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Synfacts 2011(3): 0240-0240
DOI: 10.1055/s-0030-1259406
DOI: 10.1055/s-0030-1259406
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag
Stuttgart ˙ New YorkSynthesis of an HCV RNA Polymerase Inhibitor
L.-C. Campeau*, P. D. O’Shea
Merck Frosst Canada, Kirkland, Canada
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
16. Februar 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 (H → I), followed by a chemoselective Staudinger reaction in the penultimate step.