HuagongsheHuagongshe Chemistry Print Report · For research reference only
Deferiprone → 1-Ethyl-3-hydroxy-2-methyl-4-pyridinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Deferiprone | HCID 2972 | — |
| Reactant | Ethylamine | HCID 6341 | — |
| Product | 1-Ethyl-3-hydroxy-2-methyl-4-pyridinone | HCID 94413 | — |
Reaction Steps
A reaction analogous to that used for the synthesis of 3-hydroxy-1,2-dimethyl-4-pyridinone was employed, starting with 70% ethylamine (4.6 g). No precipitate was observed after concentration. Recrystallization from ethanol and diethyl ether resulted in a white powder (4.2 g). Proton NMR (D20): 7.85 (d, 1H), 6.88 (d, 1H), 4.12 (q, 2H), 2.36 (s, 3H), 1.24 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06294152B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-8ccafc82b50f429398ab95a8a8a32f95 |
| Source note | uspto-grants-2001_09 |