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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1624693생성일: 2026년 10월 26일

Ethylacetate methanol → Methyl 1-(4-bromo-2,5-difluorophenyl)-5-methoxy-4-oxo-1,4-dihydropyridazine-3-carboxylate

https://huagongshe.com/reaction/1624693

반응식

참여 물질

역할이름HCID투입량
반응물Ethylacetate methanolHCID 21584119—
반응물methyl 2-[(4-bromo-2,5-difluorophenyl)hydrazinylidene]-4-methoxy-3-oxobutanoateHCID 178496284—
용매Dimethylformamide dimethyl acetalHCID 78373—
생성물Methyl 1-(4-bromo-2,5-difluorophenyl)-5-methoxy-4-oxo-1,4-dihydropyridazine-3-carboxylateHCID 5807221383%

반응 단계

A solution of methyl 2-[(4-bromo-2,5-difluorophenyl)hydrazono]-4-methoxy-3-oxobutanoate (33 g, 90 mmol) in N,N-dimethylformamide dimethyl acetal (72 mL) was stirred at 110° C. for 3 h. After cooling to room temperature, the mixture was concentrated under reduce pressure. To the residue were added MeOH and silica gel The mixture was evaporated and purified by silica gel column chromatography eluting with hexane/AcOEt (1/0 to 0/1) and then AcOEt/MeOH (4/1) to give the title compound (27.9 g, 83% yield) as a brown gum: 1H NMR (300 MHz, DMSO-d5): δ ppm 3.80 (3H, s), 3.83 (3H, s), 8.01 (1H, dd, J=8.7, 6.8 Hz), 8.15 (1H, dd, J=9.8, 6.0 Hz), 8.55 (1H, d, J=1.5 Hz). LC-MS (ESI) m/z 376 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08778944B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-8fdc7721c46844c3a08ae79b4a2d6d8d
출처 메모uspto-grants-2014_07