SYNTHESIS AND SOME TRANSFORMATIONS OF HETEROCYCLIC SUBSTITUTED DERIVATIVES OF THIOGLYCOLICACID

2020 ◽  
Vol 54 (2 (252)) ◽  
pp. 93-98
Author(s):  
M.A. Samvelyan ◽  
T.V. Ghochikyan

The methods have been developed for the preparation of diheterocyclic systems of a new structure, such as pyrazolo- and 1,3,4-oxadiazolo-1,2,4-triazoles, based on S-substituted thioglycolic acid derivatives.

2012 ◽  
Vol 77 (1) ◽  
pp. 17-26 ◽  
Author(s):  
Ritu Sharma ◽  
Pushkal Samadhiya ◽  
Savitri Srivastava ◽  
Santosh Srivastava

A new series of N-[3-(10H-phenothiazinyl)-propyl]-2-(substituted phenyl)-4-oxo-5-( substituted benzylidene)-1,3-thiazolidine-carboxamide, 5(as) have been synthesized. The cycloaddition reaction of thioglycolic acid with N-[3-(10H-phenothiazinyl)-propyl]-N?-[(substituted phenyl)-methylidene]- urea, 3(a-s) in the presence of anhydrous ZnCl2 afforded new heterocyclic compounds N-[3-(10H-phenothiazinyl)-propyl]-2-(substituted phenyl)-4-oxo- 1,3-thiazolidine-carboxamide, 4(a-s). The later product on treatment with several selected substituted aromatic aldehydes in the presence of C2H5ONa undergoes Knoevenagel reaction to yield 5(a-s). The structure of compounds 1, 2, 3(a-s), 4(a-s) and 5(a-s) were confirmed by IR, 1H NMR, 13C NMR, Fmass and chemical analysis. All above compounds were screened for their antimicrobial activity against some selected bacteria and fungi and for antituberculosis activity compounds have been screened against the bacterium M. tuberculosis.


2016 ◽  
Vol 258 ◽  
pp. S290-S291
Author(s):  
A.V. Kasabova ◽  
M. Kondeva Burdina ◽  
J. Mitkov ◽  
M. Georgieva ◽  
V. Tzankova ◽  
...  

1986 ◽  
Vol 17 (13) ◽  
Author(s):  
A. R. BURILOV ◽  
M. A. PUDOVIK ◽  
L. N. USMANOVA ◽  
A. N. PUDOVIK

RSC Advances ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 556-564 ◽  
Author(s):  
Leila Zare Fekri ◽  
Hooshang Hamidian ◽  
Masoomeh Abdollahi Chekosarani

Urazolium diacetate catalyzed synthesis of new derivatives of 1,3-thiazolidine-4-ones (azo dispersive dyes family) via multicomponent reaction of various aldehydes, thioglycolic acid and 4-aminoazobenzene under solvent-free reaction was reported.


2021 ◽  
Vol 17 ◽  
Author(s):  
Leila Zare Fekri

Background: Thiazolidinone-4-ones belong to an important heterocyclic compounds because of their broad spectrum of biological activities. Several methods for the synthesis of 4-thiazolidinones were reported in the literature. The main synthetic routes to synthesize 1,3-thiazolidin-4-ones is the three component reaction between amine, a carbonyl compound and a mercapto-acid. Objective: Dapsone-Cu supported on silica coated Fe3O4 (Fe3O4@SiO2-pr@dapsone-Cu) as a new heterogeneous nanoparticle catalyst was synthesized and the structure and morphology of this catalyst were characterized by Fourier transform infrared spectroscopy (FT-IR), Xray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), zeta potential, vibrating sample magnetometry (VSM) and thermal gravimetric analysis (TGA). The new synthesized catalyst was applied as an effective nanocatalyst for the synthesis of new derivatives of azo-linked thiazolidinones through one-pot multi-component reaction of various aromatic aldehydes, thioglycolic acid and 4-aminoazobenzene under solvent-free condition. Methods: A mixture of aldehyde, thioglycolic acid, 4-aminoazobenzene (1 mmol) and 0.05 g Fe3O4@SiO2@dapsone-Cu MNPs were stirred at room temperature under solvent-free condition. Results: We report a facile, green, new and efficient method for the synthesis of thiazolidine-4-ones through three component reaction of various aldehydes, thioglycolic acid and 4-aminoazobenzene in the presence of Fe3O4@SiO2-propyl@dapsone-Cu complex under solvent-free reaction. Conclusion: This new procedure has the notable advantages such as excellent yields, short reaction time, operational simplicity, easy work-up, eco-friendly and using a non-toxic catalyst. Also, the catalyst is easily recoverable in the presence of an enourmous magnet and reused for six consecutive reaction cycles without significant loss of activity.


2018 ◽  
Vol 42 (2) ◽  
pp. 155-170
Author(s):  
Sunil Makwane ◽  
SD Srivastava ◽  
Rajiv Dua ◽  
SK Srivastava

A new series of 5-benzylidene-3-(5-ethyl-[1,3,4]thiadiazol-2-yl)-2-phenyl-thiazolidin-4-ones (3a-3m) were synthesized. The reaction of thioglycolic acid with benzylidene-(5-ethyl-[1,3,4] thiadiazol-2-yl)-amine 1a in the presence of anhydrous ZnCl2 afforded the new heterocyclic compounds 5-benzylidene-3-(5-ethyl-[1,3,4] thiadiazole-yl)-2-phenyl-thiazolidin-4-one, 2a. The latter product on treatment with several selected substituted aromatic aldehydes in the presence of sodium ethoxide underwent the Knoevenagel reaction to yield 5-benzylidene-3-(5-ethyl-[1,3,4] thiadiazol-2-yl)-2-phenyl-thiazolidin-4-ones, 3a-3m. The structures of the compounds were confirmed by IR, 1H-NMR, 13C-NMR and mass spectroscopy and by chemical analysis. All the above compounds were screened for their antimicrobial activity against some selected bacteria and fungi such as E. coli, B. Subtilis, and S. Typhi bacteria and A.niger, A. Flavus and F. oxisporium Fungi. Journal of Bangladesh Academy of Sciences, Vol. 42, No. 2, 155-170, 2018


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.


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