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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 522593Erstellt: 25. Oktober 2026

5-Nitroindole → 5-Aminoindole

https://huagongshe.com/reaction/522593

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-NitroindoleHCID 22523—
Edukt(4-Phenylpiperidin-1-yl)(3,4,5-trimethoxyphenyl)methanoneHCID 39582222—
LösungsmittelEthanolHCID 702—
Produkt5-AminoindoleHCID 7886792,5%

Reaktionsschritte

A mixture of 5-nitro-1H-indole (11 g, 67.9 mmol) and Pd/C (5%; 1g), dissolved in ethanol (50 mL), was hydrogenated for 3 h at 40 psi. The reaction mixture was filtered and the excess of ethanol was evaporated under reduced pressure. Solid product was recrystallized from hexane to obtain the pure compound 5-aminoindole (55-1). Yield: 92.5%. 1H NMR (500 MHz, CDCl3): δ 7.96 (br, 1H), 7.20 (d, 1H), 7.13 (s, 1H), 6.95 (s, 1H), 6.67 (dd, 1H), 6.37 (s, 1H), 3.50 (s, 2H). MS (ESI) m/z 133.0 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09334242B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-71544049c5fb4b0f8a0df2fa57ccf873
Quellennotizuspto-grants-2016_05