Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532622Generated: October 31, 2026

3-(4-Piperidinyl)-1H-indole → HCID 9908484, compound

https://huagongshe.com/reaction/1532622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Piperidinyl)-1H-indoleHCID 702235—
Reactant5-Fluoro-1-(2-oxiranylmethyl)-1H-indoleHCID 15524200—
ProductHCID 9908484HCID 990848451%

Reaction Steps

A methanolic solution of 1-N-glycidyl-5-fluoroindole (0.52 g, 3.0 mmole) from example 1 and 3-(4-piperidinyl)indole (0.6 g, 3.0 mmole) was refluxed under nitrogen for 15 hours. The reaction mixture was concentrated in vacuo and the product purified by flash silica gel chromatography (ethyl acetate) to afford the titled compound as an oil (0.599 g, 50% yield). Treatment with a 0.25 M ethanolic solution of fumaric acid (0.5 equivalents) gave the required product as a white solid. The product was recrystallized twice from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204274B1
Source datasetuspto-grants-2001_03
ORD IDord-33fc7a89a3cf4adf8eb53404b405dc76
Source noteuspto-grants-2001_03