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HRID 28536생성일: 2026년 10월 23일

Sodium Carbonate → 4-Chloro-6-(2,5-dichloro-phenyl)-pyrimidin-2-yl-amine

https://huagongshe.com/ko/reaction/28536

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물TriphenylphosphineHCID 11776—
반응물2-Amino-4,6-dichloropyrimidineHCID 65522—
반응물2,5-Dichlorobenzeneboronic acidHCID 2773371—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물4-Chloro-6-(2,5-dichloro-phenyl)-pyrimidin-2-yl-amineHCID 8659459931.5%

반응 단계

To a mixture of 4,6-dichloro-pyrimidin-2-yl-amine (0.625 g, 3.81 mmol), 2,5-dichloro-phenyl boronic acid (0.726 g, 3.81 mmol), palladium (II) acetate (0.128 g, 0.57 mmol) and triphenylphosphine (0.30 g, 1.14 mmol) was added a solution of sodium carbonate (2.0 g, 19.0 mmol) in water (5 ml) followed by glyme (20 ml). The mixture was stirred under an argon atmosphere for 6 hours. Filtration and concentration of the filtrate yielded the crude product which was purified by flash chromatography on silica gel eluting with ethyl acetate-chloroform (1:8). After evaporation of solvents under reduced pressure, the residue was dissolved in ethanol (100 ml) and stirred while a solution of hydrogen chloride in dioxane (4.0 M, 2.5 ml) was added. After evaporation of volatiles under reduced pressure, the residue was treated with ethyl acetate (25 ml) and stirred for 16 hours. Filtration provided the hydrochloride salt of 4-chloro-6-(2,5-dichloro-phenyl)-pyrimidin-2-yl-amine (0.330 g, 28% yield) as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419984B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-2531632c8b87439aa6a3f8e3c1770705
출처 메모uspto-grants-2008_09