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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1410512Erstellt: 25. Oktober 2026

Methanol → 5-(4-Aminophenylamino)-2-(2,6-difluorophenyl)oxazole-4-carbonitrile

https://huagongshe.com/reaction/1410512

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt2-(2,6-Difluorophenyl)-5-(4-nitrophenylamino)oxazole-4-carbonitrileHCID 59587430—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-(4-Aminophenylamino)-2-(2,6-difluorophenyl)oxazole-4-carbonitrileHCID 5958745090,7%

Reaktionsschritte

A solution of 2-(2,6-difluorophenyl)-5-(4-nitrophenylamino)oxazole-4-carbonitrile (0.435 g, 1.271 mmol) in 50:50 MeOH:EtOAc (10 ml) was hydrogenated using a 10% Pd/C catalyst at 30° C. at atmospheric pressure using the Thales H-Cube at a flow rate of 1 ml/min. The organic layer was then reduced in vacuo to yield 5-(4-aminophenylamino)-2-(2,6-difluorophenyl)oxazole-4-carbonitrile (0.360 g, 1.153 mmol, 90%). 1H NMR (CD3OD) δ 6.74 (2H, d), 7.10 (2H, d), 7.14 (2H, t), 7.55 (1H, m). LCMS (2) Rt: 2.47 min; m/z (ES+) 313.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08921544B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-addb725541914a6894d19c9c3968827b
Quellennotizuspto-grants-2014_12