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Discovery and Development of Metal-Catalyzed Coupling Reactions in the Synthesis of Dasabuvir, an HCV-Polymerase Inhibitor.

David M BarnesShashank ShekharTravis B DunnJufang H BarkalowVincent S ChanThaddeus S FranczykAnthony R HaightJohn E HengeveldLawrence KolaczkowskiBrian J KoteckiGuangxin LiangJames C MarekMaureen A McLaughlinDonna K MontavonJames J Napier
Published in: The Journal of organic chemistry (2019)
Dasabuvir (1) is an HCV polymerase inhibitor which has been developed as a part of a three-component direct-acting antiviral combination therapy. During the course of the development of the synthetic route, two novel coupling reactions were developed. First, the copper-catalyzed coupling of uracil with aryl iodides, employing picolinamide 16 as the ligand, was discovered. Later, the palladium-catalyzed sulfonamidation of aryl nonaflate 33 was developed, promoted by electron-rich palladium complexes, including the novel phosphine ligand, VincePhos (50). This made possible a convergent, highly efficient synthesis of dasabuvir that significantly reduced the mutagenic impurity burden of the process.
Keyphrases
  • hepatitis c virus
  • highly efficient
  • combination therapy
  • room temperature
  • human immunodeficiency virus
  • small molecule
  • electron transfer
  • high throughput
  • structural basis
  • reduced graphene oxide
  • electron microscopy