Gautam Nimisha, Logdi Ratan, P Sreejyothi, Roy Antara, Tiwari Ashwani K, Mandal Swadhin K
Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur Campus Nadia 741246 West Bengal India
Department of Chemistry, Indian Institute of Technology Kharagpur Kharagpur 721302 West Bengal India.
Chem Sci. 2023 Apr 20;14(19):5079-5086. doi: 10.1039/d3sc01216f. eCollection 2023 May 17.
Herein, we report the first catalytic methylation of primary amides using CO as a C1 source. A bicyclic (alkyl)(amino)carbene (BICAAC) exhibits dual role by activating both primary amide and CO to carry out this catalytic transformation which enables the formation of a new C-N bond in the presence of pinacolborane. This protocol was applicable to a wide range of substrate scopes, including aromatic, heteroaromatic, and aliphatic amides. We successfully used this procedure in the diversification of drug and bioactive molecules. Moreover, this method was explored for isotope labelling using CO for a few biologically important molecules. A detailed study of the mechanism was carried out with the help of spectroscopic studies and DFT calculations.
在此,我们报道了首例使用CO作为C1源对伯酰胺进行催化甲基化反应。一种双环(烷基)(氨基)卡宾(BICAAC)通过同时活化伯酰胺和CO发挥双重作用,从而实现这种催化转化,该转化能够在频哪醇硼烷存在下形成新的C-N键。该方案适用于广泛的底物范围,包括芳香族、杂芳香族和脂肪族酰胺。我们成功地将该方法用于药物和生物活性分子的多样化合成。此外,还探索了该方法用于一些具有生物学重要性的分子的CO同位素标记。借助光谱研究和密度泛函理论(DFT)计算对反应机理进行了详细研究。