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Ecofriendly synthesis of pyrano[2,3‐ d ]pyrimidine derivatives and related heterocycles with anti‐inflammatory activities
Author(s) -
AbdElAzim Mohamed H. M.,
Aziz Maged A.,
Mouneir Samar M.,
ELFarargy Ahmed F.,
Shehab Wesam S.
Publication year - 2020
Publication title -
archiv der pharmazie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.468
H-Index - 61
eISSN - 1521-4184
pISSN - 0365-6233
DOI - 10.1002/ardp.202000084
Subject(s) - malononitrile , pyrimidine , chemistry , catalysis , thiobarbituric acid , condensation , combinatorial chemistry , organic chemistry , condensation reaction , stereochemistry , antioxidant , physics , thermodynamics , lipid peroxidation
A versatile, efficient, clean, and facile method was used for the synthesis of pyrano[2,3‐ d ]pyrimidine derivatives by the one‐pot three‐component condensation reaction of thiobarbituric acid and malononitrile with p ‐chlorobenzaldehyde, using Fe 3 O 4 or ZnO or Mn 3 O 4 as nanostructure catalysts. The catalyst could be easily recovered using an external magnet and reused for six cycles with almost a consistent activity. A series of polyheterocyclic compounds containing five and/or six rings fused with each other was designed. The anti‐inflammatory activities for some of the newly synthesized compounds were evaluated. All the synthesized compounds were characterized on the basis of their elemental analyses and spectral data.