Practical Asymmetric Synthesis of Efavirenz (DMP 266), an HIV-1 Reverse Transcriptase Inhibitor

نویسندگان

  • Michael E. Pierce
  • Rodney L. Parsons
  • Lilian A. Radesca
  • Young S. Lo
  • Stuart Silverman
  • James R. Moore
  • Qamrul Islam
  • Anusuya Choudhury
  • Joseph M. D. Fortunak
  • Dieu Nguyen
  • Chi Luo
  • Susan J. Morgan
  • Wayne P. Davis
  • Pat N. Confalone
  • Cheng-yi Chen
  • Richard D. Tillyer
  • Lisa Frey
  • Lushi Tan
  • Feng Xu
  • Dalian Zhao
  • Andrew S. Thompson
  • Edward G. Corley
  • Edward J. J. Grabowski
  • Robert Reamer
  • Paul J. Reider
چکیده

A highly enantioselective and practical synthesis of the HIV-1 reverse transcriptase inhibitor efavirenz (1) is described. The synthesis proceeds in 62% overall yield in seven steps from 4-chloroaniline (6) to give efavirenz (1) in excellent chemical and optical purity. A novel, enantioselective addition of Li-cyclopropyl acetylide (4a) to p-methoxybenzyl-protected ketoaniline 3a mediated by (1R,2S)-N-pyrrolidinylnorephedrine lithium alkoxide (5a) establishes the stereogenic center in the target with a remarkable level of stereocontrol.

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تاریخ انتشار 1998