N-Picolinamides as ligands for Ullmann-type C-N coupling reactions

被引:17
作者
Damkaci, Fehmi [1 ]
Alawaed, Abdulkhaliq [1 ]
Vik, Erik [1 ]
机构
[1] SUNY Coll Oswego, Dept Chem, Oswego, NY 13126 USA
关键词
Ullmann-type coupling; C-N bond formation; Heterocoupling; Copper catalyzed; N-Picolinamides; COPPER-CATALYZED AMINATION; ARYL HALIDES; BOND FORMATION; EFFICIENT CATALYST; CROSS-COUPLINGS; AMINO-ACID; ARYLATION; HETEROCYCLES; IMIDAZOLES; INDOLES;
D O I
10.1016/j.tetlet.2016.04.017
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The use of N-phenyl-2-pyridincarboxamide-1-oxide as a ligand with Cu2O in Ullmann type C-N bond formations between aryl halides and N-heteroaryls in common solvents, such as MeCN, DMF, and DMSO at 82-120 degrees C has been successfully demonstrated. The ligand is effective when only 4% equiv is used relative to the substrate. The reaction provided the corresponding products in coupling of electron-rich, electron poor, and ortho-substituted aryl halides, including ortho aryl-chlorides, in good to very good yields. N-arylation is selectively preferred at the benzyl position when ortho-halide benzyl bromide is reacted with one equivalent of pyrazole. However, di-N-arylation is achieved in very high yields when 2.5 equiv of pyrazole is used, providing a stoichiometric control over the coupling reaction. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2197 / 2200
页数:4
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