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HRID 7772作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4-chlorophenolHCID 7265—
反応物3-Methoxy-4-(pyridin-2-yl)benzoic acidHCID 21956515—
溶媒WaterHCID 962—
生成物5-Chloro-2-(3-methoxy-4-pyridin-2-ylphenyl)-1,3-benzoxazoleHCID 10286672—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087601B2
出典データセットuspto-grants-2006_08
ORD IDord-14747b92927c4a008bd0c9dd2379904e
出典メモuspto-grants-2006_08