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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 703957생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/703957

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 번호US04985444
출처 데이터셋uspto-grants-1991_01
ORD IDord-15d3dca0671446f8bf98df65312ce056
출처 메모uspto-grants-1991_01