[CH3:1][N:2]1[C:6](N)=[CH:5][CH:4]=[N:3]1.[CH2:8]([O:10][C:11]1[CH:16]=[C:15]([NH2:17])[CH:14]=[CH:13][N:12]=1)[CH3:9]>>[CH2:8]([O:10][C:11]1[CH:16]=[C:15]([NH:17][C:1]2[N:3]=[CH:4][C:5]3[CH2:5][CH2:6][NH:2][CH2:1][C:6]=3[N:2]=2)[CH:14]=[CH:13][N:12]=1)[CH3:9]N-(2-ethoxypyridin-4-yl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-amine (186) was prepared in accord with the procedures described in steps 1 to 4 of example 25 except in step 1, 1-methyl-1H-pyrazol-5-amine was replaced with 2-ethoxypyridin-4-amine.
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