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]>C(OCC)(=O)C.C(O)C>[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
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
0.3 g of Donepezil was dissolved in 3 ml of ethyl acetate under heating. Under stirring at room temperature, 0.79 ml of 10%-hydrogen chloride in ethanol solution was added. Filtration of the crystals and drying at 85° C. for 3 hours, then at 70° C. for 16 hours afforded 0.3g of the title compound.
Workup
- temperatureunder heating
- filtrationFiltration of the crystals
- customdrying at 85° C. for 3 hours
Sources & evidence
- ORD record
- ord-d3a2f401e2864739b4f87bb23cf02551
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05985864
Reaction notes
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