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首页> 外文期刊>Russian Chemical Bulletin >Synthesis of nitro,nitroso,azo,and azido derivatives of (4-R~1-5-R~2-1,2,3-triazol-1-yl)-1,2,5-oxadiazolesby oxidation and diazotization of the corresponding amines
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Synthesis of nitro,nitroso,azo,and azido derivatives of (4-R~1-5-R~2-1,2,3-triazol-1-yl)-1,2,5-oxadiazolesby oxidation and diazotization of the corresponding amines

机译:硝基苯的氧化和重氮化反应合成(4-R〜1-5-R〜2-1,2,3-三唑-1-基)-1,2,5-恶二唑的硝基,亚硝基,偶氮和叠氮基衍生物相应的胺

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摘要

Nitro-,nitroso-,and azo-1,2,5-oxadiazoles with 4-R~1-5-R~2-1,2,3-triazol-1-yl substituents were synthesized by oxidation of amino-(1,2,3-triazol-1-yl)-1,2,5-oxadiazoles(aminotri-azolylfurazans).Azido-1,2,5-oxadiazole was prepared by diazotization of amino(triazo-lyl)furazan followed by treatment of the diazonium salt with sodium azide.Depending on the nature of the substituents and the reagent,triazolylfurazans can undergo destruction to give amino-R-furazans(R = NO_2,N_3,aminofurazanylazo),the amino group being formed from the triazole ring.
机译:通过氨基-(1的氧化,合成具有4-R〜1-5-R〜2-1,2,3-三唑-1-基取代基的硝基,亚硝基和偶氮1,2,5-恶二唑1,2,3-三唑-1-基)-1,2,5-恶二唑(氨基三唑基呋喃山)通过将氨基(三唑基)呋喃山酰胺重氮化然后处理重氮盐与叠氮化钠。根据取代基和试剂的性质,三唑基呋喃根可以被破坏,生成氨基-R-呋喃唑烷(R = NO_2,N_3,氨基呋喃唑基偶氮),氨基由三唑环形成。

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