HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 345663Erstellt: 24. Oktober 2026
Arcyriarubin A → 3,4-bis(1H-indol-3-yl)-2,5-dihydro-1H-pyrrol-2-one
https://huagongshe.com/de/reaction/345663
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Arcyriarubin A | HCID 2399 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3,4-bis(1H-indol-3-yl)-2,5-dihydro-1H-pyrrol-2-one | HCID 5327650 | 18,3% |
Reaktionsschritte
20 ml of a 1M solution of LiAlH4 in diethyl ether was added to a solution of 1.0 g of 3,4-bis(3-indolyl)-1H-pyrrole-2,5-dione in 140 ml of THF. The mixture was stirred for 18 hours under nitrogen. The mixture was cooled to 0° C., quenched with 50 ml of water, then acidified to pH 2 with 2M hydrochloric acid and extracted with ethyl acetate. The organic extracts were washed with saturated sodium bicarbonate solution, dried and evaporated. The residue was purified on silica gel with 5-10% methanol in dichloromethane. The first product eluted was triturated with ethyl acetate/hexane to give 175 mg of 3,4-bis(3-indolyl)-3-pyrrolin-2-one, m.p. 290°-293° C. (decomposition). The second product eluted was crystallized from ethyl acetate/chloroform to give 490 mg of 5-hydroxy-3,4-bis(3-indolyl)-3-pyrrolin-2-one, m.p. above 250° C. (decomposition).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05057614 |
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| Quelldatensatz | uspto-grants-1991_10 |
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| ORD ID | ord-4f5b573773694b3ca8ac6ab6160a6328 |
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| Quellennotiz | uspto-grants-1991_10 |
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