Department of Chemistry, Purdue University, Bindley Bioscience Center, 1203 West State Street, West Lafayette, Indiana 47907, United States.
Davidson School of Chemical Engineering, Purdue University, West Lafayette, Indiana 47907-2100, United States.
ACS Comb Sci. 2020 Apr 13;22(4):184-196. doi: 10.1021/acscombsci.9b00212. Epub 2020 Mar 16.
Nucleophilic aromatic substitution (SAr) reactions were optimized using high-throughput experimentation techniques for execution under flow conditions. A total of 3072 unique reactions were evaluated with an analysis time of ∼3.5 s per reaction using a system that combines a liquid handling robot for reaction mixture preparation with desorption electrospray ionization (DESI) mass spectrometry (MS) for analysis. The reactions were performed in bulk microtiter arrays with and without incubation. In-house developed software was used to process the data and generate heat maps of the results. This information was then used to select the most promising conditions for continuous synthesis under microfluidic reactor conditions. Our results show that this HTE approach provides robust guidance for narrowing the range of conditions needed for optimization of SAr reactions.
亲核芳香取代(SAr)反应采用高通量实验技术进行优化,以便在流动条件下进行。使用一种将用于反应混合物制备的液体处理机器人与解吸电喷雾电离(DESI)质谱(MS)分析相结合的系统,对总共 3072 个独特的反应进行了评估,每个反应的分析时间约为 3.5 秒。反应在带有和不带有孵育的批量微滴定板阵列中进行。使用内部开发的软件来处理数据并生成结果的热图。然后,使用此信息选择最有前途的条件,以便在微流控反应器条件下进行连续合成。我们的结果表明,这种 HTE 方法为缩小 SAr 反应优化所需的条件范围提供了可靠的指导。