Design and fabrication of a novel, recoverable, and heterogeneous magnetic composite based on Melamine-Functionalized SBA-15 for catalytic synthesis of Quinazoline compounds
Bibliographic record
Abstract
No abstract is available for this record. The assistant can identify its topic from the title, but cannot infer the study’s results.
Source: Not provided · Quality: missing
Research context
OpenAlex topics: Quinazolinone synthesis and applications · Microwave-Assisted Synthesis and Applications · Multicomponent Synthesis of Heterocycles
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (60)
Show source-provided references
1. R.S. Rohokale, U.A. Kshirsagar, Advanced synthetic strategies for constructing quinazolinone scaffolds. Synthesis 48(09), 1253–1268 (2016)10.1055/s-0035-1560413 ↗
2. S. Gatadi, T.V. Lakshmi, S. Nanduri, 4 (3H)-quinazolinone derivatives: promising antibacterial drug leads. Eur. J. Med. Chem. 170, 157–172 (2019)10.1016/j.ejmech.2019.03.018 ↗
3. D.H. Vu et al., Design, synthesis, anti-inflammatory evaluation, and molecular docking studies of novel quinazoline-4 (3H)-one-2-carbothioamide derivatives. RSC Adv. 15(4), 2850–2861 (2025)10.1039/D4RA09094B ↗
4. J. Sun et al., Design, synthesis and antitumor activity of FAK/PLK1 dual inhibitors with quinazolinone as the skeleton. Chem. Biodivers. 20(4), e202300146 (2023)10.1002/cbdv.202300146 ↗
5. Z. Wang et al., Design, synthesis and antiviral activity of novel quinazolinones. Eur. J. Med. Chem. 53, 275–282 (2012)10.1016/j.ejmech.2012.04.010 ↗
6. M. Ashraf-Uz-Zaman et al., Quinazolinone compounds have potent antiviral activity against Zika and dengue virus. J. Med. Chem. 66(15), 10746–10760 (2023)10.1021/acs.jmedchem.3c00924 ↗
7. G.W. Seifu et al., Synthesis, antimalarial, antileishmanial evaluation, and molecular docking study of some 3-aryl-2-styryl substituted-4 (3 H)-quinazolinone derivatives. BMC Chem. 16(1), 107 (2022)10.1186/s13065-022-00903-0 ↗
8. C.Y. Cheah, N.H. Fowler, Idelalisib in the management of lymphoma. Blood 128(3), 331–336 (2016)10.1182/blood-2016-02-702761 ↗
9. F.V. Costa et al., Hemodynamic and humoral effects of chronic antihypertensive treatment with fenquizone: importance of aldosterone response. J. Clin. Pharmacol. 30(3), 254–261 (1990)10.1002/j.1552-4604.1990.tb03469.x ↗
10. K.H. Olesen, B. Dupont, E. Flensted-Jensen, The combined diuretic action of Quinethazone and Furosemide in congestive heart failure: a permutation trial test. Acta Med. Scand. 187(1–6), 33–40 (1970)10.1111/j.0954-6820.1970.tb02903.x ↗
11. Z. Xing et al., Recent advances in quinazolinones as an emerging molecular platform for luminescent materials and bioimaging. Org. Chem. Front. 8(8), 1867–1889 (2021)10.1039/D0QO01425G ↗
12. D.R. Patel, K.C. Patel, Synthesis of some new thermally stable reactive dyes having 4 (3 H)-quinazolinone molecule for the dyeing of silk, wool, and cotton fibers. Fibers Polym. 12(6), 741–752 (2011)10.1007/s12221-011-0741-9 ↗
13. N. Yan, C. You, M. Cai, A practical synthesis of quinazolinones via intermolecular cyclization between 2-halobenzamides and benzylamines catalyzed by copper (I) immobilized on MCM-41. J. Organomet. Chem. 897, 161–169 (2019)10.1016/j.jorganchem.2019.07.003 ↗
14. J.-J. Zhong et al., Efficient acceptorless photo-dehydrogenation of alcohols and N-heterocycles with binuclear platinum (II) diphosphite complexes. Chem. Sci. 10(18), 4883–4889 (2019)10.1039/C8SC05600E ↗
15. X. Zhang et al., Direct synthesis of quinazolinones via the carbon-supported acid-catalyzed cascade reaction of isatoic anhydrides with amides and aldehydes. Tetrahedron Lett. 66, 152835 (2021)10.1016/j.tetlet.2021.152835 ↗
16. A.R. Desai, K.R. Desai, Niementowski reaction: microwave induced and conventional synthesis of quinazolinones and 3-methyl-1H-5-pyrazolones and their antimicrobial activity. Arkivoc 8, 98–108 (2005)10.3998/ark.5550190.0006.d09 ↗
17. B. Majumdar et al., One-pot magnetic iron oxide–carbon nanodot composite-catalyzed cyclooxidative aqueous tandem synthesis of quinazolinones in the presence of tert-butyl hydroperoxide. ACS Omega 3(10), 13711–13719 (2018)10.1021/acsomega.8b01794 ↗
18. H. Hou et al., Electrochemical synthesis of quinazolinone via I 2-catalyzed tandem oxidation in aqueous solution. RSC Adv. 11(29), 17721–17726 (2021)10.1039/D1RA02706A ↗
19. R.M. Hassan et al., Design and synthesis of new Quinazolinone derivatives: investigation of antimicrobial and biofilm Inhibition effects. Mol. Diversity, 2024: pp. 1–2210.1007/s11030-024-10830-y ↗
20. S. Sahoo, S. Pal, Copper-catalyzed one-pot synthesis of quinazolinones from 2-nitrobenzaldehydes with aldehydes: application toward the synthesis of natural products. J. Org. Chem. 86(24), 18067–18080 (2021)10.1021/acs.joc.1c02343 ↗
21. B.C. Roy et al., Tandem synthesis of quinazolinone scaffolds from 2-aminobenzonitriles using aliphatic alcohol–water system. Catal. Sci. Technol. 9(21), 6002–6006 (2019)10.1039/C9CY01094G ↗
22. A. Dutta et al., Sustainable parts-per‐million level catalysis with feiii: one‐pot cascade synthesis of 2, 3‐dihydroquinazolin‐4 (1H)‐ones in water. Appl. Organomet. Chem. 35(3), e6116 (2021)10.1002/aoc.6116 ↗
23. Y. Chen et al., Thiamine hydrochloride (VB1) as an efficient promoter for the one-pot synthesis of 2, 3-dihydroquinazolin-4 (1H)-ones. Tetrahedron Letters, 2012. 53(44): pp. 5923–592510.1016/j.tetlet.2012.08.090 ↗
24. A. Taguchi, F. Schüth, Ordered mesoporous materials in catalysis. Microporous Mesoporous Mater. 77(1), 1–45 (2005)10.1016/j.micromeso.2004.06.030 ↗
25. V. Chaudhary, S. Sharma, An overview of ordered mesoporous material SBA-15: synthesis, functionalization and application in oxidation reactions. J. Porous Mater. 24, 741–749 (2017)10.1007/s10934-016-0311-z ↗
26. D. Zhao et al., Triblock copolymer syntheses of mesoporous silica with periodic 50 to 300 Angstrom pores. Science. 279(5350), 548–552 (1998)10.1126/science.279.5350.548 ↗
27. S. Jarmolińska, A. Feliczak-Guzik, I. Nowak, Synthesis, characterization and use of mesoporous silicas of the following types SBA-1, SBA-2, HMM-1 and HMM-2. Materials. 13(19), 4385 (2020)10.3390/ma13194385 ↗
28. A. Sayari, B.-H. Han, Y. Yang, Simple synthesis route to monodispersed SBA-15 silica rods. J. Am. Chem. Soc. 126(44), 14348–14349 (2004)10.1021/ja0478734 ↗
29. P. Verma et al., Functionalized mesoporous SBA-15 silica: recent trends and catalytic applications. Nanoscale. 12(21), 11333–11363 (2020)10.1039/D0NR00732C ↗
30. B. Castanheira et al., Functionalized mesoporous silicas SBA-15 for heterogeneous photocatalysis towards CECs removal from secondary urban wastewater. Chemosphere. 287, 132023 (2022)10.1016/j.chemosphere.2021.132023 ↗
31. P. García-Acevedo et al., Simple thermal treatment to improve the MRI and magnetic hyperthermia performance of hybrid iron oxide-mesoporous silica nanocarriers. J. Mol. Liq. 398, 124299 (2024)10.1016/j.molliq.2024.124299 ↗
32. M.C. Bruzzoniti et al., Functionalized SBA-15 mesoporous silica in ion chromatography of alkali, alkaline earths, ammonium and transition metal ions. J. Chromatogr. A 1216(29), 5540–5547 (2009)10.1016/j.chroma.2009.05.052 ↗
33. X. Wang et al., Preparation of ordered large pore SBA-15 silica functionalized with aminopropyl groups through one-pot synthesis. Chem. Commun., 2004(23): pp. 2762–276310.1039/b408022j ↗
34. K.N. Koo et al., Preparation and characterization of superparamagnetic magnetite (Fe3O4) nanoparticles: a short review. Malays. J. Fundam. Appl. Sci. 15(1), 23–31 (2019)10.11113/mjfas.v15n2019.1224 ↗
35. S.M. Patil, Novel silica-coated magnetic nanoparticles and their synthetic applications. Iran. J. Catal., 2023. 13(4)
36. M. Abboud et al., Superparamagnetic Fe3O4 nanoparticles, synthesis and surface modification. Mater. Sci. Semicond. Process. 39, 641–648 (2015)10.1016/j.mssp.2015.05.035 ↗
37. M. Liu et al., Recent advances of magnetite (Fe3O4)-based magnetic materials in catalytic applications. Magnetochemistry. 9(4), 110 (2023)10.3390/magnetochemistry9040110 ↗
38. S.M. Patil, Recent advances of functionalized Fe3O4 as nanocatalyst in carbon-carbon coupling reaction: a review. Iran. J. Catal. 14(4), 1–14 (2024)
39. R. Tandon, N. Tandon, S.M. Patil, Overview on magnetically recyclable ferrite nanoparticles: synthesis and their applications in coupling and multicomponent reactions. RSC Adv. 11(47), 29333–29353 (2021)10.1039/D1RA03874E ↗
40. R. Tandon et al., Magnetically recyclable silica-coated magnetite-molybdate nanocatalyst and its applications in N-formylation reactions under solvent-free conditions. Lett. Org. Chem. 19(8), 616–626 (2022)10.2174/1570178619666220112112901 ↗
41. S. Patil, R. Tandon, N. Tandon, Synthesis and characterization of Fe3O4@ SiO2@ K10 NPs applicable for N-ter-butyloxycarbonylation using solvent-free conditions. in Journal of Physics: Conference Series. 2022. IOP Publishing10.1088/1742-6596/2267/1/012107 ↗
42. N. Tandon et al., Magnetically recyclable silica-coated ferrite magnetite-K 10 montmorillonite nanocatalyst and its applications in O, N, and S-acylation reaction under solvent-free conditions. RSC Adv. 11(35), 21291–21300 (2021)10.1039/D1RA02222A ↗
43. K.B. İşcan, B. Erdem, Synthesis and application of dual-functional sorbent SBA-15-Fe3O4-PDA-ODA for removing both water soluble and insoluble pollutants. Mater. Chem. Phys. 320, 129422 (2024)10.1016/j.matchemphys.2024.129422 ↗
44. F. Hassanzadeh-Afruzi et al., Guanidinylated SBA-15/Fe3O4 mesoporous nanocomposite as an efficient catalyst for the synthesis of pyranopyrazole derivatives. Sci. Rep. 11(1), 19852 (2021)10.1038/s41598-021-99120-3 ↗
45. E.M. Björk, Synthesizing and characterizing mesoporous silica SBA-15: a hands-on laboratory experiment for undergraduates using various instrumental techniques. J. Chem. Educ. 94(1), 91–94 (2017)10.1021/acs.jchemed.5b01033 ↗
46. F. Hassanzadeh-Afruzi et al., Facile synthesis of pyrazolopyridine pharmaceuticals under mild conditions using an algin-functionalized silica-based magnetic nanocatalyst (Alg@ SBA-15/Fe 3 O 4). RSC advances, 2023. 13(15): pp. 10367–1037810.1039/D2RA07228A ↗
47. T.-H. Liou, G.-W. Chen, S. Yang, Preparation of amino-functionalized mesoporous SBA-15 nanoparticles and the improved adsorption of tannic acid in wastewater. Nanomaterials 12(5), 791 (2022)10.3390/nano12050791 ↗
48. J. Mondal, T. Sen, A. Bhaumik, Fe 3 O 4@ mesoporous SBA-15: a robust and magnetically recoverable catalyst for one-pot synthesis of 3, 4-dihydropyrimidin-2 (1 H)-ones via the Biginelli reaction. Dalton Trans. 41(20), 6173–6181 (2012)10.1039/c2dt30106g ↗
49. M.M. Salehi et al., Highly efficient remediation of Chlorpyrifos and malachite green by an SBA-15 incorporated Guar gum-grafted-poly (acrylic acid)/cobalt ferrite matrix for water purification. Arab. J. Chem. 17(5), 105751 (2024)10.1016/j.arabjc.2024.105751 ↗
50. Q. Cheng et al., Conducting polypyrrole confined in ordered mesoporous silica SBA-15 channels: preparation and its electrorheology. Microporous Mesoporous Mater. 93(1–3), 263–269 (2006)10.1016/j.micromeso.2006.03.005 ↗
51. A. Fedorchuk et al., Synthesis, thermal evolution and magnetic investigations of SBA-15 silica functionalized with anchored iron phosphonate molecules. Nanotechnology 34(41), 415602 (2023).10.1088/1361-6528/ace059 ↗
52. F. Hassanzadeh-Afruzi et al., Efficient removal of Pb (II)/Cu (II) from aqueous samples by a guanidine-functionalized SBA-15/Fe3O4. Sep. Purif. Technol. 291, 120956 (2022)10.1016/j.seppur.2022.120956 ↗
53. Z. Amiri-Khamakani et al., Methyl alginate/santa Barbara amorphous-15/iron oxide nanocomposite for efficient removal of different pollutants from aquatic environments. Carbohydrate Polymer Technologies and Applications 8, 100562 (2024)10.1016/j.carpta.2024.100562 ↗
54. C.M. Simonescu et al., Novel magnetic nanocomposites based on carboxyl-functionalized SBA-15 silica for effective dye adsorption from aqueous solutions. Nanomaterials. 12(13), 2247 (2022)10.3390/nano12132247 ↗
55. S.J. Wu et al., Efficient one-pot synthesis of 2, 3-dihydroquinazoline-4 (1 H)-ones promoted by FeCl 3/neutral Al 2 O 3. Research on Chemical Intermediates, 2019. 45: pp. 2327–233910.1007/s11164-018-03732-w ↗
56. N. Nikooei, M.G. Dekamin, E. Valiey, Benzene-1, 3, 5-tricarboxylic acid-functionalized MCM-41 as a novel and recoverable hybrid catalyst for expeditious and efficient synthesis of 2, 3-dihydroquinazolin-4 (1 H)-ones via one-pot three-component reaction. Res. Chem. Intermed. 46(8), 3891–3909 (2020)10.1007/s11164-020-04179-8 ↗
57. F. Havasi, A. Ghorbani-Choghamarani, F. Nikpour, Synthesis and characterization of nickel complex anchored onto MCM-41 as a novel and reusable nanocatalyst for the efficient synthesis of 2, 3-dihydroquinazolin-4 (1H)-ones. Microporous and Mesoporous Materials, 2016. 224: pp. 26–3510.1016/j.micromeso.2015.10.036 ↗
58. J. Zhang et al., CuO nanoparticles catalyzed simple and efficient synthesis of 2, 3-dihydroquinazolin-4 (1H)-ones and quinazolin-4 (3H)-ones under ultrasound irradiation in aqueous ethanol under ultrasound irradiation in aqueous ethanol. Tetrahedron. 70(34), 5274–5282 (2014)10.1016/j.tet.2014.05.059 ↗
59. S. Santra et al., Nano-indium oxide: an efficient catalyst for one-pot synthesis of 2, 3-dihydroquinazolin-4 (1H)-ones with a greener prospect. Catal. Commun. 49, 52–57 (2014)10.1016/j.catcom.2014.01.032 ↗
60. T. Ghosh et al., Potassium tert-butoxide promoted synthesis of dihydroquinazolinones. J. Org. Chem. 86(21), 14695–14704 (2021)10.1021/acs.joc.1c01510 ↗