Heterocyclylamide-substituted thiazoles, pyrroles and thiophenes

A compound of the formula

• in which
• R1 represents a group of the formula
• where
• * represents the point of attachment to the carbonyl group,
• R3 represents phenyl or 5- or 6-membered heteroaryl,
• where phenyl and heteroaryl may be substituted by 1 to 3 substituents, where the substituents independently of one another are selected from the group consisting of halogen, hydroxyl, oxo, nitro, cyano, trifluoromethyl, difluoromethyl, trifluoromethoxy, difluoromethoxy, monofluoromethoxy, trifluoromethylthio, C1-C6-alkyl, C1-C6-alkoxy, hydroxycarbonyl, C1-C6-alkoxycarbonyl, amino, C1-C6-alkylamino, aminocarbonyl and C1-C6-alkylaminocarbonyl,
• R4 represents phenyl or 5- or 6-membered heteroaryl,
• where phenyl and heteroaryl may be substituted by 1 to 3 substituents, where the substituents independently of one another are selected from the group consisting of halogen, hydroxyl, oxo, nitro, cyano, trifluoromethyl, difluoromethyl, trifluoromethoxy, difluoromethoxy, monofluoromethoxy, trifluoromethylthio, C1-C6-alkyl, C1-C6-alkoxy, hydroxycarbonyl, C1-C6-alkoxycarbonyl, amino, C1-C6-alkylamino, aminocarbonyl and C1-C6-alkylaminocarbonyl,
• and
• R5 and R6 independently of one another represent hydrogen, methyl or ethyl,
• R2 represents phenyl,
• where phenyl may be substituted by 1 to 3 substituents, where the substituents independently of one another are selected from the group consisting of halogen, hydroxyl, trifluoromethyl, difluoromethyl, trifluoromethoxy, difluoromethoxy, monofluoromethoxy, trifluoromethylthio, C1-C6-alkyl and C1-C6-alkoxy,
• A represents a group of the formula
• where
• * represents the point of attachment to the carbonyl group,
• # represents the point of attachment to the nitrogen atom of the urea,
• R7 represents C1-C6-alkyl,
• where alkyl may be substituted by one substituent, where the substituent is selected from the group consisting of C3-C6-cycloalkyl, C6-C10-aryl and 5- or 6-membered heteroaryl,
• where cycloalkyl, aryl and heteroaryl may be substituted by 1 to 3 substituents, where the substituents independently of one another are selected from the group consisting of halogen, hydroxyl, oxo, nitro, cyano, trifluoromethyl, difluoromethyl, trifluoromethoxy, difluoromethoxy, monofluoromethoxy, trifluoromethylthio, C1-C6-alkyl, C1-C6-alkoxy, hydroxycarbonyl, C1-C6-alkoxycarbonyl, amino, C1-C6-alkylamino, aminocarbonyl and C1-C6-alkylaminocarbonyl,
• and
• R8 and R9 represent, independently of one another, hydrogen, halogen or C1-C6-alkyl,
• where alkyl may be substituted by one substituent, where the substituent is selected from the group consisting of C3-C6-cycloalkyl, C6-C1o-aryl and 5- or 6-membered heteroaryl,
• in which cycloalkyl, aryl and heteroaryl may be substituted by 1 to 3 substituents, where the substituents independently of one another are selected from the group consisting of halogen, hydroxyl, oxo, nitro, cyano, trifluoromethyl, difluoromethyl, trifluoromethoxy, difluoromethoxy, monofluoromethoxy, trifluoromethylthio, C1-C6-alkyl, C1-C6-alkoxy, hydroxycarbonyl, C1-C6-alkoxycarbonyl, amino, C1-C6-alkylamino, aminocarbonyl and C1-C6-alkylaminocarbonyl,
• or a salt thereof.