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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 466010생성일: 2026년 10월 25일

Ethyl chloroformate → 3-(3-Methylpyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/466010

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물3-MethylpyridazineHCID 74208—
반응물2-Phenylpyrazolo[1,5-a]pyridineHCID 15620342—
용매DichloromethaneHCID 6344—
생성물3-(3-Methylpyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridineHCID 1515810832%

반응 단계

To a mixture of 2-phenylpyrazolo[1,5-a]pyridine (5.00 g), 3-methylpyridazine (2.90 g) and methylene chloride (20 ml), was added a solution of ethyl chloroformate (5.57 g) in methylene chloride for 17 minutes under ice-cooling and stirred for an hour at the same temperature and then for 6 hours and 40 minutes at room temperature. To the reaction mixture was added methylene chloride (20 ml), and washed with a solution of potassium carbonate (10 ml) and a saturated aqueous solution of sodium chloride (10 ml) and dried over magnesium sulfate. The solvent was removed and chromatographed on silica gel (70 g) with a mixture of n-hexane and ethyl acetate (2:1). The fractions containing the object compound were combined and evaporated in vacuo and recrystallized from a mixture of ethyl acetate and n-hexane to give 3-(3-methylpyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (2.36 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05155114
출처 데이터셋uspto-grants-1992_10
ORD IDord-729fa189f5d6439ca7a86dbb1b294f72
출처 메모uspto-grants-1992_10