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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2303Erstellt: 24. Oktober 2026

2-{6-Azido-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol → 2-{6-Amino-5-(4-methylphenyl)-pyrimidin-4-yloxy}ethanol

https://huagongshe.com/de/reaction/2303

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-{6-Azido-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanolHCID 11807790—
KatalysatorHCID 178418390HCID 178418390—
LösungsmittelEthanolHCID 702—
Produkt2-{6-Amino-5-(4-methylphenyl)-pyrimidin-4-yloxy}ethanolHCID 1111829789,7%

Reaktionsschritte

A mixture of 2-{6-azido-5-(4-methylphenyl)pyrimidin-4-yloxy}-ethanol (19.6 g), 10% palladium-carbon (50% moist) (4.0 g) and ethanol (240 ml) is subjected to catalytic hydrogenation at room temperature under hydrogen atmosphere (1 atm) for one hour. The catalyst is removed by filtration, and the filtrate is concentrated under reduced pressure. The residue is recrystallized from ethyl acetate/n-hexane to give 2-{6-amino-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol (15.9 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728706
Quelldatensatzuspto-grants-1998_03
ORD IDord-5cec6056ae4c4169bd4252bc117b2be6
Quellennotizuspto-grants-1998_03