A convergent, scalable synthesis of HIV protease inhibitor PNU-140690

被引:35
作者
Fors, KS [1 ]
Gage, JR [1 ]
Heier, RF [1 ]
Kelly, RC [1 ]
Perrault, WR [1 ]
Wicnienski, N [1 ]
机构
[1] Pharmacia & Upjohn Inc, Chem proc Res & Preparat, Kalamazoo, MI 49001 USA
关键词
D O I
10.1021/jo9809229
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
PNU-140690, an inhibitor of the HIV protease enzyme undergoing clinical evalution as a chemotherapeutic agent for treatment of AIDS, was synthesized by a convergent approach amenable to large-scale preparation in a pilot plant environment. The key step is the aldol addition of nitroaromatic ester (+)-8 to aldehyde 19e. The two stereocenters present in the target molecule were each set independently by resolution of enantiomers. Intermediates along the synthetic routes were chosen to maximize opportunities for isolation and purification by crystallization.
引用
收藏
页码:7348 / 7356
页数:9
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