Fahmy Amin F M, El-Sayed Amira A, Hemdan Magdy M
Department of Chemistry, Faculty of Science, Ain Shams University, 11566 Abbasia, Cairo, Egypt.
Chem Cent J. 2016 Oct 6;10:59. doi: 10.1186/s13065-016-0205-9. eCollection 2016.
Mechano heterocyclic chemistry (MCH) is a recent quickly growing technique in the synthesis of heterocycles and draws the attention of heterocyclic chemists towards the uses of grindstone technique in a solvent free green efficient synthesis of many heterocyclic systems. On the other hand, multicomponent approach has opened the door for the rapid and efficient one-step procedures to synthesize a wide range of complex targets. Azlactones have been reported to exhibit a wide range of pharmaceutical properties including immune suppressive, anticancer. Antimicrobial, antitumor, anti-inflammatory and antiviral. It also used as useful synthons in the synthesis of several small molecules, including amino acids and peptides.
The present work describes an efficient one step green synthesis of 4-arylidene-2-phenyl-5(4H)-oxazolones (azlactones) via the multi-component synthesis by the mechanochemical grinding of glycine, benzoyl chloride, an aromatic aldehyde and fused sodium acetate in the presence of drops of acetic anhydride. This process is green, simple to handle, step and atom efficient, economical and environmentally friendly, because it does not require a reaction solvent or heating, we introduced the yield economy [YE] as a metric to assess the conversion efficiency of grinding and conventional synthetic reactions of azlactones. The structures of the newly synthesized compounds were elucidated by elemental and spectral analyses.
In conclusion, we have developed a simple, efficient and eco-friendly strategy for facile synthesis of azlactones. The key advantages of this strategy, over conventional approach, include its simple, solvent free conditions, as well as its facile work-up, high yield economy and environmental friendliness. It is also successful in achieving three of the green chemistry objectives of a solvent free operation, high atom economy and step efficient. Thus, combining the features of both economic and environmental advantages.Graphical abstractAn efficient one step green synthesis of azlactones via multicomponent synthesis by a mechanochemical grinding.
机械杂环化学(MCH)是近年来在杂环合成中迅速发展的一项技术,它吸引了杂环化学家关注磨盘技术在许多杂环体系的无溶剂绿色高效合成中的应用。另一方面,多组分方法为快速高效地一步合成多种复杂目标化合物打开了大门。据报道,乙内酰脲具有广泛的药理特性,包括免疫抑制、抗癌、抗菌、抗肿瘤、抗炎和抗病毒。它还用作合成几种小分子(包括氨基酸和肽)的有用合成子。
本工作描述了通过在几滴乙酸酐存在下,将甘氨酸、苯甲酰氯、芳香醛和熔融醋酸钠进行机械化学研磨,通过多组分合成高效一步绿色合成4-亚芳基-2-苯基-5(4H)-恶唑酮(乙内酰脲)。该过程绿色、操作简单、步骤和原子经济性高、经济且环保,因为它不需要反应溶剂或加热,我们引入产率经济性[YE]作为评估乙内酰脲研磨和传统合成反应转化效率的指标。通过元素分析和光谱分析阐明了新合成化合物的结构。
总之,我们开发了一种简单、高效且环保的策略来简便地合成乙内酰脲。与传统方法相比,该策略的关键优势包括其简单的无溶剂条件,以及简便的后处理、高产率经济性和环境友好性。它还成功实现了无溶剂操作、高原子经济性和步骤高效性这三个绿色化学目标。因此,兼具经济和环境优势。图形摘要通过机械化学研磨多组分合成高效一步绿色合成乙内酰脲。