Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2424372Erstellt: 26. Oktober 2026

2-Aminobenzenesulfonamide → 2-(5-Bromo-2-chloropyrimidin-4-ylamino)benzenesulfonamide

https://huagongshe.com/reaction/2424372

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminobenzenesulfonamideHCID 72894—
Edukt5-Bromo-2,4-dichloropyrimidineHCID 289973—
EduktSodium BicarbonateHCID 516892—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelIsopropanolHCID 3776—
Produkt2-(5-Bromo-2-chloropyrimidin-4-ylamino)benzenesulfonamideHCID 85997992—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a solution of 5-bromo-2,4-dichloropyrimidine (300 mg, 1.32 mmol) and 2-amino-benzenesulfonamide (340 mg, 1.97 mmol) in 2-propanol (3 mL), concentrated hydrochloric acid (0.06 mL) is added and the mixture is stirred at 90° C. for 4.5 hours. The mixture is poured into aqueous sodium hydrogen carbonate and extracted with ethyl acetate three times. The organic layer is washed with water, dried over sodium sulfate, and evaporated in vacuo. The residue is purified by column chromatography (hexane:ethyl acetate=2:1) to afford the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07964592B2
Quelldatensatzuspto-grants-2011_06
ORD IDord-9ba9abeff4444547803d41d037ddf6a7
Quellennotizuspto-grants-2011_06