以水为溶剂微波辅助合成一种新型嘧啶核希夫碱同系物的方案:绿色合成方法

IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY
D. Karati, K. Mahadik, Dileep Kumar
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引用次数: 1

摘要

研究工作旨在开发可持续的微波辅助合成4-(亚苄基氨基)-6-苯基嘧啶-5-腈同源物的方案。4-(亚苯基氨基)-6-苯嘧啶-5-腈支架是一种新型分子,具有神经退行性、抗微生物、抗癌等多种药理活性。席夫碱同系物被认为是研究的有效药效团。这些活性是由于席夫碱化合物中存在甲亚胺(CH=N)基团。用绿色化学方法合成了不同的嘧啶核席夫碱支架,产率高。通过两步反应制备了4-(亚苄基氨基)-6-苯基嘧啶-5-腈支架。这两个步骤都是微波辅助的。第一步合成中间体4-氨基-6-苯基嘧啶-5-腈。以苯甲醛、丙二腈和甲脒盐酸盐为原料合成了该化合物。反应条件为:温度-1010℃,压力-300W,时间50min。通过在第二步中使希夫碱与各种芳香醛反应得到最终的希夫碱同系物。产率、反应条件和时间消耗对于绿色合成方法来说都是非常可接受的,而不是传统的方案。微波辅助法更有效。反应耗时较少,所有合成化合物的总产率在72-81%的范围内。用不同的光谱方法对合成的同系物进行了表征。主要官能团[甲亚胺]由1611cm-1波长处的IR峰考虑。因此,由于有机溶剂的使用大大减少,这种微波辅助合成方法变得更加环保,从而减少了有害残留物。利用该方案,我们合成了不同的希夫碱同系物,化学产率令人满意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microwave assisted synthetic scheme of a novel Schiff base congeners of pyrimidine nuclei by using water as solvent: green approach of synthesis
The research work aims to develop sustainable microwave-assisted scheme for the synthesis of 4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile congeners. 4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile scaffolds are novel molecules having various pharmacological activities such as neurodegenerative, anti-microbial, anti-cancer. Schiff base congeners are considered as efficient pharmacophores for research. These activities are due to the presence of azomethine (CH=N) group in the Schiff base compounds. To synthesise different novel Schiff base scaffolds of pyrimidine nuclei by green chemistry with good yield. The 4-(benzylidene amino)-6-phenylpyrimidine-5-carbonitrile scaffolds were prepared by two step reactions. Both steps were microwave assisted. The first step was to synthesize 4-amino-6-phenylpyrimidine-5-carbonitrile as intermediate compound. This compound was synthesized by using benzaldehyde, malononitrile and formamidine hydrochloride. The reaction conditions are as following: temperature- 1010C, pressure- 300W, time- 50min. The final Schiff base congeners were obtained by reacting it with various aromatic aldehydes in the second step. The yield, reaction condition, and time consumption all were very acceptable for the green synthetic methods rather than the conventional schemes. Microwave assisted method was more efficient. The reactions were less time consuming and the overall yield of the all-synthesized compounds was in the range of 72-81%. The synthesized congeners were characterized by different spectroscopic methods. The main functional group [azomethine] was considered by the IR peak at 1611 cm-1 wavelength. This microwave assisted synthetic method thus emerges as more eco-friendly due to a much-reduced usage of organic solvents, leading to less harmful residues. Using this scheme, we synthesized different Schiff base congeners with satisfactory chemical yields.
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来源期刊
Current Microwave Chemistry
Current Microwave Chemistry CHEMISTRY, MULTIDISCIPLINARY-
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