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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2266Erstellt: 23. Oktober 2026

Piconol → 4-tert-butyl-N-{5-(3-methoxyphenoxy)-6-(2-pyridinylmethoxy)pyrimidin-4-yl}benzenesulfonamide

https://huagongshe.com/de/reaction/2266

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiconolHCID 11474—
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
Eduktp-t-butyl-N-[6-chloro-5-(m-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamideHCID 15391273—
LösungsmittelDimethylacetamideHCID 31374—
Produkt4-tert-butyl-N-{5-(3-methoxyphenoxy)-6-(2-pyridinylmethoxy)pyrimidin-4-yl}benzenesulfonamideHCID 1539127194,6%

Reaktionsschritte

To a stirred solution of pyridine-2-methanol (130 mg) in dimethylacetamide (0.5 ml) is added gradually with stirring sodium hydride (62.7% dispersion-type, 60 mg) under ice-cooling, and thereto is added 4-tert-butyl-N-{6-chloro-5-(3-methoxyphenoxy)pyrimidin-4-yl}benzenesulfonamide (100 mg). The mixture is reacted at 100° C. for 30 minutes, and cooled. The pH value of the mixture is adjusted to pH 8 with saturated aqueous ammonium chloride solution. The mixture is extracted with ethyl acetate, and the extract is washed, dried, and concentrated to dryness under reduced pressure. The residue is crystallized from ethyl acetate to give 4-tert-butyl-N-{5-(3-methoxyphenoxy)-6-(2-pyridinylmethoxy)pyrimidin-4-yl}benzenesulfonamide (110 mg) as crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728706
Quelldatensatzuspto-grants-1998_03
ORD IDord-68b5d1780faa448bb947e87b6999fd2f
Quellennotizuspto-grants-1998_03