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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 478314생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/478314

반응식

참여 물질

역할이름HCID투입량
반응물3-Bromo-4-fluorobenzaldehydeHCID 173604—
반응물2H-pyran-3,5(4H,6H)-dioneHCID 325287—
반응물ethyl (2E)-3-amino-2-hexenoateHCID 10986503—
용매EthanolHCID 702—
생성물ethyl 4-(3-bromo-4-fluorophenyl)-5-oxo-2-propyl-4,5,6,8-tetrahydro-1H-pyrano[3,4-b]pyridine-3-carboxylateHCID 1800099788.2%

반응 단계

The product from Example 95A (0.083 g, 0.52 mmol), the product from Example 11B (0.050 g, 0.44 mmol) and 3-bromo-4-fluorobenzaldehyde (0.116 g, 0.57 mmol) in ethanol (1 mL) were heated to 80 C. for 16 hours in a sealed tube, cooled to ambient temperature and concentrated to dryness. The residue was purified on silica gel eluting with 2% methanol in dichloromethane to provide the title compound (0.17 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06642222B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-53a2bef521b4435aa8bc35dcf5e41010
출처 메모uspto-grants-2003_11