N-(3,4-dimethoxybenzyl)-N-[thieno[2,3-d]pyrimidin-6-ylmethylidene]amine → 6-[1-(3,4-Dimethoxybenzyl)-4-phenyl-1H-imidazol-5-yl]-4-(methylthio)thieno[2,3-d]pyrimidine
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:20]=[CH:21][C:22]=1[O:23][CH3:24])[CH2:6][N:7]=[CH:8][C:9]1[S:19][C:12]2[N:13]=[CH:14][N:15]=[C:16]([S:17][CH3:18])[C:11]=2[CH:10]=1.CO[C:27]1[CH:28]=[C:29]([CH:42]=[CH:43][C:44]=1OC)[CH2:30][N:31]=[CH:32]C1SC2N=CN=CC=2C=1>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:20]=[CH:21][C:22]=1[O:23][CH3:24])[CH2:6][N:7]1[C:8]([C:9]2[S:19][C:12]3[N:13]=[CH:14][N:15]=[C:16]([S:17][CH3:18])[C:11]=3[CH:10]=2)=[C:30]([C:29]2[CH:42]=[CH:43][CH:44]=[CH:27][CH:28]=2)[N:31]=[CH:32]1参加物
3
反応物 2
生成物 1
実験手順
The title compound was prepared in 55% yield using a procedure similar to the one described for example 6 above but starting from N-(3,4-dimethoxybenzyl)-N-{[4-(methylthio)thieno[2,3-d]pyrimidin-6-yl]methylidene}amine (intermediate 18) (76 mg), in place of N-(3,4-dimethoxybenzyl)-N-[thieno[2,3d]pyrimidin-6-ylmethylidene]amine (intermediate 14);