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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | 3-Methyl-1H-indole-2-carbaldehyde | HCID 277260 | — |
| Edukt | 2-Oxoindoline-5-sulfonamide | HCID 10198232 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 3-(3-methyl-1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide | HCID 53976496 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06680335B2 |
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| Quelldatensatz | uspto-grants-2004_01 |
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| ORD ID | ord-a77670fd823947dfa5be7e6cb08166e2 |
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| Quellennotiz | uspto-grants-2004_01 |
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