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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70069Generated: October 25, 2026

5-Nitroindole → 5-Aminoindole

https://huagongshe.com/reaction/70069

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-NitroindoleHCID 22523—
Reactant(4-Phenylpiperidin-1-yl)(3,4,5-trimethoxyphenyl)methanoneHCID 39582222—
SolventEthanolHCID 702—
Product5-AminoindoleHCID 7886792.5%

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822513B2
Source datasetuspto-grants-2014_09
ORD IDord-ed2f14d75d3b46958858df77ec7402b5
Source noteuspto-grants-2014_09