共 62 条
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.
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页码:2197 / 2200
页数:4
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