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HRID 229685생성일: 2026년 10월 24일

Ammonia → 3-(1-Adamantyl)-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-one

https://huagongshe.com/ko/reaction/229685

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물3-Bromo-1-phenyl-5-(pyridin-2-yl)-1,2-dihydropyridin-2-oneHCID 22319065—
반응물HCID 178419756HCID 178419756—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178477754HCID 178477754—
용매TetrahydrofuranHCID 8028—
생성물3-(1-Adamantyl)-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-oneHCID 22319245—

반응 단계

40 mg of 3-bromo-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-one was dissolved in 10 ml of tetrahydrofuran. To the mixture were added 5 mg of [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium (II) and 1.2 mg of copper (I) iodide. While stirring the mixture at room temperature in nitrogen atmosphere overnight, 0.4 ml of 1-adamantyl zinc bromide (0.5M tetrahydrofuran solution) was added dropwise thereinto. After stirring in nitrogen atmosphere overnight, an aqueous ammonia was added thereto, 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 번호US07563811B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-fb7248b1c00c4b6f9ac0e0edad1c6ba7
출처 메모uspto-grants-2009_07