Shang Zhenhua, Jiao Dechen, Cheng Haoran, Huang Daowei
School of Chemical and Pharmaceutical Engineering, Hebei University of Science and Technology, Shijiazhuang 050018, China.
Hebei Research Center of Pharmaceutical and Chemical Engineering, Shijiazhuang 050018, China.
Molecules. 2024 Dec 22;29(24):6048. doi: 10.3390/molecules29246048.
The 2-(4-hydroxyphenoxy)benzamide scaffold is frequently found in a variety of bioactive compounds, displaying a broad spectrum of properties, such as antibacterial and antitumor effects. In this study, we developed a new method for synthesizing 2-(4-hydroxyphenoxy)benzamide derivatives from 2-aryloxybenzamide via a PhIO-mediated oxidation reaction. The optimal reaction conditions were established as follows: TFA was used as the solvent, PhIO served as the oxidant with a substrate-to-oxidant ratio of 1:2, and the reaction was conducted at room temperature. This method, characterized by mild reaction conditions, broad applicability, and a metal-free nature, considerably improves the accessibility of 2-(4-hydroxyphenoxy)benzamide derivatives, which have been challenging to prepare using previously reported methods.
2-(4-羟基苯氧基)苯甲酰胺骨架常见于多种生物活性化合物中,具有广泛的性质,如抗菌和抗肿瘤作用。在本研究中,我们开发了一种通过PhIO介导的氧化反应从2-芳氧基苯甲酰胺合成2-(4-羟基苯氧基)苯甲酰胺衍生物的新方法。确定的最佳反应条件如下:使用三氟乙酸作为溶剂,PhIO作为氧化剂,底物与氧化剂的比例为1:2,反应在室温下进行。该方法具有反应条件温和、适用性广和无金属的特点,大大提高了2-(4-羟基苯氧基)苯甲酰胺衍生物的可及性,而使用先前报道的方法制备这些衍生物具有挑战性。