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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 24482Erstellt: 24. Oktober 2026

Piperidine → 3-(3-methyl-1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acid

https://huagongshe.com/de/reaction/24482

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidineHCID 8082—
Edukt3-Methyl-1H-indole-2-carbaldehydeHCID 277260—
Edukt2-Oxindole-5-carboxylic acidHCID 2773318—
LösungsmittelEthanolHCID 702—
Produkt3-(3-methyl-1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acidHCID 5413855567%

Reaktionsschritte

A mixture of 5-carboxy-2-oxindole (113 mg), 3-methylindole-2-carbaldehyde (56 mg) (prepared according to Synthetic Communications, 1986, 16, 1799) 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 75 mg (58% yield) of 3-(3-methyl-1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acid (piperidine salt).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06855730B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-7fed27c586384673894442131d61abef
Quellennotizuspto-grants-2005_02