摘要 |
The present invention provides a novel method for producing a compound represented by general formula (VII), a pharmaceutically acceptable salt thereof or a synthesis intermediate thereof. (In the formula, R2 represents a hydrogen atom or a halogen atom; RC represents a C1-6 alkyl group; X represents a group that is selected from among heteroaryl groups and the like; R11 represents an atom or group that is selected from among a hydrogen atom, a halogen atom, a C1-6 alkyl group and the like; each of R16 and R17 independently represents an atom or group that is selected from among a hydrogen atom, a C1-6 alkyl group and the like; and R15 represents a hydrogen atom or a C1-6 alkyl group.) |