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HRID 54335Erstellt: 24. Oktober 2026

hydroxylamine-O-sulfonic acid → 1-Amino-5,7-dichloro-1,4-dihydro-2,3-quinoxalinedione

https://huagongshe.com/de/reaction/54335

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukthydroxylamine-O-sulfonic acidHCID 76284—
Edukt5,7-Dichloro-1,4-dihydroquinoxaline-2,3-dioneHCID 650260—
LösungsmittelWaterHCID 962—
LösungsmittelPotassium HydroxideHCID 14797—
Produkt1-Amino-5,7-dichloro-1,4-dihydro-2,3-quinoxalinedioneHCID 1995861869%

Reaktionsbedingungen

Temperatur60 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05622952
Quelldatensatzuspto-grants-1997_04
ORD IDord-19403b3bc7c64946ad61d19ad5730eac
Quellennotizuspto-grants-1997_04