Synthesis of a Library of N-monofluoromethyl Compounds from N-monofluoromethyl Carbamoyl/Thiocarbamoyl Fluorides.

Liye Ma, Lvqi Jiang, Guangsheng Tian, Zijian Lin, Zhongquan Lin, Yu Xu, Zihao Guo, Leibing Wang, Jie Liu, Wen-Bin Yi
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Abstract

The distinctive chemical properties of fluorine atoms have enabled fluorine-containing compounds to make significant strides in the pharmaceutical and materials fields. However, due to the very limited synthetic methods, the enormous potential of N-monofluoromethyl compounds has not yet been unlocked. In this study, we present an operationally simple and practical protocol for various largely underexplored N-monofluoromethyl compounds, utilizing two powerful and isolable building blocks: N-CH2F thio carbamoyl fluorides and N-CH2F carbamoyl fluorides. Additionally, the reactivity of fluorine atoms located at different positions of the two building blocks toward nucleophilic substitution was investigated both experimentally and theoretically.

n -单氟甲基氨基甲酰/硫氨基甲酰氟化物合成n -单氟甲基化合物库。
氟原子独特的化学性质使含氟化合物在医药和材料领域取得了重大进展。然而,由于合成方法非常有限,n -单氟甲基化合物的巨大潜力尚未得到释放。在这项研究中,我们提出了一种操作简单实用的方案,用于各种尚未开发的n -单氟甲基化合物,利用两种强大且可分离的构建块:N-CH2F硫代氨基甲酰氟化物和N-CH2F氨基甲酰氟化物。此外,在实验和理论上研究了位于两个构建单元不同位置的氟原子对亲核取代的反应性。
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