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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860877Generated: October 25, 2026

Piperidine → 5-methyl-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one

https://huagongshe.com/reaction/1860877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3-Methyl-1H-indole-2-carbaldehydeHCID 277260—
Reactant5-Methylindolin-2-oneHCID 5325716—
SolventEthanolHCID 702—
Product5-methyl-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydroindol-2-oneHCID 5375537874%

Reaction Steps

A mixture of 5-methyl-2-oxindole (59 mg), 3-methylindole-2-carbaldehyde (56 mg) and piperidine (30 mg) in ethanol (1 mL) was held in a sealed tube at 90° C. overnight. 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 72 mg (74%) of 5-methyl-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531502B1
Source datasetuspto-grants-2003_03
ORD IDord-a01f5b07acd74b7897aa2ba7aabb9758
Source noteuspto-grants-2003_03