Yang Yanmei, Liu Junmin, Chen Zhenzhen, Niu Weihua, Li Ran, Niu Le, Yang Peng, Mu Xiaoyan, Tang Bo
Key Laboratory of Molecular and Nano Probes, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Ministry of Education, Jinan, China.
Front Chem. 2020 Sep 10;8:789. doi: 10.3389/fchem.2020.00789. eCollection 2020.
Quinoxaline derivatives demonstrate many distinguished chemical, biological, and physical properties and have a wide application in dyes, electroluminescent material, organic semiconductors, biological agents, etc. However, the synthesis of quinoxaline still suffers from several drawbacks, for instance, longer reaction time, unsatisfactory yields, and use of metal catalysts. Here, utilizing microdroplet-assisted reaction, we demonstrate the successive synthesis of several important quinoxaline derivatives. For case studies of 1H-indeno [1, 2-b] quinoxaline and 3,5-dimethyl-2-phenylquinoxaline, the present microdroplet approach can complete in milliseconds and the conversion rate reached 90% without adding any catalyst, which is considerably quicker and higher than conversional bulk-phase reactions. When combined with MS detection, high-throughput screening of the optimal reaction conditions can be achieved. Several impacts of droplet volume, reaction flow rate, distance from the MS inlet, spray voltage, and flow rate of the auxiliary gas can be screened on-site quickly for enhanced reaction speed and yields. More importantly, this platform is capable to be used for the scaled-up microdroplet synthesis of quinoxaline diversities. Considering the facile, economic, and environmentally friendly features of the microdroplet approach, we sincerely hope that the current strategy can effectively promote the academic research and industrial fabrications of functional quinoxaline substances for chemical, biological, and pharmaceutical application developments.
喹喔啉衍生物具有许多独特的化学、生物学和物理性质,在染料、电致发光材料、有机半导体、生物制剂等方面有广泛应用。然而,喹喔啉的合成仍存在一些缺点,例如反应时间长、产率不理想以及使用金属催化剂。在此,我们利用微滴辅助反应展示了几种重要喹喔啉衍生物的连续合成。以1H-茚并[1,2-b]喹喔啉和3,5-二甲基-2-苯基喹喔啉为例,当前的微滴方法在不添加任何催化剂的情况下可在毫秒内完成,转化率达到90%,这比传统的本体相反应快得多且转化率更高。当与质谱检测相结合时,可实现最佳反应条件的高通量筛选。可以快速现场筛选微滴体积、反应流速、距质谱入口的距离、喷雾电压和辅助气体流速等因素的多种影响,以提高反应速度和产率。更重要的是,该平台能够用于喹喔啉多样性的放大微滴合成。考虑到微滴方法简便、经济且环保的特点,我们真诚希望当前策略能够有效促进用于化学、生物学和药物应用开发的功能性喹喔啉物质的学术研究和工业制造。