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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1360044생성일: 2026년 10월 25일

Sodium hydride → N-(4-iodophenyl)-N-(2-methoxyethyl)pyrimidin-2-amine

https://huagongshe.com/reaction/1360044

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-Bromoethyl methyl etherHCID 80972—
반응물N-(4-iodophenyl)pyrimidin-2-amineHCID 57762548—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물N-(4-iodophenyl)-N-(2-methoxyethyl)pyrimidin-2-amineHCID 57762539—

반응 단계

Under an argon atmosphere, 2-bromoethylmethyl ether (0.14 ml) and sodium hydride (48 mg) were added to a solution of N-(4-iodophenyl)pyrimidin-2-amine (300 mg) in anhydrous DMF (1 ml), and the resulting mixture was stirred at room temperature overnight. Saturated brine was added to the reaction solution and the resulting mixture was extracted with chloroform, followed by drying the organic layer over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent:hexane/chloroform=1/10) to obtain N-(4-iodophenyl)-N-(2-methoxyethyl)pyrimidin-2-amine (233 mg). NMR (H1, CDCl3): δ 3.32 (3H, s), 3.63 (2H, t, J=5.9 Hz), 4.14 (2H, t, J=5.9 Hz), 6.59 (1H, t, J=4.9 Hz), 7.09-7.13 (2H, m), 7.70-7.73 (2H, m), 8.32 (2H, d, J=4.9 Hz)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879837B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-2d0a123732734fd38e3e69a597ef40d5
출처 메모uspto-grants-2011_02