2-(tert-Butyl)-4-(piperazin-1-yl)-6-(trifluoromethyl)pyrimidine → 2-{4-[4-(2-tert-Butyl-6-trifluoromethyl-pyrimidin-4-yl)-piperazin-1-yl]-butyl}-6-methyl-2H-[1,2,4]triazine-3,5-dione hydrochloride
Reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][N:6]1[C:11](=[O:12])[NH:10][C:9](=[O:13])[C:8]([CH3:14])=[N:7]1.[C:15]([C:19]1[N:24]=[C:23]([N:25]2[CH2:30][CH2:29][NH:28][CH2:27][CH2:26]2)[CH:22]=[C:21]([C:31]([F:34])([F:33])[F:32])[N:20]=1)([CH3:18])([CH3:17])[CH3:16]>>[ClH:1].[C:15]([C:19]1[N:24]=[C:23]([N:25]2[CH2:26][CH2:27][N:28]([CH2:2][CH2:3][CH2:4][CH2:5][N:6]3[C:11](=[O:12])[NH:10][C:9](=[O:13])[C:8]([CH3:14])=[N:7]3)[CH2:29][CH2:30]2)[CH:22]=[C:21]([C:31]([F:32])([F:33])[F:34])[N:20]=1)([CH3:18])([CH3:16])[CH3:17]Participants
3
Reactant 2
Product 1
Procedure
2-{4-[4-(2-tert-Butyl-6-trifluoromethyl-pyrimidin-4-yl)-piperazin-1-yl]-butyl}-6-methyl-2H-[1,2,4]triazine-3,5-dione hydrochloride was prepared from 2-(4-chloro-butyl)-6-methyl-2H-[1,2,4]triazine-3,5-dione and 2-tert-butyl-4-piperazin-1-yl-6-trifluoromethyl-pyrimidine by analogy to the process described in example 1.
Sources & evidence
- ORD record
- ord-17d582121b2b464a8eee993d8e1c038d
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08492540B2
Reaction notes
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