| 摘要 |
<p>The present invention concerns novel oxadiazole derivatives of formula (I), the <u>N</u>-oxide forms, the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof, wherein R1 is hydrogen or halo; R2 is C1-6alkyl, C2-6alkenyl or C2-6alkynyl; R3 is hydrogen; or R2 and R3 taken together may form a C2-3alkanediyl radical wherein one or two hydrogen atoms may be replaced by C1-4alkyl; R4 is hydrogen or C1-6alkyloxy; X is a bivalent radical of formula (a-1), or (a-2), L is a radical of formula -Alk-R5 or -Alk-O-R6, Alk is C1-12alkanediyl; R5 is hydrogen, cyano, C1-6alkylcarbonyl, C1-6alkylsulfinyl, C1-6alkylsulfonyl, aryl, arylcarbonyl, tetrahydrofuran, dioxolane, dioxolane substituted with C1-6alkyl, dioxane, dioxane substituted with C1-6alkyl; R6 is hydrogen, aryl, C1-6alkyl, hydroxyC1-6alkyl, C1-6alkylcarbonyl; aryl is defined as phenyl or phenyl substituted with up to three substituents selected from halo, C1-6alkyl or C1-6alkyloxy. It further relates to pharmaceutical compositions comprising them, processes for preparing said compounds and compositions, and the use thereof as a medicine, in particular in the conditions involving a decreased motility of the colon.</p> |
