Molecules (Jul 2012)

A New Synthetic Route to Original Sulfonamide Derivatives in 2-Trichloromethylquinazoline Series: A Structure-Activity Relationship Study of Antiplasmodial Activity

  • Nadine Azas,
  • Sylvain Rault,
  • Pascal Rathelot,
  • Sébastien Hutter,
  • Aurélien Dumètre,
  • Charline Kieffer,
  • Anita Cohen,
  • Pierre Verhaeghe,
  • Nicolas Primas,
  • Patrice Vanelle

DOI
https://doi.org/10.3390/molecules17078105
Journal volume & issue
Vol. 17, no. 7
pp. 8105 – 8117

Abstract

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We report herein a simple and efficient two-step synthetic approach to new 2-trichloromethylquinazolines possessing a variously substituted sulfonamide group at position 4 used to prepare new quinazolines with antiparasitic properties. Thus, an original series of 20 derivatives was synthesized, which proved to be less-toxic than previously synthesized hits on the human HepG2 cell line, but did not display significant antiplasmodial activity. A brief Structure-Activity Relationship (SAR) evaluation shows that a more restricted conformational freedom is probably necessary for providing antiplasmodial activity.

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