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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003587Generated: October 30, 2026

HCID 18797135, compound → 2-(Piperidin-4-yl)-1H-indole

https://huagongshe.com/reaction/1003587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18797135HCID 18797135—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(Piperidin-4-yl)-1H-indoleHCID 1336089730%

Reaction Steps

A mixture of 0.521 gm (1.8 mMol) 2-(1-benzyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole and 0.1 gm 5% palladium on carbon were stirred together in ethanol under hydrogen (1 atm) for 48 hours. The reaction mixture was filtered through a bed of celite and the filtrate concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 20% methanol in dichloromethane containing a trace of ammonium hydroxide. Fractions containing product were combined and concentrated under reduced pressure to provide 0.107 gm (30%) 2-(piperidin-4-yl)-1H-indole as a light yellow solid. A portion of this material was treated with oxalic acid to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046215
Source datasetuspto-grants-2000_04
ORD IDord-e1021d023561439e94388f1b4c1d7718
Source noteuspto-grants-2000_04