PEG-400 Catalyzed N-C, O-C & C-S Bond Formations: A Robust Sonication Promoted Synthesis of Benzo[d]oxazole-2 (3H)-thione & Benzo[d]thiazole-2(3H)-thione Hybrids

Aadil Yaseen, M. Waseem, Mahapara Qadir, P. Dar, Shariqah Hijazi, Mir Ashiq Hussain, W. A. Shah
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Abstract

Abstract Herein an efficient and green protocol has been disclosed for the synthesis of biologically competent and structurally simple benzo[d]oxazole-2(3H)-thione/benzo[d]thiazole-2(3H)-thione derivatives. The reaction has been carried out under sonication at 15oC up to 11 hours. Timely progress of the reaction was monitored by using TLC technique. The simple skeletal product with strong biological profile synthesized via simple reaction procedure under complete green conditions is highly useful as per environmental concerns. The unveiled methodology is highly efficient and easy handling as it is devoid of any transition metal catalyst and volatile organic solvent, mostly used for reaction progress. Further, the use of polyethylene glycol, a green catalyst, sonication a selective energy source, better product yield and feasible reaction time are supplementary attributes towards the developed methodology. GRAPHICAL ABSTRACT
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PEG-400催化的N-C, O-C和C-S键形成:一个稳健的超声催化合成苯并[d]恶唑-2(3H)-硫酮和苯并[d]噻唑-2(3H)-硫酮杂化物
本文公开了一种高效、绿色的合成方案,用于合成具有生物活性且结构简单的苯并[d]恶唑-2(3H)-硫酮/苯并[d]噻唑-2(3H)-硫酮衍生物。该反应在15℃的超声波下进行,持续11小时。采用薄层色谱法监测反应的及时进行。在完全绿色的条件下,通过简单的反应程序合成了具有强生物特征的简单骨架产品,对环境问题非常有用。该方法不需要任何过渡金属催化剂和挥发性有机溶剂,主要用于反应过程,因此效率高,易于操作。此外,聚乙二醇(一种绿色催化剂)的使用,超声作为一种选择性能源,更好的产品收率和可行的反应时间是所开发方法的补充属性。图形抽象
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