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Ecofriendly Synthesis and Characterization of Glucoside Derivatives and Its Biological Evaluation

Nilesh B. Jadhav1 , Pawan P. Kalbende2 , Sandip B. Chaudhari3 , Ramesh T. Parihar4

Section:Research Paper, Product Type: Journal-Paper
Vol.11 , Issue.2 , pp.11-18, Apr-2024


Online published on Apr 30, 2024


Copyright © Nilesh B. Jadhav, Pawan P. Kalbende, Sandip B. Chaudhari, Ramesh T. Parihar . This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
 

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IEEE Style Citation: Nilesh B. Jadhav, Pawan P. Kalbende, Sandip B. Chaudhari, Ramesh T. Parihar, “Ecofriendly Synthesis and Characterization of Glucoside Derivatives and Its Biological Evaluation,” International Journal of Scientific Research in Chemical Sciences, Vol.11, Issue.2, pp.11-18, 2024.

MLA Style Citation: Nilesh B. Jadhav, Pawan P. Kalbende, Sandip B. Chaudhari, Ramesh T. Parihar "Ecofriendly Synthesis and Characterization of Glucoside Derivatives and Its Biological Evaluation." International Journal of Scientific Research in Chemical Sciences 11.2 (2024): 11-18.

APA Style Citation: Nilesh B. Jadhav, Pawan P. Kalbende, Sandip B. Chaudhari, Ramesh T. Parihar, (2024). Ecofriendly Synthesis and Characterization of Glucoside Derivatives and Its Biological Evaluation. International Journal of Scientific Research in Chemical Sciences, 11(2), 11-18.

BibTex Style Citation:
@article{Jadhav_2024,
author = {Nilesh B. Jadhav, Pawan P. Kalbende, Sandip B. Chaudhari, Ramesh T. Parihar},
title = {Ecofriendly Synthesis and Characterization of Glucoside Derivatives and Its Biological Evaluation},
journal = {International Journal of Scientific Research in Chemical Sciences},
issue_date = {4 2024},
volume = {11},
Issue = {2},
month = {4},
year = {2024},
issn = {2347-2693},
pages = {11-18},
url = {https://www.isroset.org/journal/IJSRCS/full_paper_view.php?paper_id=3492},
publisher = {IJCSE, Indore, INDIA},
}

RIS Style Citation:
TY - JOUR
UR - https://www.isroset.org/journal/IJSRCS/full_paper_view.php?paper_id=3492
TI - Ecofriendly Synthesis and Characterization of Glucoside Derivatives and Its Biological Evaluation
T2 - International Journal of Scientific Research in Chemical Sciences
AU - Nilesh B. Jadhav, Pawan P. Kalbende, Sandip B. Chaudhari, Ramesh T. Parihar
PY - 2024
DA - 2024/04/30
PB - IJCSE, Indore, INDIA
SP - 11-18
IS - 2
VL - 11
SN - 2347-2693
ER -

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Abstract :
Ethyl 2-imino-6-methyl-4-substituted phenyl-1, 2, 3, 4-tetrahydropyrimidine-5-carboxylate compounds [4a-g] were achieved via a one pot multicomponent reaction of ethyl acetoacetate, substituted aromatic aldehyde with guanidine. The reaction is efficiently endorsed to give the preferred products in high yields and in a moderately short time. The resulted pyrimidine derivatives [4a-g] were treated with 2, 3, 4, 6-tetra-O-acetyl-?-D-glucopyranosyl bromide, potassium hydroxide mixed into 1 gm of neutral alumina in solvent free microwave condition furnished a (2S, 3S, 4R, 5S)-2-(acetoxymethyl)-6-((5-(ethoxycarbonyl)-4-methyl-6-phenyl-1, 6-dihydropyrimidin-2-yl)amino) tetrahydro-2H-pyran-3,4,5-triyl triacetate [5a-g]. The resulted products be deacetylated using methanol and ammonia furnished a Ethyl 6- (substituted phenyl) -4- methyl -2- (((3S, 4R, 5R, 6S)-3, 4, 5-trihydroxy -6- (hydroxyl methyl) tetra hydro-2H-pyran-2-yl) amino)-1,6-dihydropyrimidine-5-carboxylate[6a-g]. The molecular structures of the novel synthesized compounds were revealed based on their spectral analysis and elemental analysis. The purity of all synthesized compounds was resoluted by TLC. In addition, preferred derivatives of the products were screened for antimicrobial activity and there in vitro antioxidant activity. The antioxidant activity of the resulted products was also examined and most of them exhibited potent activity.

Key-Words / Index Term :
Guanidine, Pyrimidine, Glucoside, antimicrobial activity, antifungal activity, antioxidant activity.

References :
[1] Huang, Zhibin, et al., "Efficient one-pot three-component synthesis of fused pyridine derivatives in ionic liquid," ACS Combinatorial Science, Vol. 13, Issue. 1, pp. 45-49, 2011.
[2] Arora, Neha, Surendra Nath Pandeya, "Synthesis and analgesic activity of novel pyrimidine derivatives," Synthesis, Vol. 11, Issue. 1, pp. 0-10, 2011.
[3] S?czewski, Franciszek, ?ukasz Balewski, "Biological activities of guanidine compounds, 2008–2012 update," Expert opinion on therapeutic patents, Vol. 23, Issue. 8, pp. 965-995, 2013.
[4] Rawat, B. Singh, S. C. Mehra, and Roopali Tandon, "Synthesis and antimicrobial activity of some new heterocyclic guanidine derivatives," World Journal of pharmacy and pharmaceutical sciences, Vol. 5, Issue. 9, pp. 1325-1337, 2016.
[5] Mohana, N. Kikkeri, N. Basavapatna, P. Kumar, and L. Mallesha, "Synthesis and biological activity of some pyrimidine derivatives," Drug invention today, Vol. 5, Issue. 3, pp. 216-222, 2013.
[6] Kumar, Arun, S. Sinha, and M.S. Chauhan, "Syntheses of novel antimycobacterial combinatorial libraries of structurally diverse substituted pyrimidines by three-component solid-phase reactions," Bioorganic & medicinal chemistry letters, Vol. 12, Issue. 4, pp. 667-669, 2002.
[7] Baraldi, P. Giovanni, et al., "Antimicrobial and antitumor activity of N-heteroimmine-1, 2, 3-dithiazoles and their transformation in triazolo-, imidazo-, and pyrazolopirimidines," Bioorganic & medicinal chemistry, Vol. 10, Issue. 2, pp. 449-456, 2002.
[8] Nasr, N. Magda, M. M. Gineinah, "Pyrido [2, 3?d] pyrimidines and Pyrimido [5?, 4?: 5, 6] pyrido [2, 3?d] pyrimidines as new antiviral agents: Synthesis and Biological Activity," An International Journal Pharmaceutical and Medicinal Chemistry, Vol. 335, Issue. 6, pp. 289-295, 2002.
[9] Sondhi, M.Sham, et al, "Anticancer, anti-inflammatory and analgesic activity evaluation of heterocyclic compounds synthesized by the reaction of 4-isothiocyanato-4-methylpentan-2-one with substituted o-phenylenediamines, o-diaminopyridine and (un) substituted o.," Australian Journal of Chemistry, Vol. 54, Issue. 1, pp. 69-74, 2001.
[10] Gangjee, Aleem et al, "Synthesis, antifolate, and antitumor activities of classical and nonclassical 2-amino-4-oxo-5-substituted-pyrrolo [2, 3-d] pyrimidines," Journal of medicinal chemistry, Vol. 44, Issue. 12, pp.1993-2003, 2001.
[11] Kumar, Neeraj, G. Singh, A. K. Yadav, "Synthesis of some new pyrido [2,3?d] pyrimidines and their ribofuranosides as possible antimicrobial agents," An International Journal of Main Group Elements, Vol.12, Issue. 1, pp. 52-56, 2001.
[12] Hosseinzadeh, Hossein, M. Nassiri Asl, "Anticonvulsant, sedative and muscle relaxant effects of carbenoxolone in mice," BMC pharmacology, Vol. 3, pp.1-6, 2003.
[13] Shih, Mei-Hsiu, Fang-Ying Ke., "Syntheses and evaluation of antioxidant activity of sydnonyl substituted thiazolidinone and thiazoline derivatives," Bioorganic & medicinal chemistry, Vol. 12, Issue 17, pp. 4633-4643, 2004.
[14] Sun, Xian-Yu, et al., "Synthesis and anti-inflammatory activity evaluation of some novel 6-alkoxy (phenoxy)-[1, 2, 4] triazolo [3, 4-a] phthalazine-3-amine derivatives," European journal of medicinal chemistry, Vol. 45, Issue. 11, pp. 4807-4812, 2010.
[15] Castel-Branco, M. M., et al., "The maximal electroshock seizure (MES) model in the preclinical assessment of potential new antiepileptic drugs," Methods and findings in experimental and clinical pharmacology, Vol. 31, Issue. 2, pp. 101-106, 2009.
[16] W. Ishioka, S. Oonuki, T. Iwadate, K. Nih, “Resorcinol alkyl glucosides as potent tyrosinase inhibitors,” Biorg Med Chem Lett, Vol. 29, pp. 313–316, 2019.
[17] Chen D, Chen R, Xie K, Duan Y, Dai J, “Production of acetophenone C-glucosides using an engineered C-glycosyl transferase in Escherichia coli,” Tetrahedron Lett, Vol. 59, pp. 1875–1878, 2018.
[18] Yamaguchi T, Takamura H, Matoba T, Terao J., “Bioscience, biotechnology, and biochemistry,” Vol. 62, pp.1201-1209, 1998.
[19] Jorgensen J. H. And Turnidge, “Susceptibility Test methods: Dilution and Disk diffusion methods,” In Manual of clinical Microbiology, Vol.2), Ed. Pfaller M. A., pp. 1152-1173, 2007.
[20] Abdelkhalek, A. Abdelfattah, et al., "Derivatives of Cucurbitacin-E-glucoside produced by Curvularia lunata NRRL 2178: anti-inflammatory, antipyretic, antitumor activities, and effect on biochemical parameters," Future Journal of Pharmaceutical Sciences, Vol. 3, Issue. 2, pp. 124-130, 2017.
[21] Qiu, Yan, et al., "Benzofuran ?-caprolactam glucosides, amides and phenylpropanoid derivatives with anti-inflammatory activity from Oxybaphus himalaicus," Phytochemistry, Vol. 191, pp. 112905, 2021.
[22] Peytam, Fariba, et al., "Imidazo [1, 2-c] quinazolines as a novel and potent scaffold of ?-glucosidase inhibitors: design, synthesis, biological evaluations, and in silico studies," Scientific Reports, Vol.13, Issue. 1, pp.15672, 2023.
[23] Hasan, Hiba Ali, A. Salman, E. Abdulmalek, "Anticancer activity and high content screening of new 6-substituted-5, 6-dihydrobenzo [4, 5] imidazo [1, 2-c] quinazoline derivatives," Research Journal of Pharmacy and Technology, Vol.14, Issue. 5, pp. 2397-2405, 2021.
[24] Jadhavar, S.Pradeep, et al., "Benzimidazoquinazolines as new potent anti-TB chemotypes: Design, synthesis, and biological evaluation," Bioorganic Chemistry, Vol. 99, pp. 103774, 2020.
[25] Li, Jun-cai, et al., "Design, synthesis and antifungal activity evaluation of isocryptolepine derivatives," Bioorganic Chemistry, Vol. 92, pp. 103266, 2019.
[26] Hasan, Hiba Ali, et al., "Synthesis of novel 6-substituted-5, 6-Dihydrobenzo [4, 5] Imidazo [1, 2-c] quinazoline compounds and evaluation of their properties," Journal of Molecular Structure, Vol. 1193, pp. 482-494, 2019.
[27] Hasan, Hiba Ali, et al., "Microwave synthesis, crystal structure, antioxidant, and antimicrobial study of new 6-heptyl-5, 6-dihydrobenzo [4, 5] imidazo [1, 2-c] quinazoline compound," Chemistry Central Journal, Vol. 12, Issue. 1, pp.1-15, 2018.
[28] Domány, György, et al., "Imidazo [1, 2-c] quinazolines with lipid peroxidation inhibitory effect," European journal of medicinal chemistry, Vol.33, Issue. 3, pp. 181-187, 1998.
[29] J.K. Wangui, D. Onyancha, et al., “Determination of tannin content in banana (Musa spp) midribs: a comparative study,” International Journal of Scientific Research in Chemical Sciences, Vol.10, Issue.1, pp.01-07, 2023.
[30] H. Nasser, N. Ali, R. Salamah, A. Deeb, “Determination of the optimal conditions to produce lovastatin compound from the fungus (Penicillium digitatum),” International Journal of Scientific Research in Chemical Sciences, Vol.10, issue. 3, pp.25-28, 2023.

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