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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1432712생성일: 2026년 10월 25일

Chloroacetone → 4-(1-Ethyl-propyl)-2-methoxy-6-methyl-pyrrolo[1,2-b]pyridazine

https://huagongshe.com/reaction/1432712

반응식

참여 물질

역할이름HCID투입량
반응물ChloroacetoneHCID 6571—
반응물Sodium BicarbonateHCID 516892—
반응물N-[4-(1-Ethyl-propyl)-6-methoxy-pyridazin-3-yl]-2,2-dimethyl-propionamideHCID 68840437—
촉매ZincchlorideHCID 3007855—
용매EthanolHCID 702—
생성물4-(1-Ethyl-propyl)-2-methoxy-6-methyl-pyrrolo[1,2-b]pyridazineHCID 6884195411%

반응 단계

A solution of N-[4-(1-ethyl-propyl)-6-methoxy-pyridazin-3-yl]-2,2-dimethyl-propionamide (5.32 g, 19.08 mmol) in EtOH (250 mL) is treated with ZnCl2 (26.0 g, 190.8 mmol) and refluxed for 48 h. The reaction is cooled to rt and concentrated. The residue is taken up with EtOAc (250 mL), and H2O (100 mL). It is washed with H2O (2×100 mL); dried with Na2SO4; filtered and concentrated. The residue is then dissolved in EtOAc (80 mL), reacted with chloroacetone (1.6 mL, 20.03 mmol.) at reflux overnight. While it is hot, NaHCO3 (8.10 g) is added and the reaction is refluxed for 1 h. It is cooled to rt and filtered through silica gel washed with EtOAc and concentrated. Purification of the crude material by chromatography gives the title compound (0.48 g, 2.07 mmol, 11%). 1H NMR (CDCl3): δ. 0.84 (t, J=7.5 Hz, 6H), 1.69-1.869 (m, 4H), 2.45 (s, 3H), 3.19-3.30 (m, 1H), 3.94 (s, 3H), 6.39 (s, 1H), 7.49 (s, 1H). ES-MS (m/z): calcd for C14H20N2O (M+H)+: 233.3; found: 234.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07612067B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-bb5c024b94f041ca9f0a334f734cb00f
출처 메모uspto-grants-2009_11