摘要 |
The present invention is directed to compounds of formula (I): or a pharmaceutically acceptable salt thereof; wherein A is (II); X is selected from CH, CF and N, R8 is selected from H, C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl, aryl, heteroaryl, C<SUB>1</SUB>-C<SUB>6 </SUB>alkylaryl, C<SUB>1</SUB>-C<SUB>6 </SUB>alkylheteroaryl, C<SUB>2</SUB>-C<SUB>6 </SUB>alkyl-O-C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl, C<SUB>1</SUB>-C<SUB>6 </SUB>haloalkyl, hydroxy C<SUB>2</SUB>-C<SUB>6 </SUB>alkyl, -C(O)R9 and -SO<SUB>2</SUB>R9, or R7 and R8 combine to form (III), (IV); W is selected from CR1O and CR15, R1O is selected from H, halo, -C(O)NR13R14, C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl, aryl, heteroaryl, C<SUB>1</SUB>-C<SUB>6 </SUB>alkylaryl, C<SUB>1</SUB>-C<SUB>6 </SUB>alkylheteroaryl, C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl-O-C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl and hydroxy C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl; Het is a N-linked 5-membered heteroaryl ring optionally substituted with 1-3 substituents selected from methoxy, Cl, F, CH<SUB>3</SUB>, CF<SUB>3</SUB>, aryl, heteroaryl, C<SUB>1</SUB>-C<SUB>4 </SUB>alkylaryl or C<SUB>1</SUB>-C<SUB>4 </SUB>alkylheteroaryl, for use as inhibitors of the DPP-IV enzyme in the treatment or prevention of conditions including Type II diabetes.
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