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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503379Generated: October 26, 2026

5-nitro-2-(pyridin-2-yl)-1H-indole → 2-(piperidin-2-yl)-1H-indol-5-amine

https://huagongshe.com/reaction/503379

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-nitro-2-(pyridin-2-yl)-1H-indoleHCID 59129380—
SolventHydrochloride methanolHCID 21893726—
Product2-(piperidin-2-yl)-1H-indol-5-amineHCID 59129471110.6%

Reaction Steps

5-Nitro-2-(pyridin-2-yl)-1H-indole (1.0 g, 4.2 mmol) was added to HCl/MeOH (2 M, 50 mL). The reaction mixture was stirred at room temperature for 1 h and the solvent was evaporated under vacuum. PtO2 (200 mg) was added to a solution of the residue in MeOH (50 mL) and the reaction mixture was stirred under hydrogen atmosphere (1 atm) at room temperature for 2 h. The catalyst was filtered through a celite pad and the solvent was evaporated under vacuum to afford 2-(piperidin-2-yl)-1H-indol-5-amine (1.0 g), which was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776905B2
Source datasetuspto-grants-2010_08
ORD IDord-f08a42db67db4adf875ba4a09f1d6fad
Source noteuspto-grants-2010_08