Synfacts 2011(3): 0240-0240  
DOI: 10.1055/s-0030-1259406
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag Stuttgart ˙ New York

Synthesis of an HCV RNA Polymerase Inhibitor

Contributor(s): Philip Kocienski
L.-C. Campeau*, P. D. O’Shea
Merck Frosst Canada, Kirkland, Canada
Further Information

Publication History

Publication Date:
16 February 2011 (online)

Significance

The target molecule, an HCV RNA polymerase (NS5B) inhibitor, was synthesized in twelve steps on a multigram scale (9% overall yield). The synthesis features the late-stage introduction of the 6-amino group in the 7-deazapurine moiety via a mild SNAr reaction using NaN3 (HI), followed by a chemoselective Staudinger reaction in the penultimate step.