scholarly journals Eco-Friendly Novel Synthesis, Characterization of 2,3-Disubstituted 4-Thiazolidinone Derivatives and their Antimicrobial Evaluations

2021 ◽  
Vol 33 (11) ◽  
pp. 2685-2692
Author(s):  
Ashutosh Pathak ◽  
P. Malairajan ◽  
Parmesh Kumar Dwivedi ◽  
Devdutt Chaturvedi

A total of nine derivatives of 4-thiazolidinone were synthesized involving the reaction of benzene-1,2- diamine with 4-aminobenzoic acid followed by reaction with substituted benzaldehyde to get the Schiff bases. These synthesized Schiff bases were further reacted with thioglycolic acid to get the desired thiazolidinones (29-37). In addition to conventional synthesis, the microwave irradiation method has also been employedfor the synthesis of these compounds which provides not only pollution free and eco-friendly environment but also excellent yields. The results showed that 2-substituted thiazolidinone derivatives exhibit good antibacterial activity. It was also recorded that the compounds containing -Cl, -NO2 group with thiazolidinone nucleus are more active than other compounds of the synthesized series.

2018 ◽  
Vol 42 (10) ◽  
pp. 512-514
Author(s):  
Rui-bo Xu ◽  
Xiao-tian Yang ◽  
Hai-nan Li ◽  
Peng-cheng Zhao ◽  
Jiao-jiao Li ◽  
...  

Two new bis-Schiff bases containing a piperazine ring, N,N‘-bis(4-chlorobenzylidene)- and N,N‘-bis(4-cyanobenzylidene)-1,4-bis(3-aminopropyl)piperazine, were prepared by the reaction of N,N‘-bis(3-aminopropyl)piperazine with 4-chloro- and 4-cyanobenzaldehyde, respectively. The dichloro compound was fully identified by X-ray crystallography and it exhibited good antibacterial activity against Escherichia coli, Staphylococcus aureus and Bacillus subtilis.


Author(s):  
K Sunand ◽  
K Vinay Kumar ◽  
K Ashwini ◽  
P Suresh Kumar ◽  
S Vishnu ◽  
...  

Aim: To synthesize and evaluate 4-aminoantipyrine related schiff’s bases as antibacterial agents. Objective: To synthesize, purify, characterize and evaluate 4-aminoantipyrine. Method: Schiff bases derived from 4-aminoantipyrine play a vital role in biological and pharmacological activities. Knowing the importance of 4-aminoatipyrine schiff bases and their analogues wide varieties of bioactivities like analgesic, antiviral, antipyretic, anti-rheumatic, antimicrobial and anti-inflammatory activities have been widely studied. 4-aminoantipyrine compounds C1 (anisaldehyde), C2 (p-hydroxybenzaldehyde) and C3(vanillin) were prepared by condensation between 4-amino antipyrine and substituted aromatic benzaldehydes. The products were purified by recrystallization by using ethanol, characterized by IR spectroscopy. The N-H stretching in 4-aminoantipyrine is shown at 3430 cm-1 and -3325 cm-1. The -HC=N- stretching is observed in the range of 1508-1504 cm-1 The –OCH3 stretching is found at 1888 cm-1. 4-amino antipyrine related schiff’s bases evaluated their activity as antimicrobials in-vitro by spread plate method against E.coli. Schiff bases have potent antibacterial activity with gram negative bacteria E.coli. Results: Synthesis and characterization of a schiff bases derived from substituted benzaldehydes and 4-aminoantipyrine was evaluated and characterized with the IR spectroscopic techniques and schiff bases have shown potent antibacterial activity against E.Coli.


LWT ◽  
2019 ◽  
Vol 107 ◽  
pp. 89-97 ◽  
Author(s):  
Fei Liu ◽  
Haimei Wang ◽  
Songsong Cao ◽  
Chenggang Jiang ◽  
Juncai Hou

2012 ◽  
Vol 9 (2) ◽  
pp. 988-992
Author(s):  
Mukesh Kumar Ahirwar ◽  
S. P. Shrivastava

Some 4-thiazolidinone derivatives6(a-l)have been prepared bearing s-triazine moiety by the condensation of Schiff bases from bis-2,4 (4′-methyl-phenylamino)-s-triazine-6-ylaminobenzoyl substituted benzylhydrazone5(a-l)with thioglycolic acid. The structures of synthesized compound have been characterized by IR, 1HNMR spectral studies. The synthesized compounds6(a-l)has been screened for antibacterial activity.


2008 ◽  
Vol 181 (9) ◽  
pp. 2298-2305 ◽  
Author(s):  
Tingshun Jiang ◽  
Wei Shen ◽  
Qian Zhao ◽  
Mei Li ◽  
Jinyu Chu ◽  
...  

2013 ◽  
Vol 373 ◽  
pp. 53-58 ◽  
Author(s):  
Ting Hu ◽  
Chunxia Li ◽  
Xia Zhao ◽  
Guangsheng Li ◽  
Guangli Yu ◽  
...  

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