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核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

以单(6-氨基-6-脱氧)-β-环糊精修饰的磁性壳聚糖作为一种新型催化剂用于合成吡唑并吡喃嘧啶和吡喃并[2,3-c]吡唑-3-羧酸酯。

Modified magnetic chitosan with mono(6-amino-6-deoxy)-β-cyclodextrin as a novel catalyst toward the synthesis of pyrazolopyranopyrimidines and pyrano[2,3-c]pyrazole-3-carboxylates.

作者信息

Mousavi-Ebadi Maryam, Safaei-Ghomi Javad

机构信息

Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, P.O. Box 87317-51167, Kashan, Islamic Republic of Iran.

出版信息

Sci Rep. 2025 Mar 6;15(1):7863. doi: 10.1038/s41598-025-92249-5.


DOI:10.1038/s41598-025-92249-5
PMID:40050394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11885426/
Abstract

In this study, we successfully fabricated a novel biocomposite composed of 6-amino β-cyclodextrin (CDNH) grafted onto magnetic chitosan (FeO@Cs). This biocomposite was thoroughly characterized using FT-IR, NMR, PXRD, EDX mapping, SEM, TEM, TGA, and VSM techniques. Subsequently, the innovative biocomposite was harnessed to serve as a heterogeneous catalyst to facilitate two series of multicomponent reactions (MCRs) aimed at synthesizing pyrazole-fused heterocycle derivatives. The first reaction involved the combination of hydrazine hydrate, ethyl 3-oxobutanoate, barbituric acid, and various benzaldehyde derivatives. In a separate reaction, dimethyl acetylenedicarboxylate (DMAD), hydrazine hydrate, benzaldehyde derivatives, and malonitrile were used as starting materials. By optimizing the reaction conditions and employing the FeO@Cs@CDNH catalyst, we successfully synthesized valuable pyrazole structures with high yields in both reactions. The ability to optimize conditions and produce new pyrazole structures with impressive yields highlights the effectiveness of using FeO@Cs@CDNH to direct these reactions.

摘要

在本研究中,我们成功制备了一种新型生物复合材料,其由接枝到磁性壳聚糖(FeO@Cs)上的6-氨基β-环糊精(CDNH)组成。使用傅里叶变换红外光谱(FT-IR)、核磁共振(NMR)、粉末X射线衍射(PXRD)、能量散射X射线能谱映射(EDX mapping)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、热重分析(TGA)和振动样品磁强计(VSM)技术对该生物复合材料进行了全面表征。随后,利用这种创新的生物复合材料作为多相催化剂,以促进旨在合成吡唑稠合杂环衍生物的两个系列的多组分反应(MCRs)。第一个反应涉及水合肼、3-氧代丁酸乙酯、巴比妥酸和各种苯甲醛衍生物的组合。在另一个反应中,使用乙炔二羧酸二甲酯(DMAD)、水合肼、苯甲醛衍生物和丙二腈作为起始原料。通过优化反应条件并使用FeO@Cs@CDNH催化剂,我们在两个反应中均成功以高产率合成了有价值的吡唑结构。优化条件并以令人印象深刻的产率生产新的吡唑结构的能力突出了使用FeO@Cs@CDNH指导这些反应的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/65524dc0c738/41598_2025_92249_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/d83994824054/41598_2025_92249_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/205182241ea8/41598_2025_92249_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/5180fa82d5c4/41598_2025_92249_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/e365f74f1214/41598_2025_92249_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/89738c316943/41598_2025_92249_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/7fe304e837d2/41598_2025_92249_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/d05f101fd018/41598_2025_92249_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/3e0f66a547bf/41598_2025_92249_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/03e8c78f37ae/41598_2025_92249_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/7f9a48e06f3c/41598_2025_92249_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/ccd7360b76d2/41598_2025_92249_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/071564815c06/41598_2025_92249_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/65524dc0c738/41598_2025_92249_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/d83994824054/41598_2025_92249_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/205182241ea8/41598_2025_92249_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/5180fa82d5c4/41598_2025_92249_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/e365f74f1214/41598_2025_92249_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/89738c316943/41598_2025_92249_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/7fe304e837d2/41598_2025_92249_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/d05f101fd018/41598_2025_92249_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/3e0f66a547bf/41598_2025_92249_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/03e8c78f37ae/41598_2025_92249_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/7f9a48e06f3c/41598_2025_92249_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/ccd7360b76d2/41598_2025_92249_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/071564815c06/41598_2025_92249_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ed/11885426/65524dc0c738/41598_2025_92249_Fig11_HTML.jpg

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本文引用的文献

[1]
Melamine phosphate-modified magnetic chitosan: a novel biocompatible catalyst for the synthesis of biological tetrahydrodipyrazolopyridine and pyrazolopyranopyrimidine derivatives.

Front Chem. 2024-5-15

[2]
Effect of apricot kernel seed extract on biophysical properties of chitosan film for packaging applications.

Sci Rep. 2024-2-10

[3]
Recent progress in metal assisted multicomponent reactions in organic synthesis.

Front Chem. 2023-9-8

[4]
Fabrication of uniform Pd nanoparticles immobilized on crosslinked ionic chitosan support as a super-active catalyst toward regioselective synthesis of pyrazole-fused heterocycles.

Int J Biol Macromol. 2023-12-31

[5]
Magnetic cobalt oxide supported organosilica-sulfonic acid as a powerful nanocatalyst for the synthesis of tetrahydrobenzo[a]xanthen-11-ones.

Sci Rep. 2023-8-29

[6]
A new role for concentrated solar radiation (CSR) as a renewable heat source for the catalyst-solvent free synthesis of tetrahydrobenzo[b]pyran scaffolds.

Sci Rep. 2023-7-17

[7]
Chitosan bead containing metal-organic framework encapsulated heteropolyacid as an efficient catalyst for cascade condensation reaction.

Sci Rep. 2023-2-16

[8]
Cyclodextrin-metal-organic frameworks in molecular delivery, detection, separation, and capture: An updated critical review.

Carbohydr Polym. 2023-4-15

[9]
Magnetic-propelled FeO-chitosan carriers enhance l-asparaginase catalytic activity: a promising strategy for enzyme immobilization.

RSC Adv. 2018-10-23

[10]
An efficient and green approach for the synthesis of 2,4-dihydropyrano[2,3-]pyrazole-3-carboxylates using BiO/ZrO as a reusable catalyst.

RSC Adv. 2018-5-3

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