3,4-二取代-3-(二氟甲基)吡唑类化合物的构建  

Construction of 3,4-Disubstituted-3-(difluoromethyl)pyrazoles

作　　者：曾俊良 许志红[1] 马军安[2] Zeng Junliang;Xu Zhihong;Ma Junan(School of Chemistry and Chemical Engineering,Xuchang University,Henan 461000;Tianjin Key Laboratory of Molecular Optoelectronic Sciences,and Tianjin Collaborative Innovation Center of Chemical Science&Engineering,Department of Chemistry,Tianjin University,Tianjin 300072)

机构地区：[1]许昌学院化学化工学院,许昌461000 [2]天津大学化学系天津市分子光电科学重点实验室天津化学化工协同创新中心,天津300072

出　　处：《有机化学》2020年第5期1105-1116,共12页Chinese Journal of Organic Chemistry

基　　金：河南省高等学校重点科研(No.20A150039)资助项目。

摘　　要：二氟甲基在活性分子中可以起到氢键供体、生物电子等排体、亲脂性调节等作用,在药物和农药分子的设计中被广泛使用.3,4-二取代-3-(二氟甲基)吡唑骨架的发现及应用是该领域的一个突出代表,研究表明含有这类骨架的分子能够抑制琥珀酸脱氢酶(SDHIs),具有作为杀菌剂的潜力,目前市场上已有近十种农药分子含有3,4-二取代-3-(二氟甲基)吡唑结构单元,年销售额高达十几亿美元.按照所用含氟砌块的不同种类,对近二十年来3,4-二取代-3-(二氟甲基)吡唑类化合物的合成方法进行总结和展望.The CHF2 moiety has been widely utilized in the design of pharmaceuticals and agrochemicals,because this group can act as hydrogen-bonding donor to improve the binding selectivity of biologically active compounds,as a bioisostere to substitute for methyl,methoxy,hydroxy,amino and thiol groups,and as a lipophilic regulator to improve the liposolubility of the active compounds.For example,3-difluoromethylpyrazole scaffolds are present in many organic compounds that exhibit important biological activities.In this content,there are nearly ten kinds of pesticide molecules on the market that contain 3,4-disubstituted-3-(difluoromethyl)pyrazole units,with annual sales of up to one billion dollars.In this review,the methods of construction of 3,4-disubstituted 3-difluoromethylpyrazoles will been briefly summarized that have been reported so far.Four different strategies including using fluorinated reagents as substrates,difluoroacetic acid and its derivatives as fluorine building blocks,difluorodiazonium and others as fluorine building blocks will be introduced.

关 键 词：3 4-二取代-3-(二氟甲基)吡唑 二氟甲基杂环化合物 杀菌剂 合成 

分 类 号：O626[理学—有机化学]