Hydrochloric Acid → 2-{3-[4-(4-bromo-2-methoxyphenyl)piperazin-1-yl]propylamino}-N,N-dimethylnicotinamide hydrochloride
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][CH2:16][NH:17][C:18]3[N:28]=[CH:27][CH:26]=[CH:25][C:19]=3[C:20]([N:22]([CH3:24])[CH3:23])=[O:21])[CH2:10][CH2:9]2)=[C:4]([O:29][CH3:30])[CH:3]=1.[ClH:31]>C(Cl)Cl.CO>[ClH:31].[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:9][CH2:10][N:11]([CH2:14][CH2:15][CH2:16][NH:17][C:18]3[N:28]=[CH:27][CH:26]=[CH:25][C:19]=3[C:20]([N:22]([CH3:24])[CH3:23])=[O:21])[CH2:12][CH2:13]2)=[C:4]([O:29][CH3:30])[CH:3]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
The 2-{3-[4-(4-bromo-2-methoxyphenyl)piperazin-1-yl]propylamino}-N,N-dimethylnicotinamide (0.19 g, 0.40 mmol) was dissolved in methylene chloride and the solution was treated with excess hydrochloric acid in methanol and concentrated to dryness. The residue was triturated with ethyl acetate and dried to give 2-{3-[4-(4-bromo-2-methoxyphenyl)piperazin-1-yl]propylamino}-N,N -dimethylnicotinamide hydrochloride. Anal.: Calcd. for C22H30 BrN5O2.(HCl)2.H2O: C, 46.96; H, 6.37; N, 11.60%; Found: C, 46.56H, 6.37; N, 11.60%.
Workup
- concentrationconcentrated to dryness
- customThe residue was triturated with ethyl acetate
- customdried
Sources & evidence
- ORD record
- ord-aa7790bc74c049e599b1cf733a5b6a02
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05688795
Reaction notes
Loading…