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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 547726생성일: 2026년 10월 23일

1-Phenyl-1,4-pentanedione → 3-(2-Methyl-5-phenylpyrrol-1-yl)-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-one

https://huagongshe.com/ko/reaction/547726

반응식

참여 물질

역할이름HCID투입량
반응물1-Phenyl-1,4-pentanedioneHCID 136371—
반응물Sodium BicarbonateHCID 516892—
반응물3-Amino-1-phenyl-5-(2-pyridyl)-1,2-dihydropyridin-2-oneHCID 22319119—
촉매p-Toluenesulfonic acidHCID 6101—
용매TolueneHCID 1140—
생성물3-(2-Methyl-5-phenylpyrrol-1-yl)-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-oneHCID 2231923531.3%

반응 단계

25 mg of 3-amino-1-phenyl-5-(2-pyridyl)-1,2-dihydropyridin-2-one was dissolved in 10 ml of toluene. To the mixture were added 20 mg of 1-phenyl-1,4-pentandione and 0.2 mg of p-toluenesulfonate (hydrate), followed by heating under reflux for 1 hour. After cooling to room temperature, the reaction mixture was poured into a saturated aqueous solution of sodium hydrogen carbonate, followed by extracting with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel chromatography (hexane/ethyl acetate system), to give 12 mg of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07939549B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-783f50cec41745ea97a69fd5a54bdf6e
출처 메모uspto-grants-2011_05