2-Tert-butyl-4-[4-(3-chloropropyl)piperazin-1-yl]-6-(trifluoromethyl)pyrimidine → 2-tert-Butyl-4-{4-[3-(4-methyl-5-methyl-4H-[1,2,4]triazol-3-ylsulfanyl)-propyl]-piperazin-1-yl}-6-trifluoromethyl-pyrimidine hydrochloride
反応式
[CH3:1][N:2]1[C:6]([CH3:7])=[N:5][N:4]=[C:3]1[SH:8].[C:9]([C:13]1[N:18]=[C:17]([N:19]2[CH2:24][CH2:23][N:22]([CH2:25][CH2:26][CH2:27][Cl:28])[CH2:21][CH2:20]2)[CH:16]=[C:15]([C:29]([F:32])([F:31])[F:30])[N:14]=1)([CH3:12])([CH3:11])[CH3:10]>>[ClH:28].[C:9]([C:13]1[N:18]=[C:17]([N:19]2[CH2:24][CH2:23][N:22]([CH2:25][CH2:26][CH2:27][S:8][C:3]3[N:2]([CH3:1])[C:6]([CH3:7])=[N:5][N:4]=3)[CH2:21][CH2:20]2)[CH:16]=[C:15]([C:29]([F:30])([F:31])[F:32])[N:14]=1)([CH3:10])([CH3:11])[CH3:12]参加物
3
実験手順
3 g of 4-methyl-5-methyl-4H-[1,2,4]triazole-3-thiol (23.22 mmol) were reacted with 8.47 g of 2-tert-butyl-4-[4-(3-chloro-propyl)-piperazin-1-yl]-6-trifluoromethyl-pyrimidine (23.22 mmol) to yield 8.7 g of the title compound.
出典と根拠
- ORDレコード
- ord-0f5eb6a67cde4dd19248a94b0e222733