Reacción #359067
ord-2e4f46fc488443e19b00066e91b15bb3
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1TemperaturaThe solution was cooled
- 2Otropurged with argon, and 10% palladium on carbon
- 3workup.ADDITIONwas added (0.45 g)
- 4workup.ADDITIONHydrogen was introduced (1 atm)
- 5FiltraciónThe catalyst was filtered
- 6Otrothe solvent evaporated from the filtrate
Procedimiento
2-Amino-6-methoxy-3-nitropyridine (2.8 g, 16.5 mmol) was dissolved in warm 1:1 methanol/ethanol (200 mL). The solution was cooled, purged with argon, and 10% palladium on carbon was added (0.45 g). Hydrogen was introduced (1 atm) and the reaction stirred until complete. The catalyst was filtered and the solvent evaporated from the filtrate to give the title compound. MS 140 (M+1) 1H NMR (500 MHz, CDCl3) δ 6.93 (d, J=8 Hz, 1H), 6.04 (d, J=8 Hz, 1H), 4.15 (br s, 2H), 3.80 (s, 3H), 3.0 (br s, 2H).