Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457841Generated: November 2, 2026

5-Methoxyindole → 5-Methoxy-3-(piperidin-4-yl)-1H-indole

https://huagongshe.com/reaction/457841

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-MethoxyindoleHCID 13872—
Reactant4-PiperidoneHCID 33721—
CatalystAdams' catalystHCID 345198—
Product5-Methoxy-3-(piperidin-4-yl)-1H-indoleHCID 4322474%

Reaction Steps

This compound was prepared following the procedure described in example 1 (parts A and B) starting with 5.9 g (40 mmol) of 5-methoxyindol and 15.5 g (100 mmol) of 4-piperidone. In this case the hydrogenation took place for 24 hours at 30 psi and the catalyst used was platinum (IV) oxide. 6.8 g (74% of yield) of 5-methoxy-3-piperidin-4-yl-1H-indole were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189741B2
Source datasetuspto-grants-2007_03
ORD IDord-ec2ee785a40c45e881fc369aa5a5b091
Source noteuspto-grants-2007_03