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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2195535생성일: 2026년 10월 26일

Pyridine → Ethyl 1-(4-fluorophenyl)-4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/2195535

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Ethyl 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 247443—
반응물4-Fluorophenylboronic acidHCID 285645—
용매1,4-DioxaneHCID 31275—
생성물Ethyl 1-(4-fluorophenyl)-4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 6676711916.6%

반응 조건

온도80 °C

반응 단계

A suspension of ethyl 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylate (5.0 g, 0.025 mol), 4-fluorophenylboronic acid (10.7 g, 0.077 mol), cupric acetate (1.33 g, 0.007 mol), pyridine (6.86 mL), and 4 A molecular sieves (5.0 g) in 1,4-dioxane (80 mL) is heated at 80° C. for 68 hours. The solids are filtered off and the filtrate is concentrated. The residue is partitioned with EtOAc (50 mL) and 2N HCl (70 mL). The precipitated solid is collected by filtration and washed with EtOAc to give the title product (1.2 g). The EtOAc filtrate is separated, dried and concentrated. The residue is purified by silica gel column chromatography eluting with PE:EtOAc:MeOH (40:20:1) to give another portion of product (0.12 g), (1.32 g total, 17.8% yield). MS (m/z): 290.1 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE043878E1
출처 데이터셋uspto-grants-2012_12
ORD IDord-2eece15bb868492e885db24154f98c9c
출처 메모uspto-grants-2012_12