,et al.A new approach towards the synthesis of 3-amino-6-(hetero) arylpyridazines based on palladium catalyzed cross-coupling reactions[J]. Tetrahedron ,2000,56:1 777-1 781.
  • 4OVEREND W G, WIGGINS L F. The conversion of sucrose into pyridazine derivatives, part I. 3-sulphanilamido-6-methylpyridazine[ J]. J. Chem. Soc. , 1947,27:239-243.
  • 5喻爱明,刘天麟,王立坤.哒嗪-3-酮类化合物的合成进展[J].合成化学,1997,5(2):141-146. 被引量:1

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