Paraschiv Andrei, Maruzzo Valentina, Pettazzi Filippo, Magliocco Stefano, Inaudi Paolo, Brambilla Daria, Berlier Gloria, Cravotto Giancarlo, Martina Katia
Department of Drug Science and Technology, University of Turin, Via Pietro Giuria 9, 10125 Turin, Italy.
Present address: R&D Department, Farmabios S.P.A., Via Pavia 1, Gropello Cairoli, Italy.
Beilstein J Org Chem. 2025 Jul 15;21:1462-1476. doi: 10.3762/bjoc.21.108. eCollection 2025.
The C2-amination of benzoxazole offers wide-ranging potential for substrate expansion and the functionalisation of bioactive compounds. This study presents a green and efficient C-H amination, catalysed by CuCl and CuCl, in acetonitrile without acidic, basic or oxidant additives that is accelerated by microwave (MW) irradiation and is completed in 1.5-2 h. A solid Cu(I) catalyst supported on aminated silica made the process cost-effective and heterogeneous, thus simplifying work-up and minimising free copper in solution. The catalyst was found to be regeneratable and reusable for up to eight cycles. The optimised method facilitated the synthesis of various benzoxazole derivatives, demonstrating its versatility and practical applicability.
苯并恶唑的C2胺化反应为底物扩展和生物活性化合物的功能化提供了广泛的潜力。本研究展示了一种绿色高效的C-H胺化反应,该反应由CuCl和CuCl2催化,在乙腈中进行,无需添加酸性、碱性或氧化剂添加剂,通过微波(MW)辐射加速,1.5 - 2小时内即可完成。负载在胺化硅胶上的固体Cu(I)催化剂使该过程具有成本效益且为多相反应,从而简化了后处理并减少了溶液中的游离铜。该催化剂可重复再生使用多达八次。优化后的方法促进了各种苯并恶唑衍生物的合成,证明了其通用性和实际适用性。