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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 478270생성일: 2026년 10월 24일

3-Bromo-4-fluorobenzaldehyde → methyl 4-(3-bromo-4-fluorophenyl)-2-methyl-5-oxo-4,5,6,8-tetrahydro-1H-pyrano[3,4-b]pyridine-3-carboxylate

https://huagongshe.com/ko/reaction/478270

반응식

참여 물질

역할이름HCID투입량
반응물3-Bromo-4-fluorobenzaldehydeHCID 173604—
반응물2H-pyran-3,5(4H,6H)-dioneHCID 325287—
반응물Methyl 3-aminocrotonateHCID 643918—
용매EthanolHCID 702—
생성물methyl 4-(3-bromo-4-fluorophenyl)-2-methyl-5-oxo-4,5,6,8-tetrahydro-1H-pyrano[3,4-b]pyridine-3-carboxylateHCID 1125796450.5%

반응 단계

A mixture of tetrahydropyran-3,5-dione (Terasawa, J. Org. Chem. (1977), 42, 1163-1169) (1.4 g, 12 mmol), 3-bromo-4-fluorobenzaldehyde (3.0 g, 15 mmol), methyl 3-aminocrotonate (1.4 g, 12 mmol) and ethyl alcohol (10 mL) was processed as described in Example 2A. Purification by flash chromatography over silica gel (1% then 2% and then 5% methyl alcohol/methylene chloride) provided the title compound (2.4 g) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06642222B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-6f069885456a488c9abd175de1e5d856
출처 메모uspto-grants-2003_11