1-Methylpiperazine → 5-Bromo-2-(4-methylpiperazin-1-yl)pyridine
Reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5](I)=[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]=[CH: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
The product is obtained analogously to Example 3.24a is from 1.5 g (5.28 mmol) 5-bromo-2-iodopyridine and 1.3 mL (11.7 mmol) N-methylpiperazine.
Workup
- customThe product is obtained analogously to Example 3.24a
Sources & evidence
- ORD record
- ord-570f9e1a30774626a68a85b244e42e84
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08618132B2
Reaction notes
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