PEG-600: Greensolvent for synthesis of pyrazolo[5,1-c]thieno[3,4-e][1,2,4]triazin-6-amine

2021 ◽  
Author(s):  
Srinivasa Reddy Bireddy ◽  
Venkata Ramana Reddy Chittireddy ◽  
Laxminarayana Eppakayala
Keyword(s):  
2020 ◽  
Vol 22 (40) ◽  
pp. 23226-23236
Author(s):  
Eris Sinoimeri ◽  
Victor Maia Fernandes ◽  
Jérôme Cognard ◽  
Jorge Fernando Brandão Pereira ◽  
Lenka Svecova ◽  
...  

Large amounts of Fe(iii) or Fe(ii) strongly modify the biphasic behavior of the system P44414Cl/HCl/H2O while large amounts of Fe(iii) induce a biphasic regime for the mixture PEG-600/HCl/H2O.


2011 ◽  
Vol 509 (3) ◽  
pp. 885-890 ◽  
Author(s):  
Guo-Ying Zhang ◽  
Yan-Yan Xu ◽  
Dong-Zhao Gao ◽  
Ya-Qiu Sun

1970 ◽  
Vol 2 (2) ◽  
pp. 76-80
Author(s):  
Tajnin Ahmed ◽  
Muhammad Shahidul Islam ◽  
Tasnuva Haque ◽  
Mohammad Abusyed

In the present study sustained release diclofenac sodium matrix tablets were prepared using Kollidon SR polymer. Hydroxypropyl methylcellulose (HPMC 15 cps) and poly ethylene glycol (PEG-600) polymers respectively were used in formulating tablets prepared by direct compression and wet granulation methods. The polymers were used to explore the release pattern of the drug into the dissolution media. The tablets were also prepared in various shapes (caplet oval, round oval and flat oval). A comparatively higher release rate of drug was obtained from the polymer HPMC 15 cps at 10% concentration for directly compressed matrix tablet than those containing 20% of HPMC after a definite period of time. In wet granulation process, 10% PEG-600 containing tablets showed a better release than those containing 20% PEG. The drug release was also found to be sustained in case of wet granulation method than that of the direct compression method. Again the caplet shaped tablets in case of direct compression method showed better release rate of drug than those of the round oval and flat oval shaped tablets. Thus the result of this study shows that the proper selection of the percentage of polymer and the suitable shape of tablet and proper manufacturing method can provide a greater opportunity in designing sustained release dosage forms. Key words: Matrix tablet; release pattern; direct compression; wet granulation; PEG 600; Kollidon SR.DOI: 10.3329/sjps.v2i2.5828Stamford Journal of Pharmaceutical Sciences Vol.2(2) 2009: 76-80


Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1294
Author(s):  
Sandeep T. Atkore ◽  
Giribala M. Bondle ◽  
Pranita V. Raithak ◽  
Vinod T. Kamble ◽  
Ravi Varala ◽  
...  

The synthesis of 14-aryl 14H-dibenzo[a,j]xanthenes is achieved by a simple condensation reaction between β-naphthol with aryl or alkyl aldehydes in an effective synergetic catalytic system created by combining basic bleaching earth clay and PEG-600. The advantages of the present method include catalyst recyclability, superior product yield, a shorter reaction time and the avoidance of hazardous reagents. Synthesized xanthene derivatives were also screened for their antibacterial activity against Staphylococcus aureus (MTCC 96) and Pseudomonas aeruginosa (Wild).


2019 ◽  
Vol 210 ◽  
pp. 627-635 ◽  
Author(s):  
Muhammad Rizwan Dilshad ◽  
Atif Islam ◽  
Usamah Hamidullah ◽  
Fahd Jamshaid ◽  
Adnan Ahmad ◽  
...  
Keyword(s):  

2021 ◽  
Vol 25 (7) ◽  
pp. 138-146
Author(s):  
E. Laxminarayana ◽  
P. Bhasker ◽  
D. Ramesh ◽  
Md. Rafeeq ◽  
B. Srinivasa Reddy

compound 2-((1H-benzo[d]imidazol-2-yl)thio)acetic acid (1) with o-aminobenzamide (2) gave compound (2-[1-(1H-benzimidazol-2-yl)-ethylsulfanyl]-3H-quinazolin-4-one (3). 3 could also be syntehsized by an alternative two routes scheme 2 and scheme 3. It appears from scheme 3 that it is giving good yields under green and eco-friendly conditions using PEG-600 (polyethylent glycol). Compound 10 was synthesized in two routes scheme4 and scheme 5. It appears from Route B (Scheme 4) that it is giving good yields: alkylation followed by oxidation in route A followed by alkylation in PEG-600 used as a green solvent. The total sequence of reactions has been carried out using eco-friendly and green conditions. Further, anticancer activity was carried out by using docking studies and binding conformation of active compounds of 3, 8, 9 and 10. The results show that 3 and 9 have potential to be developed as chemotherapeutic agents and compounds 3, 9 molecule showed best fit, potent dock score when compared with doxorubicin.


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