Microwave assisted efficient synthesis of diphenyl substituted pyrazoles using PEG-600 as solvent - A green approach

被引:9
作者
Ganapathi, M. [1 ]
Jayaseelan, D. [2 ]
Guhanathan, S. [2 ]
机构
[1] Govt Arts Coll, PG & Res Dept Chem, Tiruvannamalai, Tamil Nadu, India
[2] Muthurangam Govt Arts Coll Autonomous, PG & Res Dept Chem, Vellore, Tamil Nadu, India
关键词
Chalcones; Pyrazole; Piperidine; Antimicrobial activity; PEG-600; Microwave irradiation (MWI); DERIVATIVES; CHALCONES; POTENT;
D O I
10.1016/j.ecoenv.2015.05.002
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A conventional and microwave assisted efficient synthesis of diphenyl substituted pyrazole using PEG 600 as green solvent has been described. A relatively shorter reaction time with excellent yield of the piperidine mediated protocol has been attracted economically attractive and eco-friendly. All newly synthesized compounds were characterized by standard spectroscopic techniques viz., UV-visible, FT-IR, H-1-NMR and Mass spectra. The anti-microbial activities of compounds have also been tested using Minimum Inhibitory Concentration (MIC) method with two different microorganisms Staphylococcus aureus (MTCC3381) and Escherichia coli (MTCC739). The results of the antimicrobial activity revealed that the diphenyl substituted pyrazole derivatives have nice inhibiting nature against both types of bacteria of present investigation than corresponding chalcones. Since, the work has been focused on green chemical approach towards the synthesis, this protocol may be recommended for eco-friendly applications. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:87 / 92
页数:6
相关论文
共 14 条
[1]   Synthesis of novel pyrazole derivatives and evaluation of their antidepressant and anticonvulsant activities [J].
Abdel-Aziz, Mohamed ;
Abuo-Rahma, Gamal El-Din A. ;
Hassan, Alaa A. .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2009, 44 (09) :3480-3487
[2]   Design, synthesis and biological investigation of certain pyrazole-3-carboxylic acid derivatives as novel carriers for nitric oxide [J].
Abdel-Hafez, El-Shimaa M. N. ;
Abuo-Rahma, Gamal El-Din A. A. ;
Abdel-Aziz, Mohamed ;
Radwan, Mohamed F. ;
Farag, Hassan H. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2009, 17 (11) :3829-3837
[3]  
Ali TES, 2009, EUR J MED CHEM, V44, P4385, DOI [10.1016/j.ejmech.2009.06.022, 10.1016/j.ejmech.2009.05.031]
[4]  
Bekhit A A, 2001, Boll Chim Farm, V140, P297
[5]   Synthesis and anti-inflammatory effect of chalcones and related compounds [J].
Hsieh, HK ;
Lee, TH ;
Wang, JP ;
Wang, JJ ;
Lin, CN .
PHARMACEUTICAL RESEARCH, 1998, 15 (01) :39-46
[6]   The impact of microwave synthesis on drug discovery [J].
Kappe, CO ;
Dallinger, D .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (01) :51-63
[7]   Rynaxypyr™:: A new insecticidal anthranilic diamide that acts as a potent and selective ryanodine receptor activator [J].
Lahm, George P. ;
Stevenson, Thomas M. ;
Selby, Thomas P. ;
Freudenberger, John H. ;
Cordova, Daniel ;
Flexner, Lindsey ;
Bellin, Cheryl A. ;
Dubas, Christine M. ;
Smith, Ben K. ;
Hughes, Kenneth A. ;
Hollingshaus, J. Gary ;
Clark, Christopher E. ;
Benner, Eric A. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2007, 17 (22) :6274-6279
[8]   Antimalarial alkoxylated and hydroxylated chalones: Structure-activity relationship analysis [J].
Liu, M ;
Wilairat, P ;
Go, ML .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (25) :4443-4452
[9]  
MURAKAMI S, 1991, BIOCHEM PHARMACOL, V42, P1447
[10]   ANTI-TUMORIGENIC CHALCONES [J].
SHIBATA, S .
STEM CELLS, 1994, 12 (01) :44-52