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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1655067Erstellt: 26. Oktober 2026

Nitrogen → 3-Fluoropyridine-2-sulfonamide

https://huagongshe.com/reaction/1655067

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktSodium ChlorideHCID 5234—
EduktHydrofluoric AcidHCID 14917—
EduktSodium BicarbonateHCID 516892—
Edukt3-Aminopyridine-2-sulfonamideHCID 14943702—
EduktSodium NitriteHCID 23668193—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt3-Fluoropyridine-2-sulfonamideHCID 1995793070%

Reaktionsschritte

5.3 g (0.030 mol) of 3-aminopyridin-2-ylsulfonamide are dissolved in 12 ml of dimethyl sulfoxide, and the solution is added dropwise at 0° C. to 14.3 g (0.72 mol) of hydrogen fluoride (exothermal reaction). 2.4 g (0.035 mol) of sodium nitrite are then added in portions at 0° C. After one hour, the mixture is heated to 70° C. (evolution of N2). After the reaction mixture has cooled, it is added to an ice/water mixture, sodium bicarbonate and sodium chloride are added, and the mixture is then extracted with tetrahydrofuran and ethyl acetate. The combined extracts are washed with a saturated sodium chloride solution, dried with magnesium sulfate, filtered and evaporated. The residue is stirred in diethyl ether/petroleum ether. Filtration gives 3.7 g of 3-fluoropyridin-2-ylsulfonamide (Compound No. 3.001) of a melting point of +124° to +125° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05410063
Quelldatensatzuspto-grants-1995_04
ORD IDord-429577d82d2a4a40b7f728b09be5c3bf
Quellennotizuspto-grants-1995_04