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HRID 35818생성일: 2026년 10월 24일

Chloromethyl ethyl ether → 2-(4,6-dimethoxypyrimidin-2-yl)-N-methoxymethyl-3-methyl-N-methylsulfonylbutyric acid amide

https://huagongshe.com/ko/reaction/35818

반응식

참여 물질

역할이름HCID투입량
반응물Chloromethyl ethyl etherHCID 18523—
반응물Sodium hydrideHCID 24758—
반응물2-(4,6-dimethoxypyrimidin-2-yl)-3-methyl-N-methylsulfonylbutyric acid amideHCID 15239783—
용매DimethylformamideHCID 6228—
생성물2-(4,6-dimethoxypyrimidin-2-yl)-N-methoxymethyl-3-methyl-N-methylsulfonylbutyric acid amideHCID 15239784—

반응 단계

2.0 of 2-(4,6-dimethoxypyrimidin-2-yl)-3-methyl-N-methylsulfonylbutyric acid amide was placed in a round bottom flask, and was dissolved in 50 ml of DMF. To the resultant solution, was gradually added 0.28 g of 60% sodium hydride, and the mixture was stirred at room temperature for one hour. Thereafter, 1.0 g of chloromethyl ethyl ether was added dropwise to the resultant mixture, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was then poured into ice water, and was extracted with 200 ml of diethyl ether, followed by drying with anhydrous sodium sulfate. After filtrating the inorganic salt, the solvent was distilled off under reduced pressure. An only product thus obtained was purified by silica gel column chromatography (developing solvent: N-hexane/ethyl acetate=10/1) to obtain 1.8 g of the aimed product of colorless transparent viscous liquid (yield=78.3%) having a refractive index (n20/D) of 1.4976.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05411934
출처 데이터셋uspto-grants-1995_05
ORD IDord-b68c3be258a141f9ab74387b65549ad7
출처 메모uspto-grants-1995_05