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HRID 547726作成日:2026年10月24日

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/ja/reaction/547726

反応式

関与物質

役割名称HCID仕込み量
反応物1-Phenyl-1,4-pentanedioneHCID 136371—
反応物Sodium BicarbonateHCID 516892—
反応物3-Amino-1-phenyl-5-(2-pyridyl)-1,2-dihydropyridin-2-oneHCID 22319119—
触媒p-Toluenesulfonic acidHCID 6101—
溶媒TolueneHCID 1140—
生成物3-(2-Methyl-5-phenylpyrrol-1-yl)-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-oneHCID 2231923531.3%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07939549B2
出典データセットuspto-grants-2011_05
ORD IDord-783f50cec41745ea97a69fd5a54bdf6e
出典メモuspto-grants-2011_05