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Scientific Reports volume 13, Article number: 9388 (2023) Cite this article 755 Accesses 1 Citations 2 Altmetric Metrics details In this research article, Zr-MOFs based copper complex as a novel

Scientific Reports volume 13, Article number: 9388 (2023) Cite this article

755 Accesses

1 Citations

2 Altmetric

Metrics details

In this research article, Zr-MOFs based copper complex as a novel heterogeneous and porous catalyst was designed and prepared. The structure of catalyst has verified by various techniques such as FT-IR, XRD, SEM, N2 adsorption–desorption isotherms (BET), EDS, SEM-elemental mapping, TG and DTG analysis. UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 was used as an efficient catalyst in the synthesis of pyrazolo[3,4-b]pyridine-5-carbonitrile derivatives. The aromatization of titled molecules is performed via a cooperative vinylogous anomeric-based oxidation both under air and inert atmospheres. The unique properties of the presented method are short reaction time, high yield, reusability of catalyst, synthesis of desired product under mild and green condition.

Nowadays, metal–organic frameworks as high surface areas materials are a new group of porous materials with potential applications such as gas storage and separation, drug delivery, sensors, batteries, supercapacitors as well as catalytic applications1,2. This framework is a class of organic–inorganic hybrid crystalline materials consisting of metallic nucleus that are linked by strong coordination bonds to organic ligands3,4. The different properties of these porous materials make them a good catalytic candidate for cross coupling, oxidation/reduction, and multicomponent reactions5,6,7,8,9,10. The post-modification method enhances catalytic performance and their variability. According this method, our research team reported a number of catalysts in the synthesis of organic compounds as biological active candidates11,12,13,14,15,16. Copper complex is widely used as catalysts in many organic reactions such as oxidation, cross coupling and catalytic organic reactions17,18,19. Recently, multicomponent reactions have investigated in the presence of palladium, nickel, copper, Fe, and Zr based catalytic systems20,21,22. In this report, a porous and heterogeneous catalyst based on Zr-MOFs with a copper complex is prepared. The simultaneous presence of copper and zirconium will enhance the catalytic application. This new system of porous complexes will lead to a new approach in the design and synthesis of catalysts. Figure 1 shows the final structure of the copper complex based on Zr-MOFs as well as the topology and structure of the UiO-66(Zr) grid.

Structure and morphology of UiO-66(Zr)-NH2 as well as the final structure of a copper complex based on Zr-MOFs.

Diversity of fused N-heterocycles such as pyrazolo[3,4-b]pyridine and 1,2-dihydropyridine-3-carbonitrile containing of indole and pyrazole moieties may be suitable candidates for biological and pharmacological studies23,24,25,26. These materials are suitable candidate for antimicrobial, anticancer, anticonvulsant, antifungal, HIV, anti-tumor, antioxidant, antihypertension and urinary incontinence treatment (Fig. 2a)27,28,29,30,31,32. The target synthesized molecules in this paper may be show biological properties due to the simultaneous presence of indole and pyrazole moieties (Fig. 2b).

(a) The structure of compounds with medicinal and biological properties includes pyrazolo[3,4-b]pyridine, 1,2-dihydropyridine-3-carbonitrile, indole and pyrazole nucleus. (b) Target synthesized molecules with indole and pyrazole moieties.

Anomeric effect (AE) as a fundamental example of stereoelectronic interactions has great educational and research applications33,34,35. It was discovered in 1955 by J. T. Edward in his studies on the carbohydrate chemistry36. The reported theory for the development of anomeric effect (AE) concept had been proposed that sharing the lone pair’s electrons of heteroatoms (X: N, O) to the anti-bonding orbital C–Y (nX → σ*C–Y) weakened it (Fig. 3a). Stereoelectronic effects have also a major role in the oxidation–reduction of susceptible biological compounds such as NADPH/NADP+ (Fig. 3b)37,38,39. Recently, we and our coworkers have reviewed the role of the above-mentioned fundamental concepts comprehensively34,35.

(a) The geminal versus vinylogous anomeric effect in organic synthesis. (b) The structures of NADPH/NADP+.

According to the above-mentioned idea, we have architectonic and synthesis of a copper complex based on Zr-MOFs as a novel heterogeneous and porous catalyst. This porous catalyst was applied for the synthesis of pyrazolo[3,4-b]pyridine-5-carbonitriles by reaction of various aromatic aldehydes (bearing electron-donating and electron-withdrawing groups), ethyl cyanoacetate, 3-(1H-indol-3-yl)-1-phenyl-1H-pyrazol-5-amine or 3-(4-chlorophenyl)-1H-pyrazol-5-amine under solvent-free at 110 °C via a cooperative vinylogous anomeric-based oxidation (Fig. 4).

Preparation of pyrazolo[3,4-b]pyridine-5-carbonitriles using UiO-66-NH2/TCT/2-Amino-Py@Cu(OAc)2 as heterogeneous and porous catalyst.

All materials and solvents used in this work such as zirconium chloride (ZrCl4, Merck, 99%), 2-amino terephthalic acid (NH2-BDC, Merck, 95%), 2-amino-pyridine (Merck, 95%), 2,4,6-trichloro-1,3,5-triazine (TCT, Merck, 98%), Cu(CH3COO)2) Merck, 95%), N(Et)3) Merck), EtOH (Merck, 99%), ethyl cyanoacetate (Merck, 98%), acetonitrile (Merck, 99% ), p-toluene sulfonic acid (Merck, 98.5%), aldehyde derivatives (Merck), hydrazine (Merck, 80% in H2O), phenyl hydrazine (Merck, 97%) and N, N-dimethylformamide (DMF, Aldrich, 99%) were obtained from commercial sources without further purification.

Firstly, UiO-66-NH2 and UiO-66-NH2/TCT were synthesized according to the previously reports45. In a 50 mL round-bottom flask, UiO-66-NH2/TCT (0.5 g), 2-aminopyridine (7 mmol, 0.658 g), N(Et)3 (20 mol%, 0.02 g) and dry THF (25 mL) as a solvent were refluxed for 24 h. In the next step, solid mixture was separated by centrifuge (3000 rpm/min) and washed three times with ethanol and dried in a vacuum oven at 60 °C for 12 h46,47. In the following, in a 25 mL round-bottom flask, a mixture of UiO-66-NH2/TCT/2-amino-Py (0.5 g) and Cu(CH3COO)2 (0.2 mmol, 0.036 g) were stirred in ethanol (20 mL) as a solvent in room temperature for 2 h. Then, UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 was filtered using a centrifuge (3000 rpm/min) and dried under vacuum at 60 °C to grow a copper complex based on Zr-MOFs as a novel heterogeneous and porous catalyst (Fig. 5).

Synthesis Zr-MOFs based copper complex as a novel heterogeneous and porous catalyst.

The first, raw materials such as 3-(1H-indol-3-yl)-1-phenyl-1H-pyrazol-5-amine (1) and 3-(4-chlorophenyl)-1H-pyrazol-5-amine (2) were prepared according to the previously reported (Fig. 4)48,49,50,51,52. In the following, in a 10 mL round-bottomed flask, a mixture of aromatic aldehydes (1 mmol), ethyl cyanoacetate (1 mmol, 0.113 g) and (1) or/and(2) in percent of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 (15 mg) as catalyst were stirred under solvent-free condition at 110 °C. The progress and completion of the reaction was monitored by using TLC technique. Then the reaction mixture was allowed to cooled up to room temperature. The reaction mixture was dissolved in hot ethanol (20 mL) to separate the catalyst by using centrifugation (4000 rpm/min). The desired products (1a–12a) were washed with acetone/ethanol and collected by simple filtration and (1b–8b). Finally, the crude products were purified by column chromatography (Fig. 4).

Since the role of the anomeric effect can be found in the course of synthesis of various organic compounds53,54, herein, we decided to synthesize new compounds via an anomeric supporting mechanism. On the other hand, the importance of developing new catalysts for chemical reactions increased our motivation to produce new porous catalysts. Creating a copper complex based on metal–organic frameworks creates a new approach to the preparation of heterogeneous catalysts. The structure of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 as a porous and heterogeneous catalyst was completely identified using various techniques such as FT-IR, XRD, SEM, N2 adsorption–desorption isotherms (BET), BJH, EDS, SEM-elemental mapping, TG and DTG. The UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 was used for prepareing new pyrazolo[3,4-b]pyridine-5-carbonitriles. These compounds may be had biological and medicinal applications due to the presence of indole and pyrazole moieties. The structure of the synthesized compounds was confirmed using FT-IR, 1H-NMR, 13C-NMR and melting point techniques. This report describes all the experiments package, including the synthesis of catalyst, the optimization and mechanism of the reaction via anomeric-based oxidation pathway for the aromatization of the mentioned molecules under air and neutral atmosphere.

The FT-IR spectra of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 as a catalyst and starting materials were shown in Fig. 6. The two peaks at 3475 and 3357 cm−1 of NH2 functional groups are represented synthesis of UiO-66-NH245. Also, the absorption peaks at 2800–3000 cm−1 are related to aromatic C–H and C=C stretches bands. The addition of different compounds during the catalyst synthesis steps results in changes in the spectra that indicate a change in structure.

FT-IR spectra of catalyst and starting materials.

The XRD pattern of different stages of materials and catalyst synthesis was compared (Fig. 7). The XRD pattern of UiO-66-NH2 was identical to the previously reported data45. The last stage of copper complex based on Zr-MOFs has been proved by appearing of peaks. Also, below the peak at 2θ < 10, indicating the structure of the crystal plates of the various phases has suitable stability.

Comparison XRD pattern of (a) UiO-66-NH2, (b) UiO-66-NH2/TCT (c) UiO-66-NH2/TCT/2-amino-Py and (d) UiO-66-NH2/TCT/2-Amino-Py@Cu(OAc)2 a copper complex based on Zr-MOFs as a novel heterogeneous and porous catalyst.

The morphology of UiO-66-NH2 and UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 was also studied by scanning electron microscopy (SEM) technique (Fig. 8a). As shown in Fig. 8a, morphology of catalyst particles is tetrahedral which is in good condition and not completely stacked. Also, the morphology of UiO-66-NH2 is stable after post-modification. Elemental mapping analysis shows Zr, N, O, C and Cu atoms which were confirmed in the structure of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 (Fig. 8b). Furthermore, the well-dispersed distribution of elements in the UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 was determined and verified by elemental mapping analysis (Fig. 8b).

(a) Scanning electron microscope (SEM) images of UiO-66-NH2 (a,b) and UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 (c,d). (b) EDX spectroscopy and elemental mapping analysis of UiO-66-NH2/TCT/2-amino-Py@ Cu(OAc)2 a copper complex based on Zr-MOFs as a novel heterogeneous and porous catalyst.

In another searching, the textural properties of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 were studied by N2 adsorption–desorption isotherms (Fig. 9a). Based on the obtained results, the area calculated based on the BET equation, the total pore volume 115 m2 g−1 and 0.1523 cm3 g−1 respectively. The pore size distribution of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 based on BJH method is shown in (Fig. 9a). The mean pore diameter for the catalyst is 8.48 nm. The presence of a suitable surface area, as well as the size of catalyst cavities can be a major reason for the high efficiency at the synthesis of pyrazolo[3,4-b]pyridine-5-carbonitriles. The thermal gravimetric (TG) and derivative thermal gravimetric (DTG) analysis of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 was shown in Fig. 9b. According to this diagram, several failures due to the separation of the copper complex and organic compounds of Zr-MOFs are shown. The diagram shows that the synthesized catalyst is stable up to 240 °C.

(a) N2 adsorption–desorption isotherms and the pore size distribution of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2. (b) Thermal gravimetric (TG) and derivative thermal gravimetric (DTG) analysis of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 as a novel heterogeneous and porous catalyst.

After confirming the structure of a copper complex based on Zr-MOFs, we attempted to evaluate its catalytic performance for the synthesis of various new pyrazolo[3,4-b]pyridine-5-carbonitriles. For this purpose, we selected the reaction between 4-chloro-benzaldehyde (1 mmol, 0.140 g), ethyl cyanoacetate (1 mmol, 0.113 g) and 3-(4-chlorophenyl)-1H-pyrazol-5-amine (1 mmol, 0.193 g) as a model reaction. In order to select suitable conditions, the model of reaction was evaluated using various solvents, different temperatures and amounts of catalysts. The results are shown in Table 1. According to the presented data in Table 1, the best of choice for the synthesis of pyrazolo[3,4-b]pyridine-5-carbonitriles was achieved in percent of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 (15 mg) as catalyst under solvent-free conditions at 110 °C.

After selecting the optimal conditions for the synthesis of 3,4-bis(4-chlorophenyl)-6-oxo-6,7-dihydro-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile (1a), a wide range of aromatic aldehydes including electron withdrawing, electron releasing and heterocyclic rings were tested for obtaining of desired products (Fig. 10). As shown in Fig. 10, the obtained results indicated that UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 is appropriate for the preparation of target molecules in high to excellent yields (60–85%) with relatively short reaction times (90–120 min.).

Synthesis of pyrazolo[3,4-b]pyridine-5-carbonitriles using UiO-66-NH2/TCT/2-amino-Py@Cu a copper complex based on Zr-MOFs as a novel heterogeneous and porous catalyst.

To evaluate the performance of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 as a catalyst in comparison to those other catalysts for the preparation pyrazolo[3,4-b]pyridine-5-carbonitriles, we have used various homogeneous and heterogeneous catalysts and previous stages of the final catalyst for the condensation reaction 4-chloro-benzaldehyde (1 mmol, 0.140 g), ethyl cyanoacetate (1 mmol, 0.113 g) and 3-(4-chlorophenyl)-1H-pyrazol-5-amine (1 mmol, 0.193 g) as a model reaction in Table 2. As shown the obtained data in the Table 2, UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 is the best catalyst for the synthesis of pyrazolo[3,4-b]pyridine-5-carbonitrile derivatives.

Suggested mechanism for the synthesis of pyrazolo[3,4-b]pyridine-5-carbonitriles using UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 as a heterogeneous and porous catalyst was shown in Fig. 11. At the first step, ethyl cyanoacetate is converted to enolate form and react with activated aldehyde to produce intermediate (I) by losing one molecule of H2O. In the following, (3-(1H-indol-3-yl)-1-phenyl-1H-pyrazol-5-amine (1) and/or 3-(4-chlorophenyl)-1H-pyrazol-5-amine (2) attack to intermediate (I) as a Michael acceptor created intermediate (II). In the next step, intermediate (II) is converted to intermediate (III) through tautomerization and intramolecular cyclization. Finally, the intermediate (III) converts to their corresponding derivatives via a cooperative vinylogous anomeric based oxidation and releases one molecule of hydrogen (–H2) and/or hydrogen peroxide (–H2O2) molecules26,60,61. The obtained results of the reaction model under argon, nitrogen and oxygen atmospheres are similar which are verified the presented mechanism. The term cooperative is used when more than one lone pair of electrons and other donors are sharing the anti-bonding orbitals of one acceptor bond (nN → σ*C–H). The simultaneous cooperative sharing of electrons from donors into the anti-bonding orbitals of the C–H bond is a major driving force for hydride releasing (nN → σ*C–X).

The proposed mechanism for the synthesis of pyrazolo[3,4-b]pyridine-5-carbonitriles using UiO-66-NH2/TCT/2-Amino-Py@Cu(OAc)2.

To prove the recyclability of the presented catalyst, we tested model reaction under the optimal reaction conditions in the previously section. The results of Fig. 12a show that the UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 as a catalyst can be reused up to 4 times without noticeable changes in its catalytic activity. This performance indicates the high stability of the copper complex created on the Zr-MOFs as a heterogeneous and porous catalyst. To prove the stability of the catalyst structure, the recovered catalyst was evaluated by FT-IR and XRD analysis. The results are shown in Fig. 12b and c. According to the results, there have been not many changes in the catalyst structure, indicating the stability of the catalyst. Also, to investigate the heterogeneous nature of the protocols and Cu leaching, ICP results proved that no Zr and Cu leaching was detected in the filtrate (Zr: 2.41 × 10−6 and Cu: 2.03 × 10−5 mol/g respectively) upon reaction completion, which indicates the high stability of the prepared catalyst.

(a) Recyclability of catalyst for the synthesis of pyrazolo[3,4-b]pyridine-5-carbonitriles. Comparison (b) XRD, (c) FT-IR of reused and fresh catalyst.

In summary, Zr-MOFs based copper complex was introduced. At this catalyst, copper was supported on the surface of metal–organic frameworks as a new porous complex. Proper stability and morphology of the presented catalyst can create a new approach in the preparation of porous and heterogeneous catalysts. Catalytic performance of UiO-66-NH2/TCT/2-amino-Py@Cu(OAc)2 was demonstrated in the synthesis of new pyrazolo[3,4-b]pyridine-5-carbonitriles via anomeric based oxidation concept. These compounds can have biological and medicinal applications due to the presence of indole and pyrazole nucleus. High efficiency of products and gentle green conditions are other features of the products synthesized using this new porous and heterogeneous catalyst.

The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.

Millward, A. R. & Yaghi, O. M. Metal–organic frameworks with exceptionally high capacity for storage of carbon dioxide at room temperature. J. Am. Chem. Soc. 127, 17998–17999 (2005).

Article CAS PubMed Google Scholar

Kalmutzki, M. J., Diercks, C. S. & Yaghi, O. M. Metal–organic frameworks for water harvesting from air. Adv. Mater. 30, 1704304 (2018).

Article Google Scholar

Kitagawa, S. Metal–organic frameworks (MOFs). Chem. Soc. Rev. 43, 5415–5418 (2014).

Article PubMed Google Scholar

Masoomi, M. Y., Morsali, A., Dhakshinamoorthy, A. & Garcia, H. Mixed-metal MOFs: Unique opportunities in metal–organic framework (MOF) functionality and design. Angew. Chem. 131, 15330–15347 (2019).

Article ADS Google Scholar

Farrusseng, D., Aguado, S. & Pinel, C. Metal–organic frameworks: Opportunities for catalysis. Angew. Chem. Int. Ed. Engl. 48, 7502–7513 (2009).

Article CAS PubMed Google Scholar

Sepehrmansourie, H. Spotlight: Metal organic frameworks (MOFs): As multi-purpose catalysts. Iran. J. Catal. 11, 207–215 (2021).

CAS Google Scholar

Jiang, H. et al. Photocatalytic aldehydes/alcohols/toluenes oxidative amidation over bifunctional Pd/MOFs: Effect of Fe-O clusters and Lewis’s acid sites. J. Catal. 401, 279–287 (2021).

Article CAS Google Scholar

Ghasemzadeh, M. A., Mirhosseini-Eshkevari, B., Tavakoli, M. & Zamani, F. Metal–organic frameworks: Advanced tools for multicomponent reactions. Green Chem. 22, 7265–7300 (2020).

Article CAS Google Scholar

Sepehrmansourie, H., Zarei, M., Zolfigol, M. A., Babaee, S. & Rostamnia, S. Application of novel nanomagnetic metal–organic frameworks as a catalyst for the synthesis of new pyridines and 1,4-dihydropyridines via a cooperative vinylogous anomeric based oxidation. Sci. Rep. 11, 5279 (2021).

Article ADS CAS PubMed PubMed Central Google Scholar

Feng, X., Song, Y. & Lin, W. Dimensional reduction of Lewis acidic metal–organic frameworks for multicomponent reactions. J. Am. Chem. Soc. 143, 8184–8192 (2021).

Article CAS PubMed Google Scholar

Sepehrmansouri, H. et al. Multilinker phosphorous acid anchored En/MIL-100(Cr) as a novel nanoporous catalyst for the synthesis of new N-heterocyclic pyrimido [4,5-b] quinolines. Mol. Catal. 481, 110303 (2020).

Article CAS Google Scholar

Tavakoli, E. et al. Applications of novel composite UiO-66-NH2/melamine with phosphorous acid tags as a porous and efficient catalyst for the preparation of novel spiro-oxindoles. New J. Chem. 46, 19054–19061 (2022).

Article CAS Google Scholar

Kalhor, S. et al. Novel uric acid-based nano organocatalyst with phosphorous acid tags: Application for synthesis of new biologically-interest pyridines with indole moieties via a cooperative vinylogous anomeric based oxidation. Mol. Catal. 507, 111549 (2021).

Article CAS Google Scholar

Rasooll, M. M. et al. Novel nano-architectured carbon quantum dots (CQDs) with phosphorous acid tags as an efficient catalyst for the synthesis of multisubstituted 4H-pyran with indole moieties under mild conditions. RSC Adv. 11, 25995–26007 (2021).

Article ADS CAS PubMed PubMed Central Google Scholar

Babaee, S., Zarei, M., Sepehrmansourie, H., Zolfigol, M. A. & Rostamnia, S. Synthesis of metal–organic frameworks MIL-101(Cr)-NH2 containing phosphorous acid functional groups: Application for the synthesis of N-amino-2-pyridone and pyrano [2,3-c] pyrazole derivatives via a cooperative vinylogous anomeric-based oxidation. ACS Omega 5, 6240–6249 (2020).

Article CAS PubMed PubMed Central Google Scholar

Jalili, F., Zarei, M., Zolfigol, M. A., Rostamnia, S. & Moosavi-Zare, A. R. SBA-15/PrN(CH2PO3H2)2 as a novel and efficient mesoporous solid acid catalyst with phosphorous acid tags and its application on the synthesis of new pyrimido [4,5-b] quinolones and pyrido [2,3-d] pyrimidines via anomeric based oxidation. Microporous Mesoporous Mater. 294, 109865 (2020).

Article CAS Google Scholar

Zhong, M., Pannecoucke, X., Jubault, P. & Poisson, T. Recent advances in photocatalyzed reactions using well-defined copper (I) complexes. Beilstein J. Org. Chem. 16, 451–481 (2020).

Article CAS PubMed PubMed Central Google Scholar

Nasrollahzadeh, M., Motahharifar, N., Nezafat, Z. & Shokouhimehr, M. Copper (II) complex anchored on magnetic chitosan functionalized trichlorotriazine: An efficient heterogeneous catalyst for the synthesis of tetrazole derivatives. Colloids Interface Sci. Commun. 44, 100471 (2021).

Article CAS Google Scholar

Xia, J. et al. Mechanistic study of Ni and Cu dual catalyst for asymmetric C–C bond formation; asymmetric coupling of 1,3-dienes with C-nucleophiles to construct vicinal stereocenters. ACS Catal. 11, 6643–6655 (2021).

Article CAS Google Scholar

Qi, J., Wei, F., Tung, C. H. & Xu, Z. Modular synthesis of α-quaternary chiral β-lactams by a synergistic copper/palladium-catalyzed multicomponent reaction. Angew. Chem. Int. Ed. Engl. 60, 13814–13818 (2021).

Article CAS PubMed Google Scholar

Gawande, M. B. et al. Magnetically recyclable magnetite-ceria (Nanocat-Fe-Ce) nanocatalyst-applications in multicomponent reactions under benign conditions. Green Chem. 15, 1226–1231 (2013).

Article CAS Google Scholar

McGrath, K. P. & Hoveyda, A. H. A multicomponent Ni, Zr, and Cu-catalyzed strategy for enantioselective synthesis of alkenyl-substituted quaternary carbons. Angew. Chem. Int. Ed. Engl. 53, 1910–1914 (2014).

Article CAS PubMed PubMed Central Google Scholar

Jiang, B. et al. Four-component strategy for selective synthesis of azepino [5, 4, 3-cd] indoles and pyrazolo [3, 4-b] pyridines. Chem. Commun. 50, 6108–6111 (2014).

Article CAS Google Scholar

Torabi, M., Yarie, M., Zolfigol, M. A., Azizian, S. & Gu, Y. A magnetic porous organic polymer: Catalytic application in the synthesis of hybrid pyridines with indole, triazole and sulfonamide moieties. RSC Adv. 12, 8804–8814 (2022).

Article ADS CAS PubMed PubMed Central Google Scholar

Mohamed, L. W., Shaaban, M. A., Zaher, A. F., Alhamaky, S. M. & Elsahar, A. M. Synthesis of new pyrazoles and pyrozolo [3, 4-b] pyridines as anti-inflammatory agents by inhibition of COX-2 enzyme. Bioorg. Chem. 83, 47–52 (2019).

Article CAS PubMed Google Scholar

Torabi, M., Zolfigol, M. A., Yarie, M. & Gu, Y. Application of ammonium acetate as a dual rule reagent-catalyst in synthesis of new symmetrical terpyridines. Mol. Catal. 516, 111959 (2021).

Article CAS Google Scholar

Faria, J. V. et al. Recently reported biological activities of pyrazole compounds. Bioorg. Med. Chem. 25, 5891–5903 (2017).

Article CAS PubMed Google Scholar

Charris-Molina, A., Castillo, J. C., Macías, M. & Portilla, J. One-Step synthesis of fully functionalized pyrazolo [3, 4-b] pyridines via isobenzofuranone ring opening. J. Org. Chem. 82, 12674–12681 (2017).

Article CAS PubMed Google Scholar

Abnous, K. et al. In vitro evaluation of dihydropyridine-3-carbonitriles as potential cytotoxic agents through PIM-1 protein kinase inhibition. Res. Pharm. Sci. 12, 196 (2017).

Article PubMed PubMed Central Google Scholar

Amer, M. M., Aziz, M. A., Shehab, W. S., Abdellattif, M. H. & Mouneir, S. M. Recent advances in chemistry and pharmacological aspects of 2-pyridone scaffolds. J. Saudi Chem. Soc. 25, 101259 (2021).

Article CAS Google Scholar

Abdelaziz, M. E., El-Miligy, M. M., Fahmy, S. M., Mahran, M. A. & Hazzaa, A. A. Design, synthesis and docking study of pyridine and thieno [2, 3-b] pyridine derivatives as anticancer PIM-1 kinase inhibitors. Bioorg. Chem. 80, 674–692 (2018).

Article CAS PubMed Google Scholar

Ling, Y. et al. The expanding role of pyridine and dihydropyridine scaffolds in drug design. Drug Des. Dev. Ther. 15, 4289 (2021).

Article CAS Google Scholar

Alabugin, I. V. Stereoelectronic Effects: A Bridge Between Structure and Reactivity 1st edn. (Wiley, 2016).

Book Google Scholar

Alabugin, I. V. et al. Stereoelectronic power of oxygen in control of chemical reactivity: The anomeric effect is not alone. Chem. Soc. Rev. 50, 10253–10345 (2021).

Article CAS PubMed Google Scholar

Alabugin, V., Kuhn, L., Krivoshchapov, N. V., Mehaffy, P. & Medvedev, M. G. Anomeric effect, hyperconjugation and electrostatics: Lessons from complexity in a classic stereoelectronic phenomenon. Chem. Soc. Rev. 50, 10212–10252 (2021).

Article CAS PubMed Google Scholar

Juaristi, E. & Cuevas, G. Recent studies of the anomeric effect. Tetrahedron 48, 5019–5087 (1992).

Article CAS Google Scholar

Bai, C. B., Wang, N. X., Xing, Y. & Lan, X. W. Progress on chiral NAD(P)H model compounds. Synlett 28, 402–414 (2017).

CAS Google Scholar

He, T. et al. Base-promoted cascade approach for the preparation of reduced knoevenagel adducts using hantzsch esters as reducing agent in water. Synlett 27, 1864–1869 (2016).

Article CAS Google Scholar

Hamasaka, G., Tsuji, H. & Uozumi, Y. Organoborane-catalyzed hydrogenation of unactivated aldehydes with a Hantzsch ester as a synthetic NAD(P)H analogue. Synlett 26, 2037–2041 (2015).

Article CAS Google Scholar

Babaee, S., Zarei, M. & Zolfigol, M. A. MOF-Zn-NHC as an efficient N-heterocyclic carbene catalyst for aerobic oxidation of aldehydes to their corresponding carboxylic acids via a cooperative geminal anomeric based oxidation. RSC Adv. 11, 36230–36236 (2021).

Article ADS CAS PubMed PubMed Central Google Scholar

Sepehrmansourie, H., Zarei, M., Zolfigol, M. A. & Gu, Y. A new approach for the synthesis of bis (3-Indolyl) pyridines via a cooperative vinylogous anomeric based oxidation using ammonium acetate as a dual reagent-catalyst role under mild and green condition. Polycycl. Aromat. Compd. https://doi.org/10.1080/10406638.2022.2128830 (2022).

Article Google Scholar

Sepehrmansourie, H. et al. Catalytic synthesis of new pyrazolo [3, 4-b] pyridine via a cooperative vinylogous anomeric-based oxidation. Sci. Rep. 12, 14145 (2022).

Article ADS CAS PubMed PubMed Central Google Scholar

Ahmadi, H., Zarei, M. & Zolfigol, M. A. Catalytic application of a novel basic alkane-sulfonate metal–organic frameworks in the preparation of pyrido [2,3-d] pyrimidines via a cooperative vinylogous anomeric-based oxidation. ChemistrySelect 47, e202202155 (2022).

Article Google Scholar

Kalhor, S. et al. Anodic electrosynthesis of MIL-53(Al)-N(CH2PO3H2)2 as a mesoporous catalyst for synthesis of novel (N-methyl-pyrrol)-pyrazolo [3,4-b] pyridines via a cooperative vinylogous anomeric based oxidation. Sci. Rep. 11, 19370 (2021).

Article ADS CAS PubMed PubMed Central Google Scholar

Chen, M., Tu, Y. & Wu, S. Preparation of UiO-66-NH2@PDA under water system for chemical warfare agents degradation. Materials 14, 2419 (2021).

Article ADS CAS PubMed PubMed Central Google Scholar

Moghaddam, F. M., Jarahiyan, A., Heidarian Haris, M. & Pourjavadi, A. An advancement in the synthesis of nano Pd@magnetic amine-functionalized UiO-66-NH2 catalyst for cyanation and O-arylation reactions. Sci. Rep. 11, 11387 (2021).

Article ADS CAS PubMed PubMed Central Google Scholar

Sadeghi, S., Jafarzadeh, M., Abbasi, A. R. & Daasbjerg, K. Incorporation of CuO NPs into modified UiO-66-NH2 metal–organic frameworks (MOFs) with melamine for catalytic C–O coupling in the Ullmann condensation. New J. Chem. 41, 12014–12027 (2017).

Article CAS Google Scholar

Pandey, G. & Vaitla, J. Desulfonylative methenylation of β-keto sulfones. Org. Lett. 17, 4890–4893 (2015).

Article CAS PubMed Google Scholar

Sun, L., Bera, H. & Chui, W. K. Synthesis of pyrazolo [1, 5-a][1, 3, 5] triazine derivatives as inhibitors of thymidine phosphorylase. J. Med. Chem. 65, 1–11 (2013).

Article CAS Google Scholar

Afsar, J. et al. Synthesis and application of melamine-based nano catalyst with phosphonic acid tags in the synthesis of (3-indolyl) pyrazolo [3,4-b] pyridines via vinylogous anomeric based oxidation. Mol. Catal. 482, 110666 (2020).

Article CAS Google Scholar

Slaett, J., Romero, I. & Bergman, J. Cyanoacetylation of indoles, pyrroles and aromatic amines with the combination cyanoacetic acid and acetic anhydride. Synthesis 16, 2760–2765 (2004).

Google Scholar

Ahmad, I., Mishra, N. K. & Ghosh, T. 5-(1H-Indol-3-yl)-pyrazolyl derivatives as colorimetric sensor for anions. J. Incl. Phenom. Macrocycl. 76, 183–191 (2013).

Article CAS Google Scholar

Yarie, M. Catalytic anomeric based oxidation. Iran. J. Catal. 7, 85–88 (2017).

CAS Google Scholar

Yarie, M. Catalytic vinylogous anomeric based oxidation. Iran. J. Catal. 10, 79–83 (2020).

CAS Google Scholar

Zarei, M., Sepehrmansourie, H., Zolfigol, M. A., Karamian, R. & Farida, S. H. M. Novel nano-size and crab-like biological-based glycoluril with sulfonic acid tags as a reusable catalyst: Its application to the synthesis of new mono-and bis-spiropyrans and their in vitro biological studies. New J. Chem. 42, 14308–14317 (2018).

Article CAS Google Scholar

Sepehrmansourie, H., Zarei, M., Taghavi, R. & Zolfigol, M. A. Mesoporous ionically tagged cross-linked poly (vinyl imidazole) s as novel and reusable catalysts for the preparation of N-heterocycle spiropyrans. ACS Omega 4, 17379–17392 (2019).

Article CAS PubMed PubMed Central Google Scholar

Moosavi-Zare, A. R. et al. Design, characterization and application of new ionic liquid 1-sulfopyridinium chloride as an efficient catalyst for tandem Knoevenagel–Michael reaction of 3-methyl-1-phenyl-1H-pyrazol-5 (4H)-one with aldehydes. Appl. Catal. A Gen. 467, 61–68 (2013).

Article CAS Google Scholar

Zolfigol, M. A. Silica sulfuric acid/NaNO2 as a novel heterogeneous system for production of thionitrites and disulfides under mild conditions. Tetrahedron 57, 9509–9511 (2001).

Article CAS Google Scholar

Sepehrmansourie, H. Silica sulfuric acid (SSA): As a multipurpose catalyst. Iran. J. Catal. 10, 175–179 (2020).

CAS Google Scholar

Torabi, M. et al. Synthesis of triarylpyridines with sulfonate and sulfonamide moieties via a cooperative vinylogous anomeric-based oxidation. Sci. Rep. 11, 16846 (2021).

Article ADS CAS PubMed PubMed Central Google Scholar

Naseri, A. M. et al. Synthesis and application of [Zr-UiO-66-PDC-SO3H]Cl MOFs to the preparation of dicyanomethylene pyridines via chemical and electrochemical methods. Sci. Rep. 11, 16817 (2021).

Article ADS CAS PubMed PubMed Central Google Scholar

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We thank the Bu-Ali Sina University and Iran Science Elites Federation (INSF) for financial support.

Department of Organic Chemistry, Faculty of Chemistry, Bu-Ali-Sina University, Hamedan, 6517838965, Iran

Elham Tavakoli, Hassan Sepehrmansourie, Mohammad Ali Zolfigol & Ardeshir Khazaei

Department of Chemistry, Faculty of Science, University of Qom, Qom, 37185-359, Iran

Mahmoud Zarei

Department of Phytochemistry, Medicinal Plant and Drugs Research Institute, Shahid Beheshti University, Evin, Tehran, 1983963113, Iran

Mohammad Ali As’Habi

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E.T., and H.S.; methodology, validation, investigation. M.Z. investigation and writing the original draft. M.A.Z.; supervision, resources, project administration, funding acquisition, conceptualization, writing-review. A.K. supervision. M.A.A. Performing Mass-spectroscopy of synthesized products.

Correspondence to Mahmoud Zarei, Mohammad Ali Zolfigol or Ardeshir Khazaei.

The authors declare no competing interests.

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Tavakoli, E., Sepehrmansourie, H., Zarei, M. et al. Application of Zr-MOFs based copper complex in synthesis of pyrazolo[3, 4-b]pyridine-5-carbonitriles via anomeric-based oxidation. Sci Rep 13, 9388 (2023). https://doi.org/10.1038/s41598-023-34172-1

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Received: 04 January 2023

Accepted: 25 April 2023

Published: 09 June 2023

DOI: https://doi.org/10.1038/s41598-023-34172-1

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