Synthesis of Some New Tetracyclic Pyrimidine Derivatives Using Exocyclic α,β-Unsaturated Ketone and Evaluation of Their Antitumor Activities

Journal Title: JOURNAL OF ADVANCES IN CHEMISTRY - Year 2013, Vol 4, Issue 1

Abstract

Thiazolopyrimidine 2 was obtained from the reaction of dihydropyrimidinone with chloroacetic acid and benzaldehyde. Thiazolopyrimidine 2 containing an α,β-unsaturated ketonic function [-CH=CH-CO-] has been used as a component of Michael addition with an equimolar amount of dinucleophiles to give a series of novel tetracyclic pyrimidine derivatives. Treatment of thiazolopyrimidine 2 with uracil, aminotriazole, cyanoacetic acid hydrazide, o-phenylenediamine or diaminopyridine afforded the corresponding pyridopyrimidine, triazolopyrimidine, pyrazolone, benzodiazepine and triazepine derivative, respectively. The detailed synthesis, spectroscopic data, and antitumor activity for synthesized compounds were reported.

Authors and Affiliations

Kamelia El-Mahdy

Keywords

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  • EP ID EP652553
  • DOI 10.24297/jac.v4i1.960
  • Views 172
  • Downloads 0

How To Cite

Kamelia El-Mahdy (2013). Synthesis of Some New Tetracyclic Pyrimidine Derivatives Using Exocyclic α,β-Unsaturated Ketone and Evaluation of Their Antitumor Activities. JOURNAL OF ADVANCES IN CHEMISTRY, 4(1), 311-317. https://europub.co.uk./articles/-A-652553