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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1082262Erstellt: 26. Oktober 2026

Potassium Carbonate → 4-tert-butyl-N-[5-(3-methoxyphenoxy)-6-{2-(2-pyrimidinylamino)ethoxy}-pyrimidin-4-yl]benzenesulfonamide hydrate

https://huagongshe.com/reaction/1082262

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktDimethylacetamideHCID 31374—
Edukt2-ChloropyrimidineHCID 74404—
EduktN-{6-(2-aminoethoxy)-5-(3-methoxyphenoxy)pyrimidin-4-yl}-4-tert-butylbenzenesulfonamide hydrochlorideHCID 67654095—
LösungsmittelAmmonium ChlorideHCID 25517—
Produkt4-tert-butyl-N-[5-(3-methoxyphenoxy)-6-{2-(2-pyrimidinylamino)ethoxy}-pyrimidin-4-yl]benzenesulfonamide hydrateHCID 19689482161,1%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of Compound A (150 mg), 2-chloropyrimidine (61 mg), potassium carbonate (122 mg) and dimethylacetamide (1.5 ml) is heated with stirring at 100° C. for three days. The reaction solution is diluted with aqueous ammonium chloride solution, and extracted with ethyl acetate. The extract is washed and dried. The solvent is evaporated to remove the solvent, and the residue is purified by silica gel column chromatography (solvent; chloroform/methanol =100:1) and further recrystallized from ethyl acetate/n-hexane to give 4-tert-butyl-N-[5-(3-methoxyphenoxy)-6-{2-(2-pyrimidinylamino)ethoxy}-pyrimidin-4-yl]benzenesulfonamide hydrate (135 mg) as crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05589478
Quelldatensatzuspto-grants-1996_12
ORD IDord-bdcd16175ec840488b5a139991da87b5
Quellennotizuspto-grants-1996_12