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HRID 465997생성일: 2026년 10월 25일

Pyridazine → 3-(1-Ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/465997

반응식

참여 물질

역할이름HCID투입량
반응물PyridazineHCID 9259—
반응물Ethyl chloroformateHCID 10928—
반응물2-Phenylpyrazolo[1,5-a]pyridineHCID 15620342—
용매DichloromethaneHCID 6344—
생성물3-(1-Ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridineHCID 1179186053.4%

반응 조건

온도10 °C

반응 단계

Ethyl chloroformate (3.38 g) was added dropwise with stirring to a solution of 2-phenylpyrazolo[1,5-a]pyridine (2.54 g) and pyridazine (5.00 g) in methylene chloride (5.0 ml) at 10° C. After being stirred at 10° C. for 1 hour and then at room temperature for 2 hours, the reaction mixture was poured onto ice-water (100 ml), and extracted with ethyl acetate. The combined extracts were washed with saturated sodium chloride aqueous solution (100 ml), dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel (150 g) with a mixture of chloroform and n-hexane (1:1) as an eluant. The fractions containing main-product [compound (A)] were combined and evaporated in vacuo to give 3-(1-ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (2.42 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05155114
출처 데이터셋uspto-grants-1992_10
ORD IDord-c7262b43437944ed8a03a8289694a8d5
출처 메모uspto-grants-1992_10