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HRID 229692作成日:2026年10月25日

Water → 3-Cyclohexyl-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-one

https://huagongshe.com/reaction/229692

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-Bromo-1-phenyl-5-(pyridin-2-yl)-1,2-dihydropyridin-2-oneHCID 22319065—
反応物HCID 178478990HCID 178478990—
触媒Dichloro(1,1'-(1,3-propanediyl)bis(1,1-diphenylphosphine-kappaP))nickelHCID 2724937—
溶媒TetrahydrofuranHCID 8028—
生成物3-Cyclohexyl-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-oneHCID 22319216—

反応手順

34 mg of 3-bromo-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-one was dissolved in 10 ml of tetrahydrofuran, followed by adding 1 mg of [1,3-bis(diphenylphosphino)propane] nickel (II) chloride. Under stirring in nitrogen atmosphere, 0.1 ml of cyclohexyl magnesium chloride (2.0M ether solution) was added dropwise thereinto. The mixutre was stirred at room temperature in nitrogen atmosphere for 1 hour, followed by heating under reflux for 72 hours. After cooling to room temperature, water was added thereto, followed by extracting with ethyl acetate. The organic layer was washed with brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel chromatography (chloroform/methanol system), to give 5 mg of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07563811B2
出典データセットuspto-grants-2009_07
ORD IDord-01447dd4a0404ca7a45596b81717fa58
出典メモuspto-grants-2009_07