HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 731140Erstellt: 25. Oktober 2026
5-fluoro-1,3-dihydro-2H-indol-2-one → 5-(5-Fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid
https://huagongshe.com/reaction/731140
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 5-fluoro-1,3-dihydro-2H-indol-2-one | HCID 3731012 | — |
| Edukt | 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic Acid | HCID 11073792 | — |
| Katalysator | Piperidine | HCID 8082 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 5-(5-Fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid | HCID 53395102 | 101,4% |
Reaktionsschritte
The reaction mixture of 5-fluorooxindole (100 mg, 0.66 mmol), 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (133 mg, 0.79 mmol), and 10 drops of piperidine in ethanol (3 mL) was stirred at 60° C. overnight and filtered. The solid washed with 1 M of aqueous hydrochloride solution, water, and dried to afford 5-(5-fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (201 mg, quantitative) as a yellow solid. MS m/z (relative intensity, %) 299 ([M−1]+., 100).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07582756B2 |
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| Quelldatensatz | uspto-grants-2009_09 |
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| ORD ID | ord-2789bc4114c74925a27d432d038a0eb3 |
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| Quellennotiz | uspto-grants-2009_09 |
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