Institut Curie, Centre de Recherche, 26 rue d'Ulm, Paris F-75248, France.
J Org Chem. 2012 Jun 1;77(11):5006-16. doi: 10.1021/jo300481s. Epub 2012 May 18.
A general and efficient procedure for the synthesis of 2,3-disubstituted 5-azaindoles through the palladium-catalyzed heteroannulation of 4-acetamido-3-iodopyridines and diaryl-, dialkyl-, or arylalkylalkynes is described along with a study of the reaction regioselectivity. The preparation of 2-monosubstituted 5-azaindoles via sila-Sonogashira/5-endo cyclization is also reported. These methods allowed us to prepare 36 diversely substituted 5-azaindoles in good yields.
通过钯催化的 4-乙酰氨基-3-碘吡啶与二芳基、二烷基或芳基烷基炔的杂环化反应,描述了一种通用且高效的合成 2,3-二取代 5-氮杂吲哚的方法,并对反应的区域选择性进行了研究。还报道了通过硅基-Sonogashira/5-endo 环化反应制备 2-单取代 5-氮杂吲哚的方法。这些方法使我们能够以良好的收率制备 36 种不同取代的 5-氮杂吲哚。