Triazolopyridine compounds

A compound of formula (I)

• wherein
• R1 is aryl, heteroaryl or NR4R5, wherein said aryl and said heteroaryl can be substituted by 1 to 3 substituents independently selected from the group consisting of hydroxyl, halogen, C1-C7 alkyl, C1-C7 alkoxy and C1-C7 haloalkyl;
• R2 is hydrogen, halogen or C1-C7 alkyl;
• R3 is aryl or heteroaryl, wherein said aryl and said heteroaryl can be substituted by 1 to 3 substituents independently selected from the group consisting of C1-C7 alkyl, hydroxyl, halogen, —C(O)—NR6R7 and —C(O)—O—R8;
• R4 and R5 are independently C1-C7 alkyl, C3-C8 cycloalkyl, together with the nitrogen atom to which they are attached, form a heterocycloalkyl which can be substituted by 1 to 3 substituents independently selected from the group consisting of hydroxyl, halogen, C1-C7 alkyl, C1-C7 alkoxy and C1-C7 haloalkyl;
• R6 and R7, are independently C1-C7 alkyl, C3-C8 cycloalkyl, together with the nitrogen atom to which they are attached, form a heterocycloalkyl which can be substituted by 1 to 3 substituents independently selected from the group consisting of hydroxyl, halogen, C1-C7 alkyl, C1-C7 alkoxy and C1-C7 haloalkyl;
• R8 is hydrogen, C1-C7 alkyl, cycloalkyl;
• or a pharmaceutically acceptable salt thereof.