돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501881생성일: 2026년 10월 27일

Tert-Butyl hypochlorite → 2-[(4,6-Dimethoxypyrimidin-2-yl)-methylthiomethyl]-6-methoxymethylaniline

https://huagongshe.com/reaction/501881

반응식

참여 물질

역할이름HCID투입량
반응물Tert-Butyl hypochloriteHCID 521297—
반응물Sodium MethoxideHCID 10942334—
반응물2-(Methoxymethyl)anilineHCID 12334306—
반응물2-Methylthiomethyl-4,6-dimethoxypyrimidineHCID 57428123—
용매MethanolHCID 887—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2-[(4,6-Dimethoxypyrimidin-2-yl)-methylthiomethyl]-6-methoxymethylanilineHCID 1672631458.8%

반응 조건

온도-70 °C

반응 단계

2-Methoxymethylaniline (0.68 g, 4.96 mmol) was dissolved in dichloromethane (50 ml) and the solution was cooled to −70° C. To the cooled solution a solution of tert-butyl hypochlorite (0.54 g, 4.96 mmol) in dichloromethane (1 ml) was added dropwise and the solution was stirred at −70° C. for 10 minutes. To the obtained reaction solution a solution of 2-methylthiomethyl-4,6-dimethoxypyrimidine (0.893 g, 4.46 mmol) in dichloromethane (5 ml) was added dropwise and the solution was stirred at −70° C. for 30 minutes. To the obtained reaction solution a 28% methanol solution of sodium methoxide (4 ml) was added and the solution was stirred until its temperature reached room temperature. Water was added to the reaction solution and the organic layer was separated. The water layer was further extracted twice with dichloromethane. The organic layer was washed with water and dried. Then dichloromethane was distilled off under reduced pressure and the obtained oily substance was purified by column chromatography using 1:6 mixed solvent of ethyl acetate and hexane as eluent to obtain 2-[(4,6-dimethoxypyrimidin-2-yl)-methylthiomethyl]-6-methoxymethylaniline (0.88 g, yield 53%) as oily substance;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772395B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-8f4ca55198c64fdfb6527531970c3dc7
출처 메모uspto-grants-2010_08