Reactions and Reactivity of Thienopyridines: Facile Synthesis of Some Pyridothienooxazepine Derivatives
作者:Y. A. El-Osaily、A. A. O. Sarhan、A. M. Kamal El-Dean
DOI:10.1080/10426500600883122
日期:2007.1.1
Pyridothienooxazepines were synthesized by the interaction salt of the 3-aminothienopyridine-2-carboxylate with activated α-haloketones or α-halonitriles. Several derivatives of thienopyridine were prepared either by the replacement of an amino group or by using an amino group in 3-aminothienopyridine-2-carboxylate to synthesize another derivative of thienopyridine.
Pyridothienooxazepines 是通过 3-aminothienopyridine-2-carboxylate 与活化的 α-卤代酮或 α-卤腈的相互作用盐合成的。几种噻吩并吡啶衍生物是通过取代氨基或通过使用 3-氨基噻吩并吡啶-2-羧酸酯中的氨基合成另一种噻吩并吡啶衍生物来制备的。