微波辅助格罗伯克-布莱克本-比奈梅多组分反应合成咪唑并[1,2-a]吡啶-呋喃杂化物,作为白血病、结肠癌和前列腺癌的可能治疗方案

Parth Manvar, Dharmesh Katariya, Amita Vyas, Pooja Bhanderi, R. Khunt
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引用次数: 0

摘要

微波辅助格罗伯克-布莱克本-比奈梅多组分反应的生态友好催化规程,用于合成咪唑并[1,2-a]吡啶-呋喃混合物,作为白血病、结肠癌和前列腺癌的可能治疗方案微波合成已成为一种更经济、更环保地合成有机化合物(如咪唑并[1,2-a]吡啶的衍生物)的有效工具。与传统合成法相比,微波辐射能在更短的时间内激发分子并均匀分配热能。本文研究的主要目的是通过格罗伯克-布莱克本-比奈梅多组分反应制备咪唑并[1,2-a]吡啶-呋喃混合物,采用 PEG 400 在微波辐照下作为绿色方法。在一个密封的微波玻璃瓶中,5-甲基呋喃-2-甲醛 1、2-氨基嗪 2a-g、异氰酸酯 3a-c 在 20 毫摩尔的存在下,我们利用 PEG 400 在微波辐照下进行多组分反应,成功合成了咪唑并[1,2-a]吡啶-呋喃杂化物。通过各种光谱技术确认了这些化合物的结构。与传统的咪唑并[1,2-a]吡啶衍生物制备方法相比,所报告的制备方法更具优势。与传统的回流法相比,所报告的方法更具优势。化合物 4e、4f、4n 和 4o 对白血病、结肠癌和前列腺癌细胞系 RPMI-8226、HCT-116 和 PC-3 的活性分别提高了很多。通过可持续绿色方法利用咪唑并[1,2-a]吡啶-呋喃类化合物的潜力,未来可以设计出更有效、更准确的癌症治疗方法。
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Microwave Assisted Groebke-Blackburn-Bienayme Multicomponent Reaction to Synthesis of Imidazo[1,2-a]pyridine-furan Hybrids as Possible Therapeutic Option for Leukemia, Colon Cancer and Prostate Cancer
Microwave assisted ecofriendly catalytic protocol for the Groebke-Blackburn-Bienayme multicomponent reaction to synthesis imidazo[1,2-a]pyridine-furan hybrids as possible therapeutic option for leukemia, colon cancer and prostate cancer Microwave synthesis has emerged as a potent tool for the more economical and environmentally friendly synthesis of organic compounds, such as derivatives of imidazo[1,2-a]pyridine. Compared to traditional synthesis, microwave radiation causes molecules to be excited and distributes thermal energy evenly in a shorter amount of time. Shorter response times and generally improved efficiency are the benefits of this. The primary objective of the work presented in this article was to prepare imidazo[1,2-a]pyridine-furan hybrids via Groebke-Blackburn-Bienayme multicomponent reaction using PEG 400 in microwave irradiation as green approach. characterized their anticancer activities against leukemia, colon cancer and prostate cancer are evaluated. In a sealed microwave glass vial, 5-methylfuran-2-carbaldehyde 1, 2-aminoazines 2a-g, isocyanides 3a-c in presence of 20mol We have successfully synthesised the imidazo[1,2-a]pyridine-furan hybrids via Groebke-Blackburn-Bienayme multicomponent reaction using PEG 400 in microwave irradiation as green approach. The structures of the compounds were confirmed through various spectroscopic techniques. Characterized their anticancer activities against leukemia, colon cancer and prostate cancer are evaluated. The reported protocol is advantageous over conventional methods of imidazo[1,2-a]pyridine derivatives. The time required for the reaction is much less as compared to the usual requirements of reflux. Compound 4e, 4f, 4n and 4o shows the most increased activity against cell line RPMI-8226, HCT-116 and PC-3 of Leukemia, Colon cancer and Prostate cancer respectively. By using the potential of imidazo[1,2-a]pyridine-furan based compounds via sustainable green approach, more effective and accurate cancer treatments can be designed in future. NA
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