Synthesis of alkyl- and aryl-amino-substituted anthraquinone derivatives by microwave-assisted copper(0)-catalyzed Ullmann coupling reactions

被引:53
作者
Baqi, Younis [1 ]
Mueller, Christa E. [1 ]
机构
[1] Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, PSB, Bonn, Germany
关键词
SELECTIVE P2Y-RECEPTOR ANTAGONISTS; P2; RECEPTORS; BLUE; ANILINOANTHRAQUINONE DERIVATIVES; P2-RECEPTOR ANTAGONISTS; PHEOCHROMOCYTOMA CELLS; LIGANDS; IDENTIFICATION; IRRADIATION; INHIBITORS;
D O I
10.1038/nprot.2010.63
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This protocol describes the efficient, generally applicable Ullmann coupling reaction of bromaminic acid with alkyl-or aryl-amines in phosphate buffer under microwave irradiation using elemental copper as a catalyst. The reaction leads to a number of biologically active compounds. As a prototypical example, the synthesis of a new, potent antagonist of human platelet P2Y(12) receptors, which has potential as an antithrombotic drug, is described in detail. The optimized protocol includes a description of an appropriate reaction setup, thin layer chromatography for monitoring the reaction and a procedure for the isolation, purification and characterization of the anticipated product. The reaction is performed without the use of a glove box and there is no requirement for an inert atmosphere. The reaction typically proceeds within 2-30 min, the protocol, including workup, generally takes 1-3 h to complete.
引用
收藏
页码:945 / 953
页数:9
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