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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1619603Erstellt: 27. Oktober 2026

Hydrochloric Acid → 3-Cyano-N-(5-fluoropyridin-2-yl)-4-{[3-(1-methyl-1H-pyrazol-5-yl)biphenyl-4-yl]oxy}benzenesulfonamide

https://huagongshe.com/reaction/1619603

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium CarbonateHCID 11430—
Edukt3-cyano-4-fluoro-N-(5-fluoropyridin-2-yl)benzenesulfonamideHCID 59436600—
Edukt3-(1-methyl-1H-pyrazol-5-yl)biphenyl-4-olHCID 136200891—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt3-Cyano-N-(5-fluoropyridin-2-yl)-4-{[3-(1-methyl-1H-pyrazol-5-yl)biphenyl-4-yl]oxy}benzenesulfonamideHCID 5660118818%

Reaktionsschritte

In a pressure sealed vial, 3-(1-methyl-1H-pyrazol-5-yl)biphenyl-4-ol (Preparation 107, mg, 0.19 mmol), 3-cyano-4-fluoro-N-(5-fluoropyridin-2-yl)benzenesulfonamide (WO2010079443, 50 mg, 0.17 mmol) and potassium carbonate (70 mg, 0.51 mmol) were stirred at 90° C. in dimethyl sulfoxide for 18 hours. The mixture was cooled down to room temperature and treated with 2M hydrochloric acid (5 mL). The mixture was stirred for 1 hour and the resulting precipitate was filtered and purified by preparative HPLC to afford the title compound (17 mg, 18%) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08772293B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-b11b70dbe51f41ae965e70c0258030aa
Quellennotizuspto-grants-2014_07