当前位置: X-MOL 学术Heterocycl. Commun. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Synthesis of 1,2,3 triazole-linked benzimidazole through a copper-catalyzed click reaction
Heterocyclic Communications ( IF 2.3 ) Pub Date : 2019-11-28 , DOI: 10.1515/hc-2019-0016
Mohammad Bakherad 1 , Ali Keivanloo 1 , Amir H. Amin 1 , Amir Farkhondeh 1
Affiliation  

Abstract An efficient method has been developed for the synthesis of 1,2,3 triazole-linked benzimidazole through a copper-catalyzed click reaction in ethanol at 50°C. A broad range of aromatic azides were successfully reacted with n-propynylated benzimidazole via copper-catalyzed azide-alkyne cycloaddition reactions in the absence of a ligand. This method offers many advantages including short reaction times, low cost, and simple purification procedures.

中文翻译:

通过铜催化点击反应合成 1,2,3 三唑连接的苯并咪唑

摘要 开发了一种通过铜催化点击反应在 50°C 乙醇中合成 1,2,3 三唑连接的苯并咪唑的有效方法。在没有配体的情况下,通过铜催化的叠氮化物-炔环加成反应,多种芳香族叠氮化物与正丙炔化苯并咪唑成功反应。该方法具有许多优点,包括反应时间短、成本低和纯化程序简单。
更新日期:2019-11-28
down
wechat
bug