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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7772Erstellt: 24. Oktober 2026

2-Amino-4-chlorophenol → 5-Chloro-2-(3-methoxy-4-pyridin-2-ylphenyl)-1,3-benzoxazole

https://huagongshe.com/de/reaction/7772

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-4-chlorophenolHCID 7265—
Edukt3-Methoxy-4-(pyridin-2-yl)benzoic acidHCID 21956515—
LösungsmittelWaterHCID 962—
Produkt5-Chloro-2-(3-methoxy-4-pyridin-2-ylphenyl)-1,3-benzoxazoleHCID 10286672—

Reaktionsschritte

3-Methoxy-4-pyridin-2-yl benzoic acid (500 mg, 2.2 mmol), 2-amino-4-chlorophenol (620 mg, 4.3 mmol) and trimethyl silylpolyphosphate (2 mL) was heated to 180° C. overnight under argon. To the cooled reaction mixture, water (100 mL) was added and extracted with EtOAc (4×20 mL). Set aside organic layer. Filtered aqueous layer through Celite pad and basified filtrate to pH 9 (solid NaHCO3). Extracted with EtOAc (2×30 mL), combined all organic layers and concentrated in vacuo. The resulting orange oil was purified by flash chromatography using a gradient elution of 15:85 ethyl acetate:hexane to 1:1 ethyl acetate:hexane to give the desired intermediate, 5-chloro-2-(3-methoxy-4-pyridin-2-ylphenyl)-1,3-benzoxazole as a colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087601B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-14747b92927c4a008bd0c9dd2379904e
Quellennotizuspto-grants-2006_08