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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 469192생성일: 2026년 10월 25일

Methanesulfonic Acid → 6-(Difluoro(6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo(4,3-b)pyridazin-3-yl)methyl)quinoline

https://huagongshe.com/reaction/469192

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazineHCID 54595607—
반응물2,2-Difluoro-2-(quinolin-6-yl)acetohydrazideHCID 58955250—
용매1-Methoxy-2-propanolHCID 7900—
생성물6-(Difluoro(6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo(4,3-b)pyridazin-3-yl)methyl)quinolineHCID 46911863—

반응 조건

온도80 °C

반응 단계

To a reactor under inert atmosphere was added 73.84 g (0.38 mol) 3-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazine, 90 g (0.38 mol) 2,2-difluoro-2-quinolin-6-ylacetohydrazide and 1200 mL 1-methoxy-2-propanol. Then 29.85 mL (0.455 mol) methane sulphonic acid was added and the reaction mixture was heated at 80° C. for 8 hours. After cooling to ambient temperature the mesylate salt of the title compound was filtered off from the reaction mixture. This salt was dissolved in a mixture of 400 mL ethanol and 300 mL water, after alkalisation at 80° C. with 50 mL ammonia (0.65 mol) in 200 mL water the free base of the title compound precipitates and was filtered off. This precipitate was dried at 50° C. and was subsequently re-crystallized from 2-propanol (1.8 L/mol) to yield the title compound in 75% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629144B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-fab948e106634ced905aff24968ac977
출처 메모uspto-grants-2014_01