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Paper ID:IJSREM63778

An Efficient synthesis of novel 8,8-dimethyl-2-(4- nitrophenyl)-5-phenyl-5,7,8,9-tetrahydro-6H- [1,3,4]thiadiazolo[2,3-b]quinazolin-6-one catalyzed by Cu(OAc) 2

Stream/Area:

-

Subject:

-

Paper ID:

IJSREM63778

Volume:

10 |

5 |

May 2026

Pages:

1-9

Publication Frequency:

Monthly (12 issues per year)

DOI
Digital Object Identifier
10.55041/IJSREM63778

License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.

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Authors

NR

N. Rama

Department of Chemistry

PRISM PG & DG College

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JN

J. Namrta

Department of Chemistry

PRISM PG & DG College

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D

D.Sudiir

Department of Chemistry

PRISM PG & DG College

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DN

Dr. N.Krishnarao

Department of Chemistry

PRISM PG & DG College

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Abstract

This study synthesized a novel series of 5-phenyl-5,7,8,9-tetrahydro-6H-[1,3,4] thiadiazolo [2,3-b]quinazolin-6-one using Cu(OAc)2 a novel catalyst. A one-pot multicomponent synthesis reaction involving dimedone, substituted aromatic aldehydes, and 5-(4-nitrophenyl)-1, 3, 4-thiadiazol-2-amine in the presence of ethanol as a solvent, which generated a variety of new thiadiazolo [2,3-b]quinazolin-6-one scaffolds. This component can be made by refluxing semithiocarbazide with 4-nitrobenzoic acid in the presence of ethanol and sulfuric acid. A low E-factor, high reaction mass efficiency, atom economy, scalability, and rapid reaction time are just a few of the notable benefits of this freshly discovered technology. In addition to invitro study of antimicrobial activity evaluated of titled derivatives..

KEYWORDS

KEYWORDS: 5-(4-nitrophenyl)-1 3 4-thiadiazol-2-amine dimedone substituted aryl aldehydes Cu (OAc)2

Cite This Article

N. Rama, J. Namrta, D.Sudiir, Dr. N.Krishnarao, "An Efficient synthesis of novel 8,8-dimethyl-2-(4- nitrophenyl)-5-phenyl-5,7,8,9-tetrahydro-6H- [1,3,4]thiadiazolo[2,3-b]quinazolin-6-one catalyzed by Cu(OAc) 2," International Journal of Scientific Research in Engineering and Management, vol. 10, no. 5, pp. 1-9, May 2026. https://doi.org/10.55041/IJSREM63778

Full Article/Conclusion

                To generate a series of thiadiazolo[2,3-b] quinazolin-6-ones, a one-pot, one-step, multicomponent reaction involving dimedone, substituted aromatic aldehydes, and 5-aryl-1,3,4-thiadiazol-2-amines in the presence of Cu(OAc)2 under solvent conditions like ethanol has been devised. This procedure is quick, simple, practical, and eco-friendly. High to exceptional yields, high reaction speeds, avoidance of hazardous organic solvents, simplicity of use, simple catalyst recycling and separation, appropriateness for large-scale synthetic applications, generation of water as green waste, and superior atom economy and the evaluation of  antimicrobial activity

References

1. Navin B. Patel,*, Rahul B. Parmar and Hetal I. Soni,” Lewis Acid Promoted, One-Pot Synthesis of Fluoroquinolone Clubbed 1,3,4-Thiadiazole Motifs under Microwave Irradiation: Their Biological Activities”, Current Microwave Chemistry, 2020, 7, 60-66. 2. Akhil A. Nagar*, Ashish Patel, Rajesh K.S , Kishore R. Danao , L.G. Rathi ,“Solvent Free One Pot Microwave Synthesis of Quinazolines 4-(3H)-One Derivatives with their Antibacterial and Antifungal Activity”,Pharmagene Vol: 1, Issue: 1 3.Yousry A. Ammar a, Sondos M.A. Abd El-Hafez b, Sadia A. Hessein b, Abeer M. Ali b, Ahmed A. Askar c, Ahmed Ragab,”One-pot strategy for thiazole tethered 7-ethoxy quinoline hybrids: Synthesis and potential antimicrobial agents as dihydrofolatereductase (DHFR) inhibitors with molecular docking study”,Journal of Molecular Structure,Volume 1242, 15 October 2021, 130748. 4.SunilL. Dhonnar a, VishnuA. Adole a, RajendraH. Patil b, Bhushan B. Khairnar c, Thansing B. Pawar a, Nutan V. Sadgir a, Bapu S. Jagdale” Synthesis, spectral, antifungal, in silico molecular docking, ADME and DFT studies of some 2-(2-hydrazineyl)thiazole derivatives: Computational and experimental perspective”,Journal of Molecular Structure, Volume 1294, Part 1, 15 December 2023, 136411. 5. Sagar Sahu, Tanesh Sahu, GunjanKalyani, and BinaGidwani,” Synthesis and Evaluation of Antimicrobial Activity of 1, 3, 4-Thiadiazole Analogues for Potential Scaffold”,J Pharma copuncture. 2021 Mar 31; 24(1): 32–40. 6.ZainabAmer* ,Entesar O. Al-Tamimi,” Synthesis and Characterization of New 1,3,4-Thiadiazole Derivatives Containing Azo Group from Acid Hydrazide and Studying Their Antioxidant Activity”, Chemical Methodologies 6(2022) 604-611. 7.ManjoorAhamad Syed1*, Yiragam Reddy Padmanabha Reddy2 , K. B. Chandrasekhar,”Design, One-pot Synthesis and Biological Evaluation of Imidazo[2,1-b] [1,3,4] Thiadiazole Derivatives for their Antitubercular and Anti-Fungal Activity”, Journal of Applied Pharmaceutical Science Vol. 8(07), pp 021-027, July, 2018. 8.Ashok K. Shakya et al ,” Synthesis of some new thiadiazole derivatives and their anticonvulsant activity,” Bulgarian Chemical Communications,2014, 46(4):750-756 9.Shashikant R Pattan et al ,” Synthesis of some new thiadiazole derivatives and their antidiabetic activity”, Indian Journal of Heterocyclic Chemistry ,  2008, 17(3). 10. ChiépiNadège Dominique Dou, Georges StéphaneDembele, Mamadou Guy-Richard Kone,” Design of New Thiadiazole Derivatives with Improved Antidiabetic Activity”, Computational Chemistry, 2023, 11, 67-80.

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Publication Date

5/22/2026

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Review Rounds: 2

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