Department of Organic Chemistry, Faculty of Science, Palacký University, 17. listopadu 12, 771 46 Olomouc, Czech Republic.
Molecules. 2021 Mar 14;26(6):1603. doi: 10.3390/molecules26061603.
In this report, we employed the solid-phase synthetic approach to prepare variously substituted dihydropteridinones, tetrahydropyrrolopteridinones, and pyrimidodiazepinones, using a versatile building block-4,6-dichloro-5-nitropyrimidine. All these compounds are pharmacologically significant scaffolds of the great importance of medicinal chemists. The fast and efficient synthetic methodology is highly desirable for defining their structure-activity relationship (SAR) and optimizing pharmacokinetic properties. Our research efforts utilize simple synthetic methods to generate a library of analogues for future SAR studies. The efficiency of our approach was exemplified in various pteridinones as well as pyrimidodiazepinones.
在本报告中,我们采用固相合成方法,使用多功能砌块-4,6-二氯-5-硝基嘧啶,制备了各种取代的二氢喋啶酮、四氢吡咯并[2,3-d]嘧啶酮和嘧啶并[1,2-a]二氮杂卓酮。所有这些化合物都是药物化学家非常重要的药理学上有意义的支架。快速高效的合成方法对于确定它们的结构-活性关系(SAR)和优化药代动力学性质非常重要。我们的研究工作利用简单的合成方法生成了一个类似物库,用于未来的 SAR 研究。我们的方法的效率在各种喋啶酮和嘧啶并[1,2-a]二氮杂卓酮中得到了例证。