Green synthesis of pyrido[2,1‐ a ]isoquinolines and pyrido[1,2‐ a ]quinolins using Fe 3 O 4 ‐MNPs as efficient nanocatalyst: Study of antioxidant activity

Abstract In this work, synthesis of pyrido[2,1‐ a ]isoquinolines and pyrido[1,2‐ a ]quinolins in excellent yield using multicomponent reaction of phthalaldehyde, methyl amine, methyl malonyl chloride, alkyl bromides, and triphenylphosphine in the presence of catalytic amount of Fe 3 O 4 ‐MNPs with a...

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Published inJournal of heterocyclic chemistry Vol. 57; no. 1; pp. 337 - 345
Main Authors Faal Hamedani, Naghmeh, Ghazvini, Maryam, Azad, Leila, Noushin, Annataj
Format Journal Article
LanguageEnglish
Published 01.01.2020
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Summary:Abstract In this work, synthesis of pyrido[2,1‐ a ]isoquinolines and pyrido[1,2‐ a ]quinolins in excellent yield using multicomponent reaction of phthalaldehyde, methyl amine, methyl malonyl chloride, alkyl bromides, and triphenylphosphine in the presence of catalytic amount of Fe 3 O 4 ‐MNPs with aqueous sodium hydroxide at 80°C was investigated. The reduction of ferric chloride solution with Clover Leaf water extract caused to synthesis of magnetic iron oxide nanoparticles (Fe 3 O 4 ‐MNPs) as a green method. As well, antioxidant activity was studied for the some newly synthesized compounds such as 6a , 6c , 9b , and 9c using the DPPH radical trapping and reducing of ferric ion experiments and comparing results with synthetic antioxidants (TBHQ and BHT). As a result, compounds 6a , 6c , 9b , and 9c show good DPPH radical trapping and excellent reducing strength of ferric ion.
ISSN:0022-152X
1943-5193
DOI:10.1002/jhet.3782