1-Ethylpiperazine → 6-(4-Ethylpiperazin-1-yl)nicotinamide
Reaction equation
Cl[C:2]1[CH:27]=[CH:26][C:5]([C:6]([NH:8]C2C=CC(Cl)=C(NC(=O)C3C=CC=C(Cl)C=3)C=2)=[O:7])=[CH:4][N:3]=1.[CH2:28]([N:30]1[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]1)[CH3:29]>>[CH2:28]([N:30]1[CH2:35][CH2:34][N:33]([C:2]2[CH:27]=[CH:26][C:5]([C:6]([NH2:8])=[O:7])=[CH:4][N:3]=2)[CH2:32][CH2:31]1)[CH3:29]Participants
3
Procedure
6-chloro-N-(4-chloro-3-(3-chlorobenzamido)phenyl)nicotinamide (0.16 mmol) was used in general procedure 3 with 1-ethylpiperazin (0.83 mmol). The product was purified by RP-HPLC to give N-(4-chloro-3-(3-chlorobenzamido)phenyl))-6-(4-ethylpiperazin-1-yl)nicotinamide. MS (Q1) 498.1 (M)+
Workup
- customThe product was purified by RP-HPLC
Sources & evidence
- ORD record
- ord-9cb838b272034a5aa9aed247980aafd7
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08101610B2
Reaction notes
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