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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238513Generated: October 29, 2026

3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1H-indole → 3-(1-Methylpiperidin-4-yl)-1h-indol-5-amine

https://huagongshe.com/reaction/238513

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1H-indoleHCID 11334373—
SolventMethanolHCID 887—
Product3-(1-Methylpiperidin-4-yl)-1h-indol-5-amineHCID 11831220—

Reaction Steps

3-(1-Methyl-1,2,3,6-tetrahydro-pyridin-4-yl)-5-nitro-1H-indole (2.7 g, Step A) was dissolved in MeOH (50 mL), the mixture was bubbled with H2 for 10 min. 10% Pd/C (150 mg) was added and the mixture was stirred under H2 overnight. The mixture was filtered through Celite® and concentrated in vacuo to afford 3-(1-methyl-4-piperidyl)indole-5-ylamine as a yellow oil. MS: 230 (M+1). Calc'd. for C14H19N3—229.32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642624B2
Source datasetuspto-grants-2014_02
ORD IDord-09ca4920c1f54c8a99ba444f52f59aa4
Source noteuspto-grants-2014_02