申请人:——
公开号:US20030139421A1
公开(公告)日:2003-07-24
Compounds of general formula I
1
R
1
is selected from any one of pyridinyl, thienyl, furanyl,
imidazolyl, and triazolyl;
where each R
1
heteroaromatic ring may optionally and independently be further substituted by
1, 2
or
3
substituents selected from straight and branched C
1
-C
6
alkyl, NO
2
, CF
3
, C
1
-C
6
alkoxy, chloro, fluoro, bromo, and iodo. The substitutions on the heteroaromatic ring may take place in any position on said ring systems;
are disclosed and claimed in the present application, as well as separate enantiomers of the compounds and salts and pharmaceutical compositions comprising the novel compounds and their use in therapy, in particular in the management of pain.
通式I1R1的化合物被选择自吡啶基、噻吩基、呋喃基、咪唑基和三唑基中的任意一种;其中每个R1杂环芳香环可以选择性地且独立地进一步被1、2或3个来自直链和支链C1-C6烷基、NO2、CF3、C1-C6烷氧基、氯、氟、溴和碘的取代基所取代。杂环芳香环上的取代基可以发生在该环系统的任何位置;本申请公开和声称了所述化合物的单独对映体以及包含新化合物的盐和药物组成物,并且它们在治疗中的使用,特别是在疼痛管理中。