A present invention provides aromatic amide derivatives which have an agonism of V2 receptor, are useful as agents for the treatment or prevention of diabetes insipidus, nocturia, nocturnal enuresis, overactive bladder or the like, and are represented by the general formula (I):
wherein R
1
represents a hydrogen atom or a C
1-6
alkyl group which may have a substituent, R
2
is a hydrogen atom or a C
1-6
alkyl group, R
3
is a hydrogen atom, a C
1-6
alkyl group or the like, R
4
, R
5
and R
6
are independently a hydrogen atom, a halogen atom or the like, R
7
is a hydrogen atom, a heteroaryl group which may have a substituent, a C
3-8
cycloalkyl group, an amino group which may have a substituent or a C
1-6
alkoxy group which may have a substituted group;
M
1
is a single bond, a C
1-4
alkylene group or the like
Y is N or CR
F
(in the formula, R
F
represents a hydrogen atom, a C
1-6
alkyl group or the like
or a pharmaceutically acceptable salt thereof, or a prodrug thereof, or pharmaceutical compositions comprising the same and pharmaceutical uses thereof.
本发明提供了具有V2受体激动作用的芳香酰胺衍
生物,可用作治疗或预防尿崩症、夜尿症、夜间遗尿、过度活动膀胱等药物,其通式表示为(I):其中R1表示氢原子或C1-6烷基,可以有取代基,R2表示氢原子或C1-6烷基,R3表示氢原子、C1-6烷基或类似物,R4、R5和R6分别表示氢原子、卤原子或类似物,R7表示氢原子、可以有取代基的杂环芳基、C3-8环烷基、可以有取代基的
氨基或C1-6烷氧基;M1表示单键、C1-4烷基等,Y表示N或CRF(在公式中,RF表示氢原子、C1-6烷基或类似物的药物可接受的盐,或其前药,或包含它的制药组合物和制药用途)。