Hydrochloric Acid → 1-(3,4,5-Trimethoxycinnamoyl)-4-[1-(isopropylaminocarbonyl)ethyl]piperazine Hydrochloride
Reaction equation
[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[C:6]([CH:25]=[C:26]([O:30][CH3:31])[C:27]=1[O:28][CH3:29])[CH:7]=[CH:8][C:9]([N:11]1[CH2:16][CH2:15][N:14]([CH:17]([C:19]([NH:21][CH:22]([CH3:24])[CH3:23])=[O:20])[CH3:18])[CH2:13][CH2:12]1)=[O:10]>C(O)C>[ClH:1].[CH3:31][O:30][C:26]1[CH:25]=[C:6]([CH:5]=[C:4]([O:3][CH3:2])[C:27]=1[O:28][CH3:29])[CH:7]=[CH:8][C:9]([N:11]1[CH2:16][CH2:15][N:14]([CH:17]([C:19]([NH:21][CH:22]([CH3:24])[CH3:23])=[O:20])[CH3:18])[CH2:13][CH2:12]1)=[O:10]Participants
4
Procedure
3 ml of 15% ethanolic hydrogenchloride is added to a solution of 3.00 g of 1-(3,4,5-trimethoxycinnamoyl)-4-[1-(isopropylaminocarbonyl)ethyl]piperazine prepared as in Example 3 in 5 ml of ethanol, and the solvent is distilled off. Isopropanol is added to the abtained residue and the precipitates are collected by filtration.
Workup
- distillationthe solvent is distilled off
- additionIsopropanol is added to the abtained residue
- filtrationthe precipitates are collected by filtration
Sources & evidence
- ORD record
- ord-50125aaf1ec94dc5bcf46cee6f194dd8
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04478838
Reaction notes
Loading…