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Synthesis of a New 4-(Pyridin-3-yl)pyrimidine Derivatives for Anticancer Activity

  • Jung, Se-Jin (Life Sciences Research Division, Korea Institute of Science and Technology) ;
  • El-Deeb, Ibrahim Mustafa (Department of Biomolecular Science, University of Science and Technology) ;
  • Lee, So-Ha (Life Sciences Research Division, Korea Institute of Science and Technology)
  • 발행 : 2009.03.30

초록

This study is focused on the synthesis of urea and amide derivatives particularly, since the amide moiety is an essential binding group at the binding site. Urea derivatives 3-7 and 13-14 were obtained by reaction of 2-aminopyrimidines and other amines with diverse isocyanates in pyridine as a solvent under reflux. The urea derivatives were obtained in low yield because of the highly electron deficient nature of the amino group of the 2-aminopyrimidine. Amide derivatives 8-10 were obtained in moderate yields by reaction of compound 1 with aryl chloride derivatives. Also, arylamine 11 was synthesized by Buchwald-Hartwig amination in moderate yields. Most of the compound did not show good activity against A375P melanoma cells, compared with Sorafenib as control compound.

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참고문헌

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