The present invention relates to compounds of general formula I wherein R1 is selected from a group consisting of -CH2-Ra, wherein Ra denotes C1-6-alkyl optionally mono- or polysubstituted with fluorine, or C3-6- cycloalkyl optionally mono- or polysubstituted with fluorine and optionally substituted with a group selected from among CH3, CF3, and CHF2, and Lp, (Het)Ar1, (Het)Ar2 and n are as defined in the application, which have valuable pharmacological properties, and in particular bind to the GPR119 receptor and modulate its activity.
本发明涉及一般式I的化合物,其中R1选择自由基组成的群体中,该群体由-
CH2-Ra组成,其中Ra表示C1-6烷基,可选单烷基或多取代
氟,或C3-6环烷基,可选单烷基或多取代
氟,并可选择从
CH3,
CF3和
CHF2中选择的基团进行取代,以及Lp,(Het)Ar1,(Het)Ar2和n如申请中所定义,具有有价值的药理特性,特别是能够结合到GPR119受体并调节其活性。