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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 723899생성일: 2026년 10월 25일

ethyl (2R)-oxirane-2-carboxylate → 3-[3-fluoro-4-(4-oxo-3,4-dihydro-2H-pyridin-1-yl)phenylamino]-2(R)-hydroxypropionic acid ethyl ester

https://huagongshe.com/reaction/723899

반응식

참여 물질

역할이름HCID투입량
반응물ethyl (2R)-oxirane-2-carboxylateHCID 1512667—
반응물Trifluoromethanesulfonic acid, lithium saltHCID 3664839—
반응물1-(4-Amino-2-fluoro-phenyl)-2,3-dihydro-1H-pyridin-4-oneHCID 21877877—
용매AcetonitrileHCID 6342—
생성물3-[3-fluoro-4-(4-oxo-3,4-dihydro-2H-pyridin-1-yl)phenylamino]-2(R)-hydroxypropionic acid ethyl esterHCID 6848710245%

반응 단계

A solution of 1-(4-amino-2-fluorophenyl)-2,3-dihydro-1H-pyridin-4-one (Step 4, 0.412 g, 2.0 mmol) and oxirane-2(R)-carboxylic acid ethyl ester (0.394 g, 3.4 mmol) with lithium triflate (0.360 g, 3.0 mmol) in dry acetonitrile (5.0 mL) is heated at 50–60° C. for 24 h. Volatiles are removed under vacuum, and the crude material purified by silica gel flash chromatography (eluent: 5% acetone in CH2Cl2) to afford the title compound (290 mg, 45%) as a viscous yellow oil, MS (m/z): 323 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141588B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-968a0eb5cda14a0bb282c1afaddf6c99
출처 메모uspto-grants-2006_11