化学
产量(工程)
试剂
甲酰胺
亚硝化
药物化学
有机化学
酰胺
组合化学
恶二唑
冶金
材料科学
作者
Shaoqing Du,Jin Li,Wen Fu,Xiaoyong Xu,Xusheng Shao,Xuhong Qian
标识
DOI:10.1016/j.tetlet.2021.153209
摘要
Abstract 1,2,4-Oxadiazole-3-carboxamide has been extensively used in the pharmaceutical chemistry. In this study, 1,2,4-oxadiazole-3-carboxamide is accomplished through an acid-promoted reaction of N-(cyanomethyl)amide with nitrosation reagent. This novel preparation of 1,2,4-oxadiazole-3-carboxamide was carried out at 25 °C, and the yield of target compounds was as high as 92%. At the same time, the amount of acid used is reduced. A mechanism speculation for the formation of 1,2,4-oxadiazole-3-carboxamide has been provided. The new synthetic method provides great convenience for the synthesis of compounds containing 1,2,4-oxadiazole-3-carboxamide.
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