Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Donepezil | HCID 3152 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Donepezil Hydrochloride | HCID 5741 | 96.4% |
Reaction Steps
50 g of donepezil was dissolved by stirring in 280 g of ethanol under heating, followed by adding 15.1 g of concentrated hydrochloric acid thereto at the internal temperature of 28° C. Then, it was cooled and continued stirring while keeping the internal temperature at about 25° C. Crystals started precipitating about 40 minutes after the concentrated hydrochloric acid was poured into the mixture. After the precipitation started, the mixture was stirred at the internal temperature of 25° C. for 18 hours and then cooled to the internal temperature of 9° C. The crystals were collected by filtration and dried about 4 hours after the cooling was started, to give 52.81 g of polymorphic crystal (III) of donepezil hydrochloride (yield: 96.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07479563B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-fcf6b4a72e9c473bbc2c71da1d9711d1 |
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| Source note | uspto-grants-2009_01 |
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