돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1662020생성일: 2026년 10월 24일

Pyridine → Ethyl 4,6-dimethyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/ko/reaction/1662020

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Phenylboronic AcidHCID 66827—
반응물Ethyl 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 247443—
용매1,4-DioxaneHCID 31275—
생성물Ethyl 4,6-dimethyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxylateHCID 1383792531.2%

반응 조건

온도80 °C

반응 단계

A suspension of ethyl 4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carboxylate (7.5 g, 0.038 mol), phenylboronic acid (14.1 g, 0.115 mol), cupric acetate (1.38 g, 0.008 mol), pyridine (7.5 mL) in 1,4-dioxane (80 mL) is heated at 80° C. for 96 hours. The solid is filtered off and the filtrate is concentrated. The residue is partitioned with EtOAc (50 mL) and 2N HCl (70 mL), and the precipitate is collected by filtration and washed with EtOAc to give the title product (2.95 g). The EtOAc solution is separated, dried and concentrated. The residue is purified by silica gel column chromatography eluting with PE:acetone (2:1) to give another portion of (0.3 g). (3.25 g, 31.2% yield). MS (m/z): 272.0 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08030302B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-57e49fb0763f41c6a6b13c00bfa96d11
출처 메모uspto-grants-2011_10