Reacción #1962001
ord-a8f6ec24f800483090ffc2f5fa76827b
Ecuación de reacción
ethyl 7-nitro-1H-indole-2-carboxylate
→
title compound
ethyl 7-amino-1H-indole-2-carboxylate
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroThe mixture was evacuated
- 2Otroflushed with nitrogen three times
- 3Otroflushed with hydrogen (60 psi)
- 4Otroevacuated three times
- 5workup.ADDITIONfilled with hydrogen (60 psi)
- 6Filtraciónthe reaction mixture was filtered through celite
- 7ConcentraciónThe filtrate was concentrated
- 8Otrothe residue was purified by column chromatography (hexane/EtOAc)
Procedimiento
Platinum(IV) oxide (0.024 g, 0.107 mmol) was added to a suspension of ethyl 7-nitro-1H-indole-2-carboxylate (0.10 g, 0.30 mmol) in ethanol (20 mL) in a Fisher-Porter vessel. The mixture was evacuated and flushed with nitrogen three times, flushed with hydrogen (60 psi) and evacuated three times, then filled with hydrogen (60 psi). After 30 min, the reaction mixture was filtered through celite. The filtrate was concentrated and the residue was purified by column chromatography (hexane/EtOAc) to give the title compound (0.324 g, 74%) as a yellow solid. 1H NMR (400 MHz, CDCl3): δ ppm 9.60 (s, 1H), 7.22 (d, 1H), 7.19 (d, 1H), 6.94-7.03 (m, 1H), 6.66 (d, 1H), 4.43 (q, 2H), 1.44 (t, 3H). MS: m/z 205 (M+1).