产量(工程)
化学
尿素
激酶
癌症
药理学
组合化学
癌症研究
生物化学
医学
内科学
材料科学
冶金
作者
Donald Bankston,Jacques Dumas,Reina Natero,Bernd Riedl,Mary-Katherine Monahan,Robert Sibley
摘要
Urea 3 (BAY 43-9006), a potent Raf kinase inhibitor, was prepared in four steps with an overall yield of 63%. Significant process research enabled isolation of each intermediate and target without chromatographic purification, and overall yield increases >50% were observed compared to those from previous methods. This report focuses on improved synthetic strategies for production of scaled quantities of 3 for preclinical, toxicological studies. These improvements may be useful to assemble other urea targets as potential therapeutic agents to combat cancer.
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