Zhong Bin, Chen Feng, Ge Yushu, Liu Dan
Heifei National Laboratory for Physical Sciences at Microscale, the CAS Key Laboratory of Innate Immunity and Chronic Disease, School of Basic Medical Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230027, People's Republic of China.
The First Affiliated Hospital of University of Science and Technology of China, Hefei, Anhui 230001, People's Republic of China.
R Soc Open Sci. 2023 Oct 4;10(10):231263. doi: 10.1098/rsos.231263. eCollection 2023 Oct.
The carbon-nitrogen double bond (C=N) is a fundamentally important functional group in organic chemistry. This is largely due to the fact that C=N acts as electrophilic synthon to give nitrogen-containing compounds. Here, we report the condensation of primary amine or hydrazine with very electron-deficient aldehyde to form C=N bond in the absence of any catalysts (metals and acids). The protocol performs at room temperature and applies water as co-solvent. Two hundred examples are presented here. With its intrinsic advantages of wide substrate scopes, excellent efficiency (high yields and short reaction time), operational simplicity, mild condition (room temperature as reaction temperature, no catalysts, no additions, water as co-solvent and opening to air) and available starting materials, the protocol can be compatible with various drugs, prodrugs, dyes and pharmacophores containing primary amino group. In addition, we also successfully apply this protocol to rapidly synthesize the core scaffolds of bioactive molecules.
碳氮双键(C=N)是有机化学中一个至关重要的官能团。这主要是因为C=N作为亲电合成子可用于制备含氮化合物。在此,我们报道了在无任何催化剂(金属和酸)的情况下,伯胺或肼与电子极度缺乏的醛缩合形成C=N键。该方法在室温下进行,并使用水作为共溶剂。本文给出了200个实例。该方法具有底物范围广、效率高(高收率和短反应时间)、操作简单、条件温和(室温作为反应温度、无催化剂、无添加剂、水作为共溶剂且暴露于空气中)以及起始原料易得等固有优点,可与各种含有伯氨基的药物、前药、染料和药效基团兼容。此外,我们还成功地将该方法应用于快速合成生物活性分子的核心骨架。