Thienopyrimidine derivatives, processes for the preparation thereof and therapeutic uses thereof

A compound of formula (II):

• wherein:
• R7 is an aryl group or a heteroaryl group, wherein the aryl group or the heteroaryl group is optionally substituted with one or several substituents selected, independently in each instance, from the group consisting of cyano, halogen, (C1-C6)alkyl, OR′4, CH2OH, CH2NH2, S(O)nR′4, R8 and OR8;
• wherein:
• R′4 is a hydrogen atom, a (C1-C6)alkyl group or an aryl group, wherein the (C1-C6)alkyl group or the aryl group is optionally substituted with a halogen atom, an NH2 group or an OH group;
• n is 1 or 2;
• and
• R8 is a halo(C1-C6)alkyl group;
• and
• R16 is a (C1-C6)alkoxy group;
• or a pharmaceutically acceptable salt thereof.