一种合成新的多环骨架的有效方法:吡啶并[2',1':2,3]咪唑并[5,4 - c ]喹啉-6(5 H)-ones和吡啶并[2',1':2 ,3]咪唑并[5,4 - c ] azepin-7(6 H)-ones文库是通过Pd催化的涉及C(sp2)-H活化的分子内芳基化进行描述的。该方法允许以高收率合成多环衍生物。该方法耐受各种芳基取代基以及烷基咪唑并[1,2 - a ]吡啶-2-羧酰胺结构。在Suzuki交叉偶联条件下将所得化合物10(11)-氯-吡啶并[2',1':2,3]咪唑并[5,4- c ]喹啉酮或氮杂环庚烷酮官能化以得到多官能化合物。
Phenoxymethyl compounds that inhibit at least one phosphodiesterase 10 are described as are pharmaceutical compositions containing such compounds an methods for treating various CNS disorders by administering such compounds to a patient in need thereof.
Phenoxymethyl compounds that inhibit at least one phosphodiesterase 10 are described as are pharmaceutical compositions containing such compounds an methods for treating various CNS disorders by administering such compounds to a patient in need thereof.