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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 424180Erstellt: 25. Oktober 2026

Pyridine → 2-Amino-5-[(methylsulfonyl)amino]benzenesulfonamide

https://huagongshe.com/reaction/424180

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt2,5-Diamino-benzenesulfonamide methanesulfonateHCID 25164641—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-Amino-5-[(methylsulfonyl)amino]benzenesulfonamideHCID 2495065786,3%

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

2,5-Diamino-benzenesulfonamide methanesulfonate (1.80 kg, 6.35 mol) was suspended in acetonitrile (24 L). Pyridine (1.55 L, 19.1 mol) was added, followed by the careful slow addition of methanesulfonyl chloride (517 mL, 6.68 mol). After stirring at 23° C. for 20 h, the mixture was partially concentrated in vacuo at 55° C. Water (18 L) was added to the concentrate, and the resulting suspension was stirred at 23° C. for 2 h. The solid was filtered and was then washed with water (4 L) and air dried on the filter. The solid was suspended in absolute ethanol (9 L), stirred at 23° C. for 9 h, and was then filtered. The solid was washed with absolute ethanol (2×2 L), and was then further dried in vacuo at 50° C. to afford the desired product, 2-amino-5-methanesulfonylamino-benzenesulfonamide (1.45 kg, 5.48 mol, 86%), as a purple solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08101800B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-e211364c44764adc8de3a06420094d63
Quellennotizuspto-grants-2012_01