Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24495Generated: October 25, 2026

Piperidine → HCID 54279577, compound

https://huagongshe.com/reaction/24495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant5-ChlorooxindoleHCID 152801—
Reactant3-Methyl-1H-indole-2-carbaldehydeHCID 277260—
SolventEthanolHCID 702—
ProductHCID 54279577HCID 54279577—

Reaction Steps

A mixture of 5-chloro-2-oxindole (167 mg), 3-methylindole-2-carbaldehyde (190 mg) (prepared according to Synthetic Communications, 1986, 16, 1799) and piperidine (10 mg) in ethanol was held in a sealed tube at 95° C. for 4 hours. The mixture was cooled to room temperature. The solid was collected by vacuum filtration, washed with cold ethanol and dried in a vacuum oven to give 5-chloro-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855730B2
Source datasetuspto-grants-2005_02
ORD IDord-0f0956a71f69423faf28213214a60c00
Source noteuspto-grants-2005_02