HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methoxy-4-nitro-1-oxo-1lambda~5~-pyridine → 3-Methoxy-4-aminopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methoxy-4-nitro-1-oxo-1lambda~5~-pyridine | HCID 14762710 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Methoxy-4-aminopyridine | HCID 3016738 | — |
Reaction Steps
A solution of 3-methoxy-4-nitropyridine-N-oxide (17.37 g, 0.102 mol) in MeOH (180 ml) was hydrogenated in a 500 ml Parr bottle at 40° C. and 40 psi for 3 hours using Raney Nickel as catalyst. After filtration of the catalyst and evaporation of the solvent, the residue was chromatographed on silica gel using CH2Cl2 /MeOH/NH4OH (90/10/1) as the eluent to give the title compound. The product was recrystallized from toluene to give 10.8 g (65%) of pure product, m.p. 94°-95° C. The structural assignment is supported by the proton NMR spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05652363 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-7457f0086d1a48adbfe786d67aac15fe |
| Source note | uspto-grants-1997_07 |