Synthesis of vaniprevir (MK-7009): lactamization to prepare a 20-membered [corrected] macrocycle |
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Authors: | Song Zhiguo J Tellers David M Journet Michel Kuethe Jeffrey T Lieberman David Humphrey Guy Zhang Fei Peng Zhihui Waters Marjorie S Zewge Daniel Nolting Andrew Zhao Dalian Reamer Robert A Dormer Peter G Belyk Kevin M Davies Ian W Devine Paul N Tschaen David M |
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Affiliation: | Department of Process Chemistry, Merck Research Laboratories, P.O. Box 2000, Rahway, New Jersey 07065, United States. zhiguo_song@merck.com |
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Abstract: | Development of a practical synthesis of MK-7009, a 20-membered [corrected] macrocycle, is described. A variety of ring-closing strategies were evaluated, including ring-closing metathesis, intermolecular palladium-catalyzed cross-couplings, and macrolactamization. Ring closure via macrolactamization was found to give the highest yields under relatively high reaction concentrations. Optimization of the ring formation step and the synthesis of key intermediates en route to MK-7009 are reported. |
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