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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1366269Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1366269

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
PatentnummerUS07893074B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-0a38286668a24c23a8428189c674cb6b
Quellennotizuspto-grants-2011_02