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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81359생성일: 2026년 10월 25일

2-Fluorophenol → 5-(2-Fluoro-phenoxy)-2-(4-methoxy-3,5-dimethyl-phenyl)-oxazolo[5,4-d]pyrimidine

https://huagongshe.com/reaction/81359

반응식

참여 물질

역할이름HCID투입량
반응물2-FluorophenolHCID 9707—
반응물Sodium hydrideHCID 24758—
반응물5-Chloro-2-(4-methoxy-3,5-dimethylphenyl)oxazolo[5,4-d]pyrimidineHCID 86675954—
용매DimethylacetamideHCID 31374—
생성물5-(2-Fluoro-phenoxy)-2-(4-methoxy-3,5-dimethyl-phenyl)-oxazolo[5,4-d]pyrimidineHCID 53311373—

반응 단계

149 mg of sodium hydride were added under an argon atmosphere to a solution of 418 mg of 2-fluoro-phenol in 15 ml dimethylacetamide. After stirring for 30 min at room temperature a solution of 900 mg of 5-chloro-2-(4-methoxy-3,5-dimethyl-phenyl)-oxazolo[5,4-d]pyrimidine in 20 ml dimethylacetamide was added slowly. The mixture was allowed to stir for 1.5 h at room temperature. Upon consumption of the starting oxazolo[5,4-d]pyrimidine an aqueous solution of citric acid (100 g/l) was added until the pH was neutral. The aqueous layer was extracted twice with 15 ml of ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered and the solvents were removed in vacuo. The title compound was isolated by silica gel chromatography (heptane/ethyl acetate gradient) as a white solid. Yield: 820 mg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846690B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b0a87601989c458e9eb5b0a7ac85ad9f
출처 메모uspto-grants-2014_09