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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1840479Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1840479

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidineHCID 8082—
Edukt3-Methyl-1H-indole-2-carbaldehydeHCID 277260—
EduktN-methyl-2-oxoindoline-5-sulfonamideHCID 10176909—
LösungsmittelEthanolHCID 702—
Produkt3-(3-methyl-1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid methylamideHCID 5456508270%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of 5-methylaminosulfonyl-2-oxindole (90 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 90 mg (70% yield) of 3-(3-methyl-1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid methylamide (mixture of isomers).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06680335B2
Quelldatensatzuspto-grants-2004_01
ORD IDord-9dcaf09da6084b1dacc6d3ce33d6b17d
Quellennotizuspto-grants-2004_01