Synthesis of selectively trifluoromethylated pyridine derivaties as potential antihypertensives
作者:Robert W. Lang、Paul F. Wenk
DOI:10.1002/hlca.19880710312
日期:1988.5.4
A general synthesis of selectively 6-(trifluoromethyl)-substitued 2(1H)-pyridinones is described. Further transformation of one of these compounds leads to the new CF3-containing potassium-channel openers 2a and 2b.
描述了选择性6-(三氟甲基)取代的2(1H)-吡啶酮的一般合成。这些化合物之一的进一步转化导致新的含CF 3的钾通道开放剂2a和2b。