纤维素负载的丙基胺/钼酸盐复合物:合成吡嘧啶衍生物的新型可回收纳米催化剂

IF 0.9 Q4 CHEMISTRY, PHYSICAL Current Organocatalysis Pub Date : 2022-05-25 DOI:10.2174/2213337209666220525161703
Raziyeh Keshavarz, Mahnaz Farahi
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引用次数: 0

摘要

碳基材料由于其独特的性质,如重量轻、形式多样、掺杂杂原子的能力、低成本和易于加工,是适用于多相催化剂的载体。其中,纤维素作为最丰富、最可再生的有机聚合物之一,在许多有机原料中占有重要地位。吡嘧啶衍生物由于其高生物活性而引起了药物化学家和生物化学家的兴趣。此外,它们在许多天然化合物和药用分子中发挥着最基本的结构作用。由于具有多种生物活性的吡啶,吡啶环系统已成为许多药物中重要的基本成分也就不足为奇了。本研究以纤维素为非均相载体,制备了一种高效的固体催化剂。纤维素作为最丰富的有机聚合物,是实现这一目的的合适材料。然后,通过在这种碳基材料的表面上用连接体固定聚氧化钼,我们成功地制备了Cell@(CH2)3N=Mo[Mo5O18]纳米催化剂。该催化剂的结构和性能通过包括FT-IR、XRD、EDS图谱、FE-SEM和TGA在内的各种分析得到了证实,并通过芳醛、丙二腈和巴比妥酸之间的多组分反应在制备Pyrano[2,3-d]嘧啶衍生物中的应用来评估其功效。这项研究的结果表明,这种新型无毒的有机-无机杂化纳米催化剂在短时间内以适当的效率提供了所需的产物。本方案的关键特征包括催化剂的可重复使用性、易于回收、环境反应条件以及使其经济和可持续的简单后处理程序。
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Cellulose Supported Propylamine/Molybdate Complex: A Novel and Recyclable Nanocatalyst for the Synthesis of Pyranopyrimidine Derivatives
Carbon-based materials, due to their unique properties such as lightweight, many varieties of forms, doping capability with hetero atoms, low cost, and ease of processability, are suitable support, for heterogeneous catalysts. Among them, cellulose, as one of the most abundant and renewable organic polymers, preserves a key position in many organic raw materials. Pyranopyrimidine derivatives, due to their high biological activity are of interest to both medicinal chemists and biochemists. Moreover, they play the most fundamental structural role in many natural compounds and medicinally useful molecules. Owing to the great variety of biologically active pyridines, it is not surprising that the pyridine ring system has become a vital basic component in many pharmaceutical agents. In this study, cellulose as heterogeneous support was used to prepare an efficient solid catalyst. Cellulose, as the most abundant organic polymer, is a suitable material for this purpose. Then, by immobilizing polyoxomolybdate by a linker on the surface of this carbon-based material, we succeeded in producing Cell@(CH2)3N=Mo[Mo5O18] nanocatalyst. The structure and properties of this catalyst were confirmed by various analyzes including FT-IR, XRD, EDS-map, FE-SEM, and TGA, and its efficacy was evaluated by its use in the preparation of Pyrano[2,3-d]pyrimidine derivatives through a multicomponent reaction between aryl aldehydes, malononitrile, and barbituric acid. The results of this study showed that this new and non-toxic organo-inorganic hybrid nanocatalyst provides the desired products in a short time and with appropriate efficiency. The key features of the present protocol include reusability of the catalyst, ease of recovery, ambient reaction conditions, and simple work-up procedure that make it economic and sustainable.
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来源期刊
Current Organocatalysis
Current Organocatalysis CHEMISTRY, PHYSICAL-
CiteScore
2.00
自引率
0.00%
发文量
28
期刊介绍: Current Organocatalysis is an international peer-reviewed journal that publishes significant research in all areas of organocatalysis. The journal covers organo homogeneous/heterogeneous catalysis, innovative mechanistic studies and kinetics of organocatalytic processes focusing on practical, theoretical and computational aspects. It also includes potential applications of organocatalysts in the fields of drug discovery, synthesis of novel molecules, synthetic method development, green chemistry and chemoenzymatic reactions. This journal also accepts papers on methods, reagents, and mechanism of a synthetic process and technology pertaining to chemistry. Moreover, this journal features full-length/mini review articles within organocatalysis and synthetic chemistry. It is the premier source of organocatalysis and synthetic methods related information for chemists, biologists and engineers pursuing research in industry and academia.
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