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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7772생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-4-chlorophenolHCID 7265—
반응물3-Methoxy-4-(pyridin-2-yl)benzoic acidHCID 21956515—
용매WaterHCID 962—
생성물5-Chloro-2-(3-methoxy-4-pyridin-2-ylphenyl)-1,3-benzoxazoleHCID 10286672—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-14747b92927c4a008bd0c9dd2379904e
출처 메모uspto-grants-2006_08