Abstract:In this paper, some new bis-acyl hydrazone derivatives (4a-f) were prepared through the reaction of carboxylic acid hydrazides with 1,4-diacetylbenzene using classical methods, microwave and ultrasound irradiation methods. These compounds are obtained through a series of reactions where some carboxylic acids react with ethanol first in the presence of concentrated sulfuric acid to give the corresponding esters (2a-f), which when treatment with aqueous hydrazine give carboxylic acid hydrazides (3a-f).thus, The … Show more
“…Looking at the diversified numerous applications of imines and thiazoles in varied fields of chemistry, there has always been attractive developments pertaining to greener, economical, efficient and feasible methods for their synthesis viz., in aqueous media [17,18]; using catalysts [19][20][21][22][23][24]; using Microwave Irridiation method [25,26]. In addition to all these findings; in this research paper, we herein report the green synthesis and anti-microbial evaluation of few thiazole-imino derivatives obtained from furfural imine and substituted acetophenone.…”
The ring forming reaction of furfural imine (A) and substituted acetophenone (B) via a greener approach resulted in the synthesis of thiazole-imino derivatives (C1 – C5). The compound A was synthesized by green method using acetic acid in aqueous media where conc. Sulfuric acid was avoided. The final compounds (C1-C5) were again synthesized in aqueous media avoiding use of organic solvents. The resultant compounds were characterized and distinguished from their precursors by elemental analysis, 1H-NMR, 13C-NMR and IR spectral studies. The in-vitro activities of the final compounds (C1-C5) depicted that they are all appreciably active against bacterial strains S. aureus, B. subtilis and fungal strains C. albicans, C. glabrata. Ciprofloxacin and Itraconazole were used as the control drugs for anti-bacterial and for anti-fungal activities; respectively. As compared to the other analogues, compound C2 (R = NO2) and C4 (R = Cl) showed best activities against the bacterial and fungal strains; respectively.
“…Looking at the diversified numerous applications of imines and thiazoles in varied fields of chemistry, there has always been attractive developments pertaining to greener, economical, efficient and feasible methods for their synthesis viz., in aqueous media [17,18]; using catalysts [19][20][21][22][23][24]; using Microwave Irridiation method [25,26]. In addition to all these findings; in this research paper, we herein report the green synthesis and anti-microbial evaluation of few thiazole-imino derivatives obtained from furfural imine and substituted acetophenone.…”
The ring forming reaction of furfural imine (A) and substituted acetophenone (B) via a greener approach resulted in the synthesis of thiazole-imino derivatives (C1 – C5). The compound A was synthesized by green method using acetic acid in aqueous media where conc. Sulfuric acid was avoided. The final compounds (C1-C5) were again synthesized in aqueous media avoiding use of organic solvents. The resultant compounds were characterized and distinguished from their precursors by elemental analysis, 1H-NMR, 13C-NMR and IR spectral studies. The in-vitro activities of the final compounds (C1-C5) depicted that they are all appreciably active against bacterial strains S. aureus, B. subtilis and fungal strains C. albicans, C. glabrata. Ciprofloxacin and Itraconazole were used as the control drugs for anti-bacterial and for anti-fungal activities; respectively. As compared to the other analogues, compound C2 (R = NO2) and C4 (R = Cl) showed best activities against the bacterial and fungal strains; respectively.
In this study, the synthesis of a few dihydrazide hydrazone molecules (A1-A6) employing a green chemistry strategy was accomplished successfully using straightforward, environmentally friendly methods. In a water bath sonicator, succinic dihydrazide (1 equivalent) and a variety of aldehydes (2 equivalents) were combined to quickly and efficiently synthesize the necessary compounds. The synthesized compounds were looked into and verified using IR, 1H-NMR, and 13C-NMR as well as physical properties. It's interesting to note that NMR data revealed that each produced chemical had many tautomeric isomers through proton transfer, as well as asymmetric structures. Actually, it is anticipated that the resultant compounds will have a great ability to form complexes with heavy metals, making them valuable in a variety of significant domains.
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