The substituted groups of 2-aminopyrimidine derivatives were mainly alkyl, alkoxyl or halogen, while trifluoromethy-containing heterocyclic compounds were seldom reported. The synthesis routes were often heterocyclization first, and fluorization was followed.
现有嘧啶类衍生物的取代基团大都为烷基、烷氧基和卤素原子,含有三氟甲基的嘧啶类衍生物的报道比较少,且合成方法多为先合成杂环再经过氟化的方法。
参考来源 - 三氟甲基嘧啶衍生物及其磺酰脲类化合物的合成研究·2,447,543篇论文数据,部分数据来源于NoteExpress
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