2-(4-Chloro-butyl)-2H-[1,2,4]triazine-3,5-dione → HCID 42603370, compound
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][CH2:5][N:6]1[C:11](=[O:12])[NH:10][C:9](=[O:13])[CH:8]=[N:7]1.[C:14]([C:18]1[N:23]=[C:22]([N:24]2[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]2)[CH:21]=[C:20]([CH:30]2[CH2:33][CH2:32][CH2:31]2)[N:19]=1)([CH3:17])([CH3:16])[CH3:15]>>[C:14]([C:18]1[N:23]=[C:22]([N:24]2[CH2:25][CH2:26][N:27]([CH2:2][CH2:3][CH2:4][CH2:5][N:6]3[C:11](=[O:12])[NH:10][C:9](=[O:13])[CH:8]=[N:7]3)[CH2:28][CH2:29]2)[CH:21]=[C:20]([CH:30]2[CH2:33][CH2:32][CH2:31]2)[N:19]=1)([CH3:17])([CH3:15])[CH3:16]Participants
3
Procedure
2-{4-[4-(2-tert-Butyl-6-cyclobutyl-pyrimidin-4-yl)-piperazin-1-yl]butyl}-2H-[1,2,4]triazine-3,5-dione was prepared from 2-(4-chloro-butyl)-2H-[1,2,4]triazine-3,5-dione and 2-tert-butyl-4-piperazin-1-yl-6-cyclobutylpyrimidine by analogy to the process described in example 1.
Sources & evidence
- ORD record
- ord-2d05a020964642e6966641c24ac22dc9
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08492540B2
Reaction notes
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