돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1673203생성일: 2026년 10월 25일

Tetrahydrofuran → 6-(4-Chlorophenyl)-7-(2,4-dichlorophenyl)-2-methyl-2,3-dihydro-4H-pyrano[2,3-b]pyridin-4-one

https://huagongshe.com/reaction/1673203

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물6-(2,4-Dichlorophenyl)-5-(4-chlorophenyl)-2-oxo-1,2-dihydropyridine-3-carbonitrileHCID 21984825—
반응물HCID 178418689HCID 178418689—
반응물HCID 178456053HCID 178456053—
생성물6-(4-Chlorophenyl)-7-(2,4-dichlorophenyl)-2-methyl-2,3-dihydro-4H-pyrano[2,3-b]pyridin-4-oneHCID 25060539—

반응 조건

온도50 °C

반응 단계

To the product of Example 1 Step B (7.0 g, 18.6 mmol in THF (90 mL) was added MeMgBr (1.4 M in toluene/THF, 14 mL, 19.6 mmol). After stirring for 3 min, prop-1-enylmagnesium bromide (0.5 M in THF, 55.9 mL, 28 mmol) was added and the temperature was increased to 50° C. The reaction was quenched with 2 M HCl after 30 min and diluted with EtOAc. The solution was washed with brine, and concentrated The residue was purified by flash chromatography on silica gel gradient eluted with 0-35% EtOAc in hexane to afford the title compound. (LC-2) HPLC/MS: 418.2 (M+1), 420.2 (M+3); Rt=4.08 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07999107B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-b796778ead8f430181fc6a2b07ccb44b
출처 메모uspto-grants-2011_08