HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Napthylmethylaminopyridone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromomethylnaphthalene | HCID 70320 | — |
| Reactant | 3-Amino-5-ethyl-6-methyl-1H-pyridin-2-one | HCID 481022 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Napthylmethylaminopyridone | HCID 53893567 | 47.9% |
Reaction Steps
A mixture of 3-amino-5-ethyl-6-methyl-2-(1H)-pyridinone (3.0 g, 20 mmol), 2-bromomethylnapthalene (4.4 g, 20 mmol), triethylamine (2.0 g, 20 mmol) in acetonitrile (200 mL) was heated under reflux for 4 hours. The resultant mixture was allowed to cool to room temperature and concentrated under reduced pressure (15 torr). The residue was then subjected to column chromatography on silica gel (300 g, elution with methanol-chloroform, 5:95 v/v). Collection and concentration of appropriate fractions provided 2.4 g (42%) of the napthylmethylaminopyridone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05308854 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-eef5d0e6cfba422ca871ffaa9288b788 |
| Source note | uspto-grants-1994_05 |