Center for Integrative Chemical Biology and Drug Discovery, Division of Medicinal Chemistry and Natural Products, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, 27599, United States.
ACS Comb Sci. 2011 Jul 11;13(4):414-20. doi: 10.1021/co200039k. Epub 2011 May 10.
A concise and highly divergent synthetic route has been developed to rapidly access 1,3,6-trisubstituted pyrazolopyrimidines. The synthesis features a microwave assisted one-pot N1-alkylation/Suzuki-Miyaura reaction as the key step. The sequence of the synthetic scheme can be varied to selectively modify the N1, C3, or C6 position at a late synthetic stage, thereby providing a highly efficient approach to explore the structure-activity relationships of pyrazolopyrimidine derivatives. The scope of these reactions has also been explored.
现已开发出一种简洁且高度多样化的合成途径,可快速获得 1,3,6-三取代的吡唑并嘧啶。该合成的关键步骤是微波辅助一锅法 N1-烷基化/Suzuki-Miyaura 反应。合成方案的顺序可以变化,以在后期合成阶段选择性修饰 N1、C3 或 C6 位置,从而为探索吡唑并嘧啶衍生物的结构-活性关系提供了一种高效的方法。还探索了这些反应的范围。