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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13333Erstellt: 23. Oktober 2026

p-Toluenesulfonic acid → HCID 23145188, Verbindung

https://huagongshe.com/de/reaction/13333

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
EduktPotassium CarbonateHCID 11430—
EduktStannous chloride dihydrateHCID 61436—
Edukt2,6-DifluorophenolHCID 94392—
EduktN-(2,3-difluoro-4-(6-methanesulfonyl-pyridin-3-yloxy)-6-nitro-phenyl)pyrazinecarboxamideHCID 23145537—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktHCID 23145188HCID 23145188—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

8 mg of 2,6-difluorophenol and 8 mg of potassium carbonate were added to an N-methylpyrrolidinone (0.5 ml) solution of 8.6 mg of N-(2,3-difluoro-4-(6-methanesulfonyl-pyridin-3-yloxy)-6-nitro-phenyl)pyrazinecarboxamide, and the reaction liquid was stirred at 90° C. for 15 minutes. 75 mg of tin(II) chloride dihydrate was added to it, and the reaction liquid was stirred overnight at 90° C. Further, 3 mg of p-toluenesulfonic acid was added to it, and the reaction liquid was stirred at 90° C. for 2 hours. The deposit was taken out through filtration, and purified through reversed-phase middle-pressure liquid chromatography [ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid]. The solvent of the resulting fraction was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain the entitled compound as a brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728025B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-c87dc0f010dc41a69867e6328807e9df
Quellennotizuspto-grants-2010_06