The present invention relates to 1-aza-bicy-cloalkyl derivatives of Formula (I); wherein the substituents are as defined in the specification, to processes for their production, their use as pharmaceuticals and to pharmaceutical compositions comprising them. Formula (I), wherein A represents O or N(R′); Y represents a group of formula, or wherein the left bond is attached to the A group and the right bond is attached to the R group; R represents a substituted or unsubstituted C
5
-C
10
aryl, substituted or unsubstituted hetero-C
5
-C
10
aryl, a group N(R
1
)(R
4
), or a group N(R
2
)(CHP
3
R
4
); R represent a hydrogen, C
1
-C
4
alkyl, or CF
3
; R
2
represents hydrogen, C
1
-C
4
alkyl, or CF
3
; R
3
represents hydrogen, C
1
-C
4
alkyl, or CF
3
; R
4
represents a substituted or unsubstituted C
5
-C
10
aryl or a substituted or unsubstituted C
5
-C
10
heteroaryl; in free base or acid addition salt form.
本发明涉及公式(I)的1-aza-bicy-cloalkyl衍
生物;其中取代基如规范中定义,以及它们的制备方法,它们作为药物的用途,以及包含它们的药物组成物。公式(I)中,A代表O或N(R′); Y代表公式的一个群体,或其中左键连接到A群体,右键连接到R群体;R代表取代或未取代的C5-C10芳基,取代或未取代的杂环C5-C10芳基,一个N(R1)(R4)群体或一个N(R2)(CHP3R4)群体;R代表氢,C1-C4烷基或
CF3;R2代表氢,C1-C4烷基或 ;R3代表氢,C1-C4烷基或 ;R4代表取代或未取代的C5-C10芳基或取代或未取代的C5-C10杂环芳基;以游离碱或酸加成盐形式存在。