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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10249Erstellt: 24. Oktober 2026

Allyl Alcohol → 4-i-Propyl-phenyl sulfamic acid-[6-allyloxy-5-(o-methoxyphenoxy)-2-(4-pyridyl)pyrimidin-4-yl]-amide

https://huagongshe.com/de/reaction/10249

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl AlcoholHCID 7858—
EduktTetrahydrofuranHCID 8028—
EduktSodium hydrideHCID 24758—
Edukt4-i-Propyl-phenyl sulfamic acid-[6-chloro-5-(o-methoxy-phenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-amideHCID 10279868—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-i-Propyl-phenyl sulfamic acid-[6-allyloxy-5-(o-methoxyphenoxy)-2-(4-pyridyl)pyrimidin-4-yl]-amideHCID 21979588—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a mixture of allyl alcohol (1 ml) and THF (2 ml) was added sodium hydride (100 mg, 60% dispersion in mineral oil) followed by the addition of 4-i-propyl-phenyl sulfamic acid-[6-chloro-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide (100 mg, Referential Example 1e)). DMF (0.5 ml) was added and the reaction mixture was heated to 80° C. for 20 h. The solvents were evaporated, water (14 ml) and a 10% solution of citric acid was added until the pH was 3. The precipitate was filtered off and washed with water and purified by chromatography through silicagel with EtOAc/Hex=3:2 to give 4-i-propyl-phenyl sulfamic acid-[6-allyloxy-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide (10 mg). tR=5.36 min, (LC); [M+H]+=548.46 (ES+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094781B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-a308b8d7315b46f3a3735372c111dddd
Quellennotizuspto-grants-2006_08