1,1-二(2-氨基甲酰胍)呋喃-2-基甲烷的合成、表征及生物活性

Chioma Don-lawson, Daniel Okechukwu Nwenka, Reminus Okah, kingsley John Orie
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引用次数: 4

摘要

本文报道了1,1-双(2-氨基甲酰胍)呋喃-2-基甲烷的合成、表征及其在特定微生物上的生物活性。第一步是将糠醛与尿素偶联得到1-(2-氨基甲基胍)(呋喃-2-甲基)尿素,随后与更多的尿素在乙醇中回流1小时以获得该产品。中间体和产物经GC-MS、IR、1H-NMR、13C-NMR表征。合成的化合物1,1-二(2-氨基甲酰胍)呋喃-2-基甲烷对大肠杆菌、沙门氏菌和枯草芽孢杆菌有不同程度的生物活性,对金黄色葡萄球菌无活性。糠醛衍生物所具有的生物活性和药理活性证明了其在未来新药开发中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, Characterization and Bioactivity of 1,1-bis(2-Carbamoylguanidino)furan-2-ylmethane
This study reports the synthesis of 1,1-bis(2-Carbamoylguanidino)furan-2-ylmethane, characterisation and bioactivities on selected microorganism. The first step involves the coupling of furfural with urea to obtain 1-((2-carbamoylguanidino)(furan-2-ylmethyl)urea, which was subsequently refluxed with more urea in ethanol for 1 hour to afford the product. Both intermediate and product were characterized by GC-MS, IR, 1H-NMR, 13C-NMR. The synthesized compound1,1-bis(2-carbamoylguanidino)furan-2-ylmethane was bioactive on Escherichia coli, Salmomellatyphi and Bacillus subtilis to different extent and is inactive on Staphylococcus aureus. The presences of bioactive moieties and pharmacological activities have proved the potency of furfural derivatives in the development of novel drug in future.
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