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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 583112생성일: 2026년 10월 26일

1-Propanol → 4-Chloro-5-[3-{3-(4-formylpiperazin-1-yl)-propoxy}-4-methoxybenzylamino]-3(2H)-pyridazinone

https://huagongshe.com/reaction/583112

반응식

참여 물질

역할이름HCID투입량
반응물1-PropanolHCID 1031—
반응물TriethylamineHCID 8471—
반응물4,5-Dichloro-3-hydroxypyridazineHCID 73247—
반응물3-(3-(4-Formylpiperazin-1-yl)-propoxy]-4-methoxybenzylamineHCID 19689424—
용매WaterHCID 962—
생성물4-Chloro-5-[3-{3-(4-formylpiperazin-1-yl)-propoxy}-4-methoxybenzylamino]-3(2H)-pyridazinoneHCID 1585918847%

반응 단계

A mixture comprising 11.58 g of 3-[3-(4-formylpiperazin-1-yl)-propoxy]-4-methoxybenzylamine, 5.0 g of 4,5-dichloro-3(2H)-pyridazinone, 4.6 g of triethylamine, 50 ml of n-propanol and 50 ml of water, was refluxed under heating with stirring for 14 hours. The solvent was distilled off under reduced pressure, and an aqueous potassium carbonate solution was added to the obtained residue, and the mixture was extracted with chloroform. The organic layer was washed with water and a saturated sodium chloride aqueous solution and then dried over anhydrous sodium sulfate. Then, the solvent was distilled off, and the residue was purified by silica gel column chromatography to obtain 6.21 g of the above-identified compound as slightly yellow white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05929074
출처 데이터셋uspto-grants-1999_07
ORD IDord-8659d09b1e8e48e6a06d73e5bce93b23
출처 메모uspto-grants-1999_07