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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 218194Erstellt: 26. Oktober 2026

Cesium carbonate → 4-tert-butyl-N-[5-chloro-2-(4-nitro-pyrazol-1-yl)-pyridin-3-yl]-benzenesulfonamide

https://huagongshe.com/reaction/218194

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt4-nitro-1H-pyrazoleHCID 16376—
Edukttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
EduktN-(2-bromo-5-chloro-pyridin-3-yl)-4-tert-butyl-benzenesulfonamideHCID 57942597—
KatalysatorCopper iodideHCID 83717—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelDimethylacetamideHCID 31374—
Produkt4-tert-butyl-N-[5-chloro-2-(4-nitro-pyrazol-1-yl)-pyridin-3-yl]-benzenesulfonamideHCID 68464085—

Reaktionsschritte

A solution of N-(2-bromo-5-chloro-pyridin-3-yl)-4-tert-butyl-benzene sulfonamide (534 mg, 1.32 mmol), 4-nitropyrazole (224 mg, 1.98 mmol), trans-N,N′-dimethyl-cyclohexane-1,2-diamine (42 μL, 0.264 mmol), copper iodide (51 mg, 0.264 mmol), and cesium carbonate (903 mg, 2.77 mmol) in 5 mL of N,N-dimethylacetamide was heated at 130° C. for 2 hours. Ethyl acetate and water were added and the layers were separated. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude reside was subsequently purified by flash column chromatography (0-100% ethyl acetate in hexanes) to afford 4-tert-butyl-N-[5-chloro-2-(4-nitro-pyrazol-1-yl)-pyridin-3-yl]-benzenesulfonamide as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08198309B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-c121f3fbfb78455b8f965e07474b56bd
Quellennotizuspto-grants-2012_06