HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336797Erstellt: 23. Oktober 2026
Hydrochloric Acid → N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide
https://huagongshe.com/de/reaction/336797
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2,3-Dichloroquinoxaline | HCID 16659 | — |
| Edukt | Benzenesulfonamide, 3-nitro- | HCID 67138 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide | HCID 5007601 | — |
Reaktionsschritte
2,3-Dichloroquinoxaline (26.1 g, 131.1 mmol), m-Nitrobenzene sulfonamide (26.5 g, 131.1 mmol) and potassium carbonate (18.1 g, 131.1) were dissolved in anhydrous DMSO (500 mL). The reaction was heated to 150° C. for 2 h. The reaction mixture was poured into water (400 mL), followed by addition of 2M HCl (60 mL). The product was extracted with EtOAc (3×500 mL). The organic layers were combined and washed water (2×500 mL) and brine (2×500 mL). The product was then dried with sodium sulfate to give N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) m/z for C14H9ClN4O4S: 364.94, 366.97 (MH+)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08889664B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-3f417f4790b34ac1b597de3477d23e6f |
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| Quellennotiz | uspto-grants-2014_11 |
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