作者:Yu. N. Klimochkin、E. A. Ivleva
DOI:10.1134/s1070428022050050
日期:2022.5
Abstract N-Adamantylated amides have been synthesized from 1-adamantyl nitrate. The reactions were carried out in the sulfuric acid media. The proposed method is usefulness for the preparation of antiviral drug tromantadine. A number of new cage aminoamides have been synthesized by reactions of N-(1-adamantyl)-2-chloroacetamide with nitrogen-containing nucleophiles. with potential biological activity
摘要 N-金刚烷基化的酰胺是由 1-金刚烷基硝酸盐合成的。反应在硫酸介质中进行。所提出的方法可用于制备抗病毒药物曲金刚乙胺。N -(1-金刚烷基)-2-氯乙酰胺与含氮亲核试剂反应合成了许多新的笼形氨基酰胺。具有潜在的生物活性。