Green Synthetic Approach: An Efficient Eco-Friendly Tool for Synthesis of Biologically Active Oxadiazole Derivatives

被引:35
作者
Banik, Bimal Krishna [1 ]
Sahoo, Biswa Mohan [2 ]
Kumar, Bera Venkata Varaha Ravi [2 ]
Panda, Krishna Chandra [2 ]
Jena, Jasma [2 ]
Mahapatra, Manoj Kumar [3 ]
Borah, Preetismita [4 ]
机构
[1] Prince Mohammad Bin Fahd Univ, Coll Sci & Human Studies, Dept Math & Nat Sci, Al Khobar 31952, Saudi Arabia
[2] Biju Patnaik Univ Technol, Nodal Ctr Res, Roland Inst Pharmaceut Sci, Berhampur 760010, India
[3] Kanak Manjari Inst Pharmaceut Sci, Rourkela 769015, India
[4] CSIR, Cent Sci Instruments Org, Chandigarh 160030, India
关键词
drug; green chemistry; microwave; oxadiazole; synthesis; biological activities;
D O I
10.3390/molecules26041163
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Green synthetic protocol refers to the development of processes for the sustainable production of chemicals and materials. For the synthesis of various biologically active compounds, energy-efficient and environmentally benign processes are applied, such as microwave irradiation technology, ultrasound-mediated synthesis, photo-catalysis (ultraviolet, visible and infrared irradiation), molecular sieving, grinding and milling techniques, etc. Thesemethods are considered sustainable technology and become valuable green protocol to synthesize new drug molecules as theyprovidenumerous benefits over conventional synthetic methods.Based on this concept, oxadiazole derivatives are synthesized under microwave irradiation technique to reduce the formation of byproduct so that the product yield can be increased quantitatively in less reaction time. Hence, the synthesis of drug molecules under microwave irradiation follows a green chemistry approach that employs a set of principles to minimize or remove the utilization and production of hazardous toxic materials during the design, manufacture and application of chemical substances.This approach plays a major role in controlling environmental pollution by utilizing safer solvents, catalysts, suitable reaction conditions and thereby increases the atom economy and energy efficiency. Oxadiazole is a five-membered heterocyclic compound that possesses one oxygen and two nitrogen atoms in the ring system.Oxadiazole moiety is drawing considerable interest for the development of new drug candidates with potential therapeutic activities including antibacterial, antifungal, antiviral, anticonvulsant, anticancer, antimalarial, antitubercular, anti-asthmatic, antidepressant, antidiabetic, antioxidant, antiparkinsonian, analgesic and antiinflammatory, etc. This review focuses on different synthetic approaches of oxadiazole derivatives under microwave heating method and study of their various biological activities.
引用
收藏
页数:23
相关论文
共 78 条
[1]   Microwave-assisted efficient, one-pot, three-component synthesis of 3,5-disubstituted 1,2,4-oxadiazoles under solvent-free conditions [J].
Adib, M ;
Jahromi, AH ;
Tavoosi, N ;
Mahdavi, M ;
Bijanzadeh, HR .
TETRAHEDRON LETTERS, 2006, 47 (17) :2965-2967
[2]   Green Chemistry: Principles and Practice [J].
Anastas, Paul ;
Eghbali, Nicolas .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (01) :301-312
[3]  
Bala S., 2010, J PHARM RES, V3, P2993
[4]   Microwave-Assisted Rapid and Efficient Synthesis of New Series of Chromene-Based 1,2,4-Oxadiazole Derivatives and Evaluation of Antibacterial Activity with Molecular Docking Investigation [J].
Baral, Nilofar ;
Mohapatra, Seetaram ;
Raiguru, Bishnu Prasad ;
Mishra, Nilima Priyadarsini ;
Panda, Pravati ;
Nayak, Sabita ;
Pandey, Satyendra Kumar ;
Kumar, P. Sudhir ;
Sahoo, Chita Ranjan .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 2019, 56 (02) :552-565
[5]   The first one-pot ambient-temperature synthesis of 1,2,4-oxadiazoles from amidoximes and carboxylic acid esters [J].
Baykov, Sergey ;
Sharonova, Tatyana ;
Shetnev, Anton ;
Rozhkov, Sergey ;
Kalinin, Stanislav ;
Smirnov, Alexey V. .
TETRAHEDRON, 2017, 73 (07) :945-951
[6]   Groundbreaking Anticancer Activity of Highly Diversified Oxadiazole Scaffolds [J].
Benassi, Alessandra ;
Doria, Filippo ;
Pirota, Valentina .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (22)
[7]  
Bhandari M., 2017, Int. J. Pharm. Pharmaceut. Sci., V9, P10
[8]  
Bhansali S. G., 2015, PHARM CHEM, V7, P156
[9]  
Bharatiya N, 2014, IND J APPL RES, V4, P88
[10]  
Bhardwaj S., 2011, ACHIEVES APP SCI RES, V3, P558