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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1369964생성일: 2026년 10월 24일

Toluene → Methyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylate

https://huagongshe.com/ko/reaction/1369964

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물N-cyano-N-methylmethanesulphonamideHCID 10219456—
반응물HCID 178500902HCID 178500902—
촉매Titanium TetrachlorideHCID 24193—
용매WaterHCID 962—
생성물Methyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylateHCID 992982180.3%

반응 조건

온도110 °C

반응 단계

10.0 g (37.7 mmol) of methyl 2-[1-amino-1-(4-fluorophenyl)methylene]-4-methyl-3-oxopentanoate were introduced into 50 ml of toluene together with 10.17 g (75.4 mmol) of N-cyano-N-methylmethanesulphonamide and the mixture was treated at room temperature with 3.61 g (18.9 mmol) of titanium tetrachloride. The reaction progressed exothermically. The red-orange-coloured suspension was heated to 110° C. and stirred for 4.5 h. It was then cooled to room temperature and treated with 30 ml of water. The organic phase was separated off and the aqueous phase was extracted with ethyl acetate (30 ml). The combined organic phases were washed with 30 ml of water and dried over magnesium sulphate. After filtering and concentrating the solution in a water-jet vacuum and drying in vacuo, 11.54 g of crude product were obtained in the form of a tacky oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06579984B1
출처 데이터셋uspto-grants-2003_06
ORD IDord-a88c99e6b92846ce873a7ea338fac563
출처 메모uspto-grants-2003_06