| 主权项 |
1. A method of producing a compound represented by formula (I): or a pharmacologically acceptable salt thereof, wherein Ar1 and Ar2 are each independently a heteroaryl group; R1, R2 and R3 are each independently a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group, a C3-C7 cycloalkyl group or a cyano group; R4 and R5 are each independently a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group, a C3-C7 cycloalkyl group or a C1-C6 alkoxy group; and n is an integer of 1 to 3; wherein the heteroaryl group is optionally substituted with one or two groups independently selected from a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group, a C3-C7 cycloalkyl group, a carboxy group, a cyano group, an amino group, a C1-C3 alkylamino group and a di-C1-C3 alkylamino group; and when the heteroaryl group is substituted with two such groups, the two groups are the same as or different from each other, comprising a step of removing a protecting group, P, from the compound of formula (VI) |
