Design, Synthesis, and Structure-Activity Relationship of New Pyrimidinamine Derivatives Containing an Aryloxy Pyridine Moiety

J Agric Food Chem. 2017 Feb 15;65(6):1272-1280. doi: 10.1021/acs.jafc.6b05580. Epub 2017 Feb 6.

Abstract

The pyrimidinamine diflumetorim is an ideal template for the discovery of agrochemical lead compounds due to its unique mode of action, novel chemical structure, and lack of reported resistance. To develop a new pyrimidinamine fungicide effective against cucumber downy mildew (CDM), a series of new pyrimidinamine derivatives containing an aryloxy pyridine moiety were designed and synthesized by employing the recently reported intermediate derivatization method (IDM). The structures of all compounds were identified by 1H NMR, elemental analyses, HRMS, and X-ray diffraction. Bioassays demonstrated that some of the title compounds exhibited excellent fungicidal activities against CDM. Compound 9 gave the best activity (EC50 = 0.19 mg/L), which is significantly better than the commercial fungicides diflumetorim, flumorph, and cyazofamid. The relationship between structure and fungicidal activity of the synthesized pyrimidinamines was explored. The study showed that compound 9 is a promising fungicide candidate for further development.

Keywords: cucumber downy mildew; fungicidal activities; intermediate derivatization method (IDM); structure−activity relationship.

MeSH terms

  • Chemistry Techniques, Synthetic
  • Cucumis sativus / drug effects
  • Cucumis sativus / microbiology
  • Drug Design
  • Drug Evaluation, Preclinical
  • Fungicides, Industrial / chemical synthesis
  • Fungicides, Industrial / chemistry*
  • Fungicides, Industrial / pharmacology*
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Oomycetes / pathogenicity
  • Plant Diseases / microbiology
  • Pyridines / chemistry*
  • Structure-Activity Relationship*
  • X-Ray Diffraction

Substances

  • Fungicides, Industrial
  • Pyridines