HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53747Erstellt: 24. Oktober 2026
hydroxylamine-O-sulfonic acid → 1-Amino-5,7-dichloro-1,4-dihydro-2,3-quinoxalinedione
https://huagongshe.com/de/reaction/53747
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | hydroxylamine-O-sulfonic acid | HCID 76284 | — |
| Edukt | 5,7-Dichloro-1,4-dihydroquinoxaline-2,3-dione | HCID 650260 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Potassium Hydroxide | HCID 14797 | — |
| Produkt | 1-Amino-5,7-dichloro-1,4-dihydro-2,3-quinoxalinedione | HCID 19958618 | 69% |
Reaktionsschritte
The procedure of Wallace, R. G., Org. Prep. Proc. Int. 14: 269 (1982) was adapted. 5,7-Dichloro-1,4-dihydroquinoxaline-2,3-dione (52 mg, 0.225 mmole) was dissolved in 3N KOH (1 mL) at 60° C. for 0.5 h, and NH2OSO3H (30 mg, 0.265 mmole, Aldrich) in distilled water (0.5 mL) was dropwise added into above solution with stirring at 60° C. Some precipitate came out after 15 mins. The mixture was stirred at room temperature overnight. The white precipitate was collected by filtration, washed with cold distilled water (0.5 mL) and dried on rotavapor at 60° C. for 2 h affording crude 1-amino-5,7-dichloro-1,4-dihydro-2,3-quinoxalinedione (38 mg, 69%), which included a little of the isomer (4-amino-5,7-dichloro-2,3-quinoxalinedione) by 1H NMR (it is not known which isomer is present in a greater amount).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05620979 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-4c5d952d5e704bfdac91a8ae748464b9 |
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| Quellennotiz | uspto-grants-1997_04 |
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