CuI-catalyzed coupling reaction of β-amino acids or esters with aryl halides at temperature lower than that employed in the normal Ullmann reaction.: Facile synthesis of SB-214857

被引:243
作者
Ma, DW [1 ]
Xia, CF [1 ]
机构
[1] Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R China
关键词
D O I
10.1021/ol016258r
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[GRAPHICS] The Cul-catalyzed coupling reaction of aryl halides with beta -amino acids or beta -amino esters is completed at 100 degreesC in 48 h, which indicates that the structure of the,beta -amino acid has an accelerating effect for the Ullmann-type aryl amination reaction. This coupling reaction can be used to prepare enantiopure N-aryl beta -amino acids. An efficient synthetic route to SB214857, a potent GPIIb/IIIa receptor antagonist, is developed using this method.
引用
收藏
页码:2583 / 2586
页数:4
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