Hydrochloric Acid → Donepezil Hydrochloride
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[CH2:14][CH:13]([CH2:15][CH:16]3[CH2:21][CH2:20][N:19]([CH2:22][C:23]4[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=4)[CH2:18][CH2:17]3)[C:11](=[O:12])[C:6]2=[CH:7][C:8]=1[O:9][CH3:10].[ClH:29]>C1(C)C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[CH2:14][CH:13]([CH2:15][CH:16]3[CH2:17][CH2:18][N:19]([CH2:22][C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)[CH2:20][CH2:21]3)[C:11](=[O:12])[C:6]2=[CH:7][C:8]=1[O:9][CH3:10].[ClH:29]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.0 g of Donepezil was dissolved in 30 ml of toluene at 20° C. Hydrogen chloride gas was blown hereinto at room temperature, until the atmosphere turns acidic. Argon gas was blown hereinto. After stirring for 30 minutes, filtration of the separated crystals followed by drying afforded 2.21 g of the title compound. (water content: 0.65%)
Workup
- customwas blown hereinto at room temperature, until the atmosphere
- filtrationfiltration of the separated crystals
- customby drying
Sources & evidence
- ORD record
- ord-59bd5105d565402fa7dcc4d3844e14cc
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05985864
Reaction notes
Loading…