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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454940생성일: 2026년 10월 24일

Triethylamine → 1-(1-(3,6-Dichloropyridazin-4-yl)piperidin-4-yl)ethanone

https://huagongshe.com/ko/reaction/454940

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3,4,6-TrichloropyridazineHCID 95123—
반응물1-(Piperidin-4-yl)ethan-1-oneHCID 2723764—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-(1-(3,6-Dichloropyridazin-4-yl)piperidin-4-yl)ethanoneHCID 5854795739%

반응 단계

Triethylamine (2.2 g, 20.0 mmol), 3,4,6-trichloro-pyridazine (1.8 g, 10.0 mmol) and 1-(piperidin-4-yl)ethanone (1.3 g, 10.0 mmol) was dissolved in DMF (20 mL) and the resulting mixture was stirred at room temperature overnight. The mixture was then diluted with water (50 mL) and extracted with EtOAc (2×50 mL). The combined organic extracts were combined and washed with water (20 mL) and brine (20 mL), dried over Na2SO4, and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography on silica gel (20% to 50% EtOAc in hexanes) to give 1-(1-(3,6-dichloropyridazin-4-yl)piperidin-4-yl)ethanone (1.0 g, 3.8 mmol, 39% yield) as white solid. ESI-MS (M+1): 274 calc. for C11H13ClN3O 273.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497265B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-9f93ca938d46472888460804cf7f0d07
출처 메모uspto-grants-2013_07