HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1838340Erstellt: 25. Oktober 2026
Water → 2-(2-Tetrahydrofuranyl)-5-methanesulfonyl-1-benzenesulfonylindole
https://huagongshe.com/reaction/1838340
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-Ethynyloxolane | HCID 10034582 | — |
| Edukt | 1-Benzenesulfonylamino-2-iodo-4-methanesulfonylbenzene | HCID 22504376 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 2-(2-Tetrahydrofuranyl)-5-methanesulfonyl-1-benzenesulfonylindole | HCID 22504449 | 91,8% |
Reaktionsschritte
To a solution of 1-benzenesulfonylamino-2-iodo-4-methanesulfonylbenzene (256 mg) in 1,4-dioxane (6 ml), 2-ethynyltetrahydrofuran (169 mg), bistriphenylphosphine palladium dichloride (21 mg), cuprous iodide (11 mg) and triethylamine (89 mg) were added successively and the mixture was stirred in a sealed tube at 60° C. for 3 hours. After cooling, the reaction solution was poured into water, extracted with dichloromethane, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel preparative thin-layer chromatography (hexane:ethyl acetate=1:1) to obtain 218 mg of the desired product in a white amorphous form.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06673797B1 |
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| Quelldatensatz | uspto-grants-2004_01 |
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| ORD ID | ord-69ea4f2f131c4410be81dd751da3a87c |
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| Quellennotiz | uspto-grants-2004_01 |
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