Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1913613Erstellt: 23. Oktober 2026

Tetrahydrofuran → 2-(3-Bromopyridin-4-yl)-5-(trifluoromethyl)benzoxazole

https://huagongshe.com/de/reaction/1913613

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktTriphenylphosphineHCID 11776—
Eduktethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Edukt3-bromo-N-[2-hydroxy-5-(trifluoromethyl)phenyl]isonicotinamideHCID 66879880—
LösungsmittelTolueneHCID 1140—
Produkt2-(3-Bromopyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 6688091787,1%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a mixture of 0.29 g of 3-bromo-N-[2-hydroxy-5-(trifluoromethyl)phenyl]isonicotinamide, 4 ml of tetrahydrofuran and 0.25 g of triphenylphosphine, 0.42 g of 40% toluene solution of diethyl azodicarboxylate was added dropwise at room temperature. The reaction mixture was stirred while heating at 50° C. for 1.5 hours. The reaction mixture was cooled to room temperature, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.24 g of 2-(3-bromopyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 27”).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08609705B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-5086dda980724981977988f9deade821
Quellennotizuspto-grants-2013_12