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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1840477Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1840477

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidineHCID 8082—
Edukt3-Methyl-1H-indole-2-carbaldehydeHCID 277260—
Edukt2-Oxoindoline-5-sulfonamideHCID 10198232—
LösungsmittelEthanolHCID 702—
Produkt3-(3-methyl-1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amideHCID 5397649671%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of 5-aminosulfonyl-2-oxindole (84 mg), 3-methylindole-2-carbaldehyde (56 mg) (prepared according to Synthetic Communications, 1986, 16, 1799) and piperidine (30 mg) in ethanol (1 mL) was heated in a sealed tube at 90° C. for overnight. The mixture was cooled to room temperature. The solid was collected by vacuum filtration, washed with cold ethanol and dried in oven for overnight to give 88 mg (71% yield) of 3-(3-methyl-1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06680335B2
Quelldatensatzuspto-grants-2004_01
ORD IDord-a77670fd823947dfa5be7e6cb08166e2
Quellennotizuspto-grants-2004_01