This invention provides a class of 3-amino-7H-thieno[2,3-b]pyridin-6-one derivatives, substituted in the 7-position by an aryl, heteroaryl, cycloalkyl or heterocycloalkyl moiety, and in the 2-position by a specified range of substituent groups; also provided is a process for preparing those compounds, and the use thereof as intermediates in the manufacture of certain p38 MAP kinase inhibitors.
本发明提供了一类在7位被芳基、杂芳基、环烷基或杂环烷基基团取代,在2位被特定范围的取代基团取代的3-
氨基-7H-
噻吩[2,3-b]
吡啶-6-酮衍
生物;还提供了制备这些化合物的方法,以及它们作为某些p38
MAP激酶
抑制剂中间体的用途。