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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1650722생성일: 2026년 10월 24일

Isopropylamine → Ethyl-5-phenyl-4-(2-pyridinyl)-1H-pyrazole-1-acetate

https://huagongshe.com/ko/reaction/1650722

반응식

참여 물질

역할이름HCID투입량
반응물IsopropylamineHCID 6363—
반응물1-Phenyl-2-(2-pyridinyl)ethanoneHCID 74179—
반응물Dimethylformamide dimethyl acetalHCID 78373—
반응물Acetic acid, 2-hydrazinyl-, ethyl ester, hydrochloride (1:1)HCID 11593468—
용매EthanolHCID 702—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
용매tert-Butyl methyl etherHCID 15413—
생성물Ethyl-5-phenyl-4-(2-pyridinyl)-1H-pyrazole-1-acetateHCID 1508605061.6%

반응 단계

A solution of 26 g (0.132 mol) of 1-phenyl-2-(2-pyridinyl)ethanone and 19.3 mL (0.145 mol) of dimethylformamide dimethylacetal in 100 mL of methyl t-butyl ether was refluxed 4 hr. Because TLC on silica gel with 10% isopropylamine in ethyl acetate showed little reaction, another 20 mL of DMF dimethylacetal was added and the solution refluxed a further 6 hr. The solvent was stripped and the resulting crude, oily β-ketoenamine was dissolved in 400 mL of ethanol. The ethanol solution was heated to 40° with 22 g (0.143 mol) of ethyl hydrazinoacetate hydrochloride for about 1.5 hr. The solvent was stripped, and the resulting impure product was dissolved in a small amount of methylene dichloride and applied to a column of 850 g of silica gel. The column was eluted with 2:1 hexane-ethyl acetate to yield 25 g of yellow solid product, mp 98°-100° C. after evaporation of the solvent.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04925857
출처 데이터셋uspto-grants-1990_05
ORD IDord-60b73e2681bd476d9b806b0a330e7602
출처 메모uspto-grants-1990_05