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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36845생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/36845

반응식

참여 물질

역할이름HCID투입량
반응물Chloromethyl Methyl EtherHCID 7864—
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 1523978479%

반응 단계

2.0 g of 2-(4,6-dimethoxypyrimidin-2-yl)-3-methyl-N-methylsulfonylbutyric acid amide was placed in a round bottomed 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 methyl 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 oily product thus obtained was purified by silica gel column chromatography (developing solvent: N-hexane/ethyl acetate=10/l ) to obtain 1.8 g of the aimed product of colorless transparent viscous liquid (yield=78.3%) having a refractive index (nD20) of 1.4976.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05418212
출처 데이터셋uspto-grants-1995_05
ORD IDord-ca31222bec234d1980fa24b5aabbc145
출처 메모uspto-grants-1995_05