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Production of benzazepine derivatives via four-component reaction of isatins: study of antioxidant activity
- Source :
- Molecular Diversity. 25:2171-2182
- Publication Year :
- 2020
- Publisher :
- Springer Science and Business Media LLC, 2020.
-
Abstract
- In current research, benzazepine derivative is synthesized via a new process of four-component reaction of isatin or its derivatives, α-haloketones, activated acetylenic compounds, isoquinoline and potassium fluoride/clinoptilolite nanoparticles (KF/CP NPs) in acidic solution of H2O2 in water at room temperature. Also, antioxidation property of some prepared benzazepines is investigated by employing trapping diphenyl-picrylhydrazine (DPPH) radical and ability of ferric reduction experiment. Among investigated compounds, compounds 5c have good results relative to BHT and TBHQ as standard antioxidant. Also, the Gram-positive and Gram-negative bacteria disk diffusion research is used for the confirmation of antimicrobial power of some prepared benzazepines. The achieved outcomes of disk diffusion experiment showed that these compounds avoided the growth of bacteria. Our procedure has a few benefits relative to reported method such as good rate of reaction, product with high efficiency, simple removal of catalyst from mixture of reaction. In the yield of the product, KF/clinoptilolite nanoparticles show a satisfactory recyclable activity.
- Subjects :
- Isatin
Benzazepines
010402 general chemistry
01 natural sciences
Antioxidants
Catalysis
Benzazepine
Inorganic Chemistry
Reaction rate
chemistry.chemical_compound
Drug Discovery
medicine
Physical and Theoretical Chemistry
Isoquinoline
Molecular Biology
010405 organic chemistry
Organic Chemistry
General Medicine
Potassium fluoride
0104 chemical sciences
chemistry
Yield (chemistry)
Ferric
Information Systems
medicine.drug
Nuclear chemistry
Subjects
Details
- ISSN :
- 1573501X and 13811991
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- Molecular Diversity
- Accession number :
- edsair.doi.dedup.....2ba6cdecbe332c4d3035872aa03d70d7
- Full Text :
- https://doi.org/10.1007/s11030-020-10110-5