The present invention relates to bicyclic heterocycles of general formula
wherein
R
a
, R
b
, R
c
, R
d
, X and n are defined as in claim 1, the tautomers, the stereoisomers, the mixtures thereof and the salts thereof, particularly the physiologically acceptable salts thereof with inorganic or organic acids which have valuable pharmacological properties, particularly an inhibiting effect on the signal transduction mediated by tyrosine kinases, their use in treating diseases, particularly tumoral diseases, as well as benign prostatic hyperplasia (BPH), diseases of the lungs and respiratory tract and the preparation thereof.
本发明涉及一般式为的双环
杂环化合物,其中Ra、Rb、Rc、Rd、X和n如权利要求1所定义,它们的互变异构体、立体异构体、混合物及其盐,特别是它们与无机或有机酸形成的生理上可接受的盐具有有价值的药理学特性,特别是对由
酪氨酸激酶介导的信号传导具有抑制作用,它们的用途在于治疗疾病,特别是肿瘤性疾病、良性前列腺增生症(BPH)、肺和呼吸道疾病以及其制备方法。