HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[(6-Methoxypyridin-2-yl)methyl]acetamide → (6-Methoxypyridin-2-yl)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[(6-Methoxypyridin-2-yl)methyl]acetamide | HCID 13882972 | — |
| Reactant | (6-Methoxypyridin-2-yl)methanamine hydrochloride | HCID 13882974 | — |
| Reactant | 6-(Aminomethyl)pyridin-2(1H)-one hydrochloride | HCID 21243522 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | (6-Methoxypyridin-2-yl)methanamine | HCID 13882973 | — |
Reaction Steps
The crude product, 2-acetamidomethyl-6-methoxypyridine from Example 1, was combined with 10 ml of 6N hydrochloric acid, and the resulting mixture was heated at its reflux temperature for about 16 hours. The mixture was evaporated to provide a tan solid residue. The product was determined by infrared and nuclear magnetic resonance spectral analyses to be a mixture of 2-aminomethyl-6-methoxypyridine hydrochloride and 6-aminomethyl-2(1H)-pyridone hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04824953 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-306c57f94a7d4a41b0120d423dc9cc8d |
| Source note | uspto-grants-1989_04 |