HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1840487Erstellt: 24. Oktober 2026
Piperidine → 3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide
https://huagongshe.com/de/reaction/1840487
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | Indole-2-carboxaldehyde | HCID 96389 | — |
| Edukt | 2-Oxoindoline-5-sulfonamide | HCID 10198232 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide | HCID 54232128 | 83% |
Reaktionsschritte
A mixture of 5-aminosulfonyl-2-oxindole (106 mg) (prepared as described in Compound IN-02), indole-2-carbaldehyde (87 mg) (prepared according to Synthetic Communications, 1993, 23, 3109) and piperidine (4 mg) in ethanol (2 mL) was heated in a sealed tube at 90° C. for 3 hours. 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 140 mg (83% yield) of 3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide as an orange solid.
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-6e454b9f1c7848cc8c88aa3574f4c59a |
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| Quellennotiz | uspto-grants-2004_01 |
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