烷基
化学
芳基
废止
1,2,3-三唑
三唑
组合化学
分子
药物化学
有机化学
催化作用
作者
Hao‐Nan Liu,Hao‐Qiang Cao,Chi Wai Cheung,Jun‐An Ma
出处
期刊:Organic Letters
[American Chemical Society]
日期:2020-02-04
卷期号:22 (4): 1396-1401
被引量:28
标识
DOI:10.1021/acs.orglett.0c00006
摘要
Alkyl N-aryl 1,2,3-triazole-carboxylates are important molecules or intermediates in medicinal chemistry, but the synthesis of N2-aryl counterparts remains elusive. Herein, we describe a Cu-mediated annulation reaction of alkyl 3-aminoacrylates with aryldiazonium salts, both of which are readily available substrates. Furthermore, alkyl 2-aminoacrylates are also viable substrates. Diverse alkyl N2-aryl 1,2,3-triazole-carboxylates and their analogues can be rapidly prepared under mild conditions. Especially, this protocol allows one to access several druglike variants of carbonic anhydrase inhibitors and celecoxib.
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