Deirdre M. B. Hickey,Paul D. Leeson,Steven D. Carter,Michael Goodyear,Sarah Jones,Norman Lewis,Ian T. Morgan,Maria Mullane,Jane Y. Tricker
出处
期刊:Journal of the Chemical Society日期:1988-01-01卷期号: (12): 3097-3102被引量:12
标识
DOI:10.1039/p19880003097
摘要
A synthesis of L-3,5-dibromo-3′-[(6-oxo-l,6-dihydropyridazin-3-yl)methyl]thyronine-SK&F L-94901 (1), a novel, selective and potent thyromimetic – is described. The key step in this synthesis involves the formation of a hindered diaryl ether moiety. This paper describes an approach via oxidative coupling of the hindered phenols (2) and (3). Some by-products and impurities generated during the synthesis are discussed briefly.