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首页> 外文期刊>Catalysis for Sustainable Energy >One-pot synthesis of new Pyrido [2,3-d] Pyrimidine derivatives under ultrasonic irradiation using organo catalyst 4-Dimethylaminopyridine (DMAP)
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One-pot synthesis of new Pyrido [2,3-d] Pyrimidine derivatives under ultrasonic irradiation using organo catalyst 4-Dimethylaminopyridine (DMAP)

机译:使用有机催化剂4-二甲基氨基吡啶(DMAP)在超声辐射下一锅合成新的吡啶并[2,3-d]嘧啶衍生物

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The one-pot synthesis of pyrido[2,3-d]pyrimidine derivatives has been reported viaKnoevenagel-Michal addition pathways using substitutedaromatic aldehydes, Cyanoacetamide and 6-aminouracilin N,N-dimethylformamide (DMF) solvent, with4-dimethylaminopyridine (DMAP) as new organo catalystcatalyst under ultrasonic irradiation. The results showedthat a series of aromatic aldehydes were effectively used toprepare the targeted pyrido [2, 3-d] pyrimidine derivativeswith good to excellent yields (81-93 %) with no major effecton the yield of product by electron donating/withdrawingsubstituents. Short reaction time, environment friendlyprocedure, excellent yields, inexpensive and readilyavailable catalyst are the advantages of this procedure.All synthesized compounds were characterized by IR,1HNMR, 13CNMR and mass spectral data.
机译:据报道,使用取代的芳族醛,氰乙酰胺和6-氨基尿嘧啶N,N-二甲基甲酰胺(DMF)溶剂,以4-二甲基氨基吡啶(DMAP)为原料,通过Knoevenagel-Michal加成途径一锅合成吡啶并[2,3-d]嘧啶衍生物。超声辐射下的新型有机催化剂结果表明,一系列芳香醛可以有效地用于目标吡啶基[2,3-d]嘧啶衍生物的再生,其收率良好至优异(81-93%),而对给电子/撤出取代基的产物收率没有重大影响。该方法的优点是反应时间短,环境友好,产率高,价格便宜且易于获得。这是所有合成化合物的特征。通过IR,1 HNMR,13 CNMR和质谱数据对化合物进行了表征。

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