This invention provides quinazoline analogs of Formula I:
where A is bonded to at least one of the carbons at the 5, 6, 7 or 8 position of the bicyclic ring, and the ring is substituted by up to two independent R
3
groups. The invention also includes methods of using compounds of Formula I as type I receptor tyrosine kinase inhibitors and for the treatment of hyperproliferative diseases such as cancer.
                            本发明提供了公式I的
喹唑啉类似物:其中A与双环环上的5、6、7或8位置中的至少一个碳键结合,并且该环被高达两个独立的R3基团取代。本发明还包括使用公式I化合物作为I型受体
酪氨酸激酶
抑制剂和治疗癌症等增生性疾病的方法。