FIELD: medicine, pharmaceutics.
SUBSTANCE: present invention refers to new benzothiazolone derivatives of formula (I) or to their pharmaceutically acceptable salts showing β2-adrenoreceptor agonist activity, to a method for producing and using them for preparing a drug. wherein Ra and Rb independently represent hydrogen; R1 represents: α- or β-branched C3-12alkyl (optionally substituted by hydroxy, OC(O)(C1-6alkyl)), CH2(C3-12cycloalkyl) wherein cycloalkyl is optionally condensed with a benzene ring, C3-12cycloalkyl (optionally substituted by halogen, C1-6alkyl) or R28; R6 represents a phenyl or 5- or 6-phenyl heteroaromatic ring (each of which is optionally substituted by halogen, trifluoromethyl, hydroxy, C1-6alkyl, -C(O)NHR13, -SO2NHR14, C1-6alkoxy, optionally substituted by halogen), C1-6halogenoalkyl, benzodioxolyl, benzothiazolyl substituted by oxo and hydroxy group; R2, R3 and R4 independently represent hydrogen or C1-6alkyl; R29 represents hydrogen; R4 represents hydrogen, hydroxy or C1-6alkyl. The values R13, R14 and R28 are those as specified in the patent claim.
EFFECT: producing the pharmaceutically acceptable salts showing β2-adrenoreceptor agonist activity.
10 cl, 1 tbl, 105 ex
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Authors
Dates
2012-07-10—Published
2007-12-19—Filed