Ruthenium-Catalyzed Regioselective C7–H Arylation of 2-(Het)aryl[1,2,4]triazolo[1,5-a]pyrimidines with Aryl Halides

IF 0.8 4区 化学 Q4 CHEMISTRY, ORGANIC Russian Journal of Organic Chemistry Pub Date : 2024-08-30 DOI:10.1134/s1070428024060095
K. E. Shepelenko, I. G. Gnatiuk, V. M. Chernyshev
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Abstract

Unusual direction of the C–H arylation of 2-(het)aryl[1,2,4]triazolo[1,5-a]pyrimidines with (het)aryl halides under catalysis by ruthenium(II) complexes has been revealed. The reaction involved activation of the C7–H bond rather than the Cα–H bond of the (het)aryl substituent at C2 of the triazolopyrimidine core. The arylation of 2-substituted [1,2,4]triazolo[1,5-a]pyrimidines with (het)aryl bromides afforded a series of 7-(het)aryl derivatives in good yields.

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钌催化的 2-(Het)芳基[1,2,4]三唑并[1,5-a]嘧啶与芳基卤化物的区域选择性 C7-H 芳基化反应
摘要 在钌(II)配合物的催化下,2-(het)芳基[1,2,4]三唑并[1,5-a]嘧啶与(het)芳基卤化物的 C-H 芳基化方向被揭示出来。该反应涉及活化三唑并嘧啶核心 C2 处(het)芳基取代基的 C7-H 键而不是 Cα-H 键。将 2-取代的 [1,2,4]三唑并[1,5-a]嘧啶与 (庚)芳基溴化物进行芳基化反应,得到了一系列 7-(庚)芳基衍生物,产率良好。
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来源期刊
CiteScore
1.40
自引率
25.00%
发文量
139
审稿时长
3-6 weeks
期刊介绍: Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.
期刊最新文献
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