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一种用于合成吖啶-1,8-二酮和2-氨基-3-氰基-4-吡喃衍生物的超分子磁性多功能三联吡啶V接枝壳聚糖有机催化剂。

A supramolecular magnetic and multifunctional Titriplex V-grafted chitosan organocatalyst for the synthesis of acridine-1,8-diones and 2-amino-3-cyano-4-pyran derivatives.

作者信息

Hassanzadeh Najmeh, Dekamin Mohammad G, Valiey Ehsan

机构信息

Pharmaceutical and Heterocyclic Compounds Research Laboratory, Department of Chemistry, Iran University of Science and Technology Tehran 1684613314 Iran

出版信息

Nanoscale Adv. 2024 Oct 2;7(1):99-123. doi: 10.1039/d4na00264d.

DOI:10.1039/d4na00264d
PMID:39502107
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11533062/
Abstract

In this research, a new supramolecular magnetic modified chitosan, namely, FeO@CS-TDI-Titriplex V, was designed and prepared conveniently by grafting diethylenetriaminepentaacetic acid (Titriplex V) onto a biopolymeric chitosan backbone having urethane, urea, ester and amide functional groups. The obtained magnetic biopolymeric nanomaterial was properly characterized by different spectroscopic, microscopic or analytical methods including FTIR spectroscopy, EDX spectroscopy, XRD, FESEM, TG-DTA and VSM. The application of the supramolecular FeO@CS-TDI-Titriplex V nanocomposite as a heterogeneous solid acidic organocatalyst was investigated to promote the three-component synthesis of both acridinediones and 2-amino-3-cyano-4-pyran derivatives as important pharmaceutical scaffolds under green conditions. The obtained nanomaterial exhibited proper catalytic activity in the above mentioned transformations through multicomponent reaction (MCR) strategies. The reactions proceeded very well in the presence of the FeO@CS-TDI-Titriplex V solid acid nanomaterial in EtOH to afford the corresponding acridinediones and 2-amino-3-cyano-4-pyran derivatives in high to excellent yields. The key advantages of the present protocol include the use of a renewable, biopolymeric and biodegradable solid acid as well as a simple procedure for the preparation of the hybrid material. Furthermore, the FeO@CS-TDI-Titriplex V nanomaterial was used four times with a slight decrease in its catalytic activity.

摘要

在本研究中,通过将二乙烯三胺五乙酸(滴定三乙铵五醋酸)接枝到具有氨基甲酸酯、尿素、酯和酰胺官能团的生物聚合物壳聚糖主链上,方便地设计并制备了一种新型超分子磁性改性壳聚糖,即FeO@CS-TDI-滴定三乙铵五醋酸。通过傅里叶变换红外光谱(FTIR)、能谱分析(EDX)、X射线衍射(XRD)、场发射扫描电子显微镜(FESEM)、热重-差示热分析(TG-DTA)和振动样品磁强计(VSM)等不同的光谱、显微镜或分析方法对所得磁性生物聚合物纳米材料进行了恰当表征。研究了超分子FeO@CS-TDI-滴定三乙铵五醋酸纳米复合材料作为多相固体酸性有机催化剂在绿色条件下促进吖啶二酮和2-氨基-3-氰基-4-吡喃衍生物这两种重要药物支架的三组分合成的应用。所得纳米材料通过多组分反应(MCR)策略在上述转化中表现出适当的催化活性。在乙醇中,FeO@CS-TDI-滴定三乙铵五醋酸固体酸纳米材料存在下,反应进行得非常顺利,以高至优异的产率得到相应的吖啶二酮和2-氨基-3-氰基-4-吡喃衍生物。本方法的关键优势包括使用可再生、生物聚合物且可生物降解的固体酸以及制备杂化材料的简单程序。此外,FeO@CS-TDI-滴定三乙铵五醋酸纳米材料使用了四次,其催化活性略有下降。

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