HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1814092Erstellt: 25. Oktober 2026
1,4-Dioxane → 1-Benzenesulfonyl-5-methanesulfonyl-2-(3-pyridyl)indole
https://huagongshe.com/reaction/1814092
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Edukt | Potassium Acetate | HCID 517044 | — |
| Edukt | 3-(Trimethylsilylethynyl)pyridine | HCID 4100857 | — |
| Edukt | 1-Benzenesulfonylamino-2-iodo-4-methanesulfonylbenzene | HCID 22504376 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-Benzenesulfonyl-5-methanesulfonyl-2-(3-pyridyl)indole | HCID 22504414 | 63% |
Reaktionsschritte
A mixture of 3-trimethylsilylethynylpyridine (1.07 g), 2-benzenesulfonylamino-3-iodo-5-methanesulfonylbenzene (1.75 g), potassium acetate (1.60 g), cuprous iodide (60 mg), dichlorobis(triphenylphosphine)palladium (0.20 g) and 1,4-dioxane (4 ml) was stirred at 100° C. for 12 hours under nitrogen atmosphere. To the reaction solution were added water and ethyl acetate. The insolubles were filtered off. The filtrate was extracted with ethyl acetate, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (hexane:ethyl acetate=1:3) to obtain 1.04 g of the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06875770B2 |
|---|
| Quelldatensatz | uspto-grants-2005_04 |
|---|
| ORD ID | ord-fc99351053ee40dc8d49b302f8fd0440 |
|---|
| Quellennotiz | uspto-grants-2005_04 |
|---|