新型2-{4-[2-(n -甲基-2-吡啶氨基)乙氧基]苯基}-5-取代1,3,4-恶二唑文库的微波辅助液相合成

S. Gaonkar, Izuru Nagashima, H. Shimizu
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引用次数: 6

摘要

以氯胺- t为催化剂,以4-[2-(甲基吡啶-2-氨基)乙氧基]苯甲醛和芳基肼为原料,通过氧化环化反应合成了一系列新的2-{4-[2-(n-甲基吡啶-2-氨基)乙氧基]苯基}-5取代的1,3,4-恶二唑。所有步骤均由微波照射辅助。微波使所有这些反应简单、快速、产率高,并且避免了色谱纯化和环境友好的全合成聚焦恶二唑文库。所有合成的化合物都得到了很好的分离,并通过1H NMR、13C NMR和元素分析进行了表征。标题化合物代表了一类新的生物活性杂环化合物。
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Microwave-Assisted Solution Phase Synthesis of Novel 2-{4-[2-(N-Methyl-2-pyridylamino)ethoxy]phenyl}-5-Substituted 1,3,4-Oxadiazole Library
A new series of 2-{4-[2-(N-methyl-2-pyridylamino)ethoxy]phenyl}-5-substituted 1,3,4-oxadiazoles were synthesized by the oxidative cyclization of hydrazones derived from 4-[2-(methylpyridin-2-ylamino)ethoxy]benzaldehyde and aryl hydrazines using chloramine-T as an efficient catalyst. All steps were assisted by microwave irradiation. Microwave enables all these reactions to be simple, rapid, high yielding, and avoid chromatograph purification and led environmentally benign total synthesis of focused oxadiazole library. All the synthesized compounds were isolated in good yield and characterized by 1H NMR, 13C NMR, and elemental analyses. The title compounds represent a novel class of biologically active heterocycles.
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