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无溶剂条件下 NiFe2O4@SiO2 @氨基葡萄糖磁性纳米粒子:一种新的、温和的、简单有效的合成喹唑啉酮、咪唑并[1,2-a]嘧啶酮和新型酰胺衍生物的方法。

NiFe2O4@SiO2 @amino Glucose Magnetic Nanoparticle under Solvent-free Condition: A New, mild, Simple and Effective Avenue for the Synthesis of Quinazolinone, Imidazo[1,2-a]Pyrimidinone and Novel Derivatives of Amides.

机构信息

Department of Chemistry, Payame Noor University, PO Box 19395-3697 Tehran, Iran.

出版信息

Curr Org Synth. 2020;17(4):304-312. doi: 10.2174/1570179417666200409151330.

Abstract

BACKGROUND

Imidazo[1,2-a]pyrimidinone, quinazolinone and amide derivatives have attracted a lot of interest because of their broad scope of biological and pharmacological activities. There are a lot of methods reported in the literature for their synthesis. Therefore, we became interested in developing a convenient synthetic method for the preparation of imidazoquinazolinone and amide derivatives.

OBJECTIVE

NiFe2O4@SiO2 @glucose amine were synthesized, characterized and have been used for the green, effective and mild multicomponent synthesis of quinazolinones, benzoimidazo[1,2-a]pyrimidinones and amides under solvent-free conditions in short reaction times and excellent yields. To expand of the scope of this avenue, multicomponent synthesis of mono and bis novel amides was tested for the first time. All of the products were characterized by mp, FT-IR, NMR and elemental analysis.

METHODS

Aldehyde (1mmol), 2-amino benzimidazole (1 mmol), dimedone (1mmol) or indane-1,3-dione (1 mmol) for the synthesis of quinazoline or imidazopyrimidinones and arene (1mmol), anhydride (1mmol), 2- aminobenzimidazole (1mmol) for the synthesis of amides in the nanocatalyst NiFe2O4@SiO2@glucose amine (0.15mol%: 0.05g) were stirred by a magnet for the required reaction time. After completion of the reaction, as indicated by TLC, the products were collected and recrystallized from ethanol if necessary.

RESULTS

We present a novel avenue for the synthesis of benzimidazo[1,2-a] pyrimidinones, quinazolinones and amides in the presence of NiFe2O4@SiO2@glucose amine under solvent-free conditions.

CONCLUSION

In conclusion, we developed NiFe2O4@SiO2 @glucose amine-catalysed multicomponent synthesis of quinazolinones and imidazo[1,2-a]pyrimidinones using the reaction of benzaldehyde, dimedone or indane-dione and 2-aminobenzimidazole and multicomponent synthesis of amides using arenes, cyclic anhydrides and 2-aminobenzimidazole by a solvent-free technique. This method proves to be a robust and innovative approach for the synthesis of a biologically important structure. The operational simplicity, the excellent yields of products, ease of separation and recyclability of the magnetic catalyst, waste reduction and high selectivity are the main advantages of this method. Furthermore, this new avenue is cheap and environmentally benign.

摘要

背景

咪唑并[1,2-a]嘧啶酮、喹唑啉酮和酰胺衍生物因其广泛的生物和药理活性而引起了极大的关注。文献中报道了很多合成这些化合物的方法。因此,我们对开发一种方便的合成咪唑并喹唑啉酮和酰胺衍生物的方法很感兴趣。

目的

合成了 NiFe2O4@SiO2@葡萄糖胺,并对其进行了表征,然后在无溶剂条件下,通过该纳米催化剂高效、温和地催化多种组分合成喹唑啉酮、苯并咪唑并[1,2-a]嘧啶酮和酰胺,在短的反应时间内获得了优异的产率。为了拓展该途径的应用范围,我们首次尝试了多种组分合成单酰胺和双酰胺。所有产物均通过熔点(mp)、傅里叶变换红外光谱(FT-IR)、核磁共振(NMR)和元素分析进行了表征。

方法

在纳米催化剂 NiFe2O4@SiO2@葡萄糖胺(0.15mol%:0.05g)存在下,将醛(1mmol)、2-氨基苯并咪唑(1mmol)、二甲基酮(1mmol)或茚满-1,3-二酮(1mmol)用于合成喹唑啉或咪唑并嘧啶酮,以及芳基(1mmol)、酸酐(1mmol)、2-氨基苯并咪唑(1mmol)用于合成酰胺,通过搅拌进行所需的反应时间。反应完成后,根据 TLC 指示,收集产物,如果需要,从乙醇中重结晶。

结果

我们提出了一种在无溶剂条件下,使用 NiFe2O4@SiO2@葡萄糖胺作为催化剂,通过多种组分合成苯并咪唑并[1,2-a]嘧啶酮、喹唑啉酮和酰胺的新方法。

结论

总之,我们开发了一种使用 NiFe2O4@SiO2@葡萄糖胺催化的多种组分合成苯并咪唑并[1,2-a]嘧啶酮、喹唑啉酮和酰胺的方法,该方法通过无溶剂技术使用苯甲醛、二甲基酮或茚满-1,3-二酮与 2-氨基苯并咪唑反应,以及使用芳基、环状酸酐和 2-氨基苯并咪唑进行多种组分合成酰胺。该方法证明是一种合成具有重要生物学结构的稳健且创新的方法。该方法的操作简单、产物产率高、磁性催化剂易于分离和可回收利用、减少废物产生和高选择性是该方法的主要优点。此外,这种新方法成本低廉且环境友好。

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