1-Methylpiperazine → 5-Bromo-2-(4-methylpiperazin-1-yl)pyrimidine
Reaction equation
[Br:1][C:2]1[CH:3]=[N:4][C:5](Cl)=[N:6][CH:7]=1.[CH3:9][N:10]1[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]1>>[Br:1][C:2]1[CH:3]=[N:4][C:5]([N:13]2[CH2:14][CH2:15][N:10]([CH3:9])[CH2:11][CH2:12]2)=[N:6][CH:7]=1Participants
3
Procedure
Following the procedure described for Intermediate 234 using 5-bromo-2-chloropyrimidine and N-methylpiperazine provided the title compound. ESMS [M+H]+: 257.0/259.0.
Sources & evidence
- ORD record
- ord-c94ac27cf53343b79231087a32710cf0
- Source dataset
- uspto-grants-2009_02
- Patent number
- US07495102B2
Reaction notes
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