HuagongsheHuagongshe Chemistry Print Report · For research reference only
Donepezil → 5,6-Dimethoxy-2-(4-pyridyl)methylene-1-indanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Donepezil | HCID 3152 | — |
| Reactant | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Reactant | 5,6-Dimethoxy-1-indanone | HCID 75018 | — |
| Product | 5,6-Dimethoxy-2-(4-pyridyl)methylene-1-indanone | HCID 53395132 | — |
Reaction Steps
U.S. Pat. No. 5,606,064 disclosed a process for the preparation of donepezil. 5,6-dimethoxy-1-indanone was condensed with pyridin-4-aldehyde to give 5,6-dimethoxy-2-(pyridin-4-yl)methyleneindan-1-one, reacted with benzyl bromide to give 1-benzyl-4-(5,6-dimethoxyindan-1-on-2-ylidene)methylpyridinium bromide and then, hydrogenated in the presence of platinum oxide catalyst to yield donepezil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07446203B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-55926d35552f411986f67c3cab95f973 |
| Source note | uspto-grants-2008_11 |