首页> 外文期刊>Journal of the Brazilian Chemical Society >Cascade Synthesis of Thieno[2,3-b]pyridines by Using Intramolecular Cyclization Reactions of 3-Cyano-2-(organylmethylthio)pyridines
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Cascade Synthesis of Thieno[2,3-b]pyridines by Using Intramolecular Cyclization Reactions of 3-Cyano-2-(organylmethylthio)pyridines

机译:通过3-氰基-2-(有机基甲硫基)吡啶的分子内环化反应级联合成噻吩并[2,3-b]吡啶

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>2-Amino-4-aryl-6-mercaptopyridine-3,5-dicarbonitriles as starting materials have been prepared by reducing of 2-amino-4-aryl-6-(phenylthio)pyridine-3,5-dicarbonitrile derivatives which were synthesized on stepwise one-pot three component reaction of malononitrile, aldehydes and thiophenol in the presence of base catalysts such as triethylamine, high surface area (HSA) MgO or nanocrystalline magnesium oxide. Alkylation of 2-amino-4-aryl-6-mercaptopyridine-3,5-dicarbonitriles with α-halogen compounds in presence of sodium alkoxide as base catalyst followed with cyclization afforded the thieno[2,3-b]pyridine derivatives in excellent yields and in a short reaction time.
机译:通过还原2-氨基-4-芳基-6-(苯硫基)吡啶-3,5-二碳腈衍生物,制备了作为原料的2-氨基-4-芳基-6-巯基吡啶-3,5-二碳腈。它们是在碱催化剂(例如三乙胺,高表面积(MgO)或纳米晶状氧化镁)的存在下,通过丙二醛,醛和硫酚的逐步一锅三组分反应合成的。在碱金属钠作为碱催化剂存在下,将2-氨基-4-芳基-6-巯基吡啶-3,5-二腈与α-卤素化合物烷基化,然后环化,得到噻吩[2,3-b]吡啶衍生物,收率高而且反应时间短。

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