돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 415444생성일: 2026년 10월 24일

4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidine → N-(3-methoxy-1H-pyrazol-5-yl)-2-(methylthio)-6-(trifluoromethyl)pyrimidin-4-amine

https://huagongshe.com/ko/reaction/415444

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidineHCID 248063—
반응물HCID 178493289HCID 178493289—
용매EthanolHCID 702—
생성물N-(3-methoxy-1H-pyrazol-5-yl)-2-(methylthio)-6-(trifluoromethyl)pyrimidin-4-amineHCID 6662454521.5%

반응 조건

온도90 °C

반응 단계

To a solution of 4-chloro-2-(methylthio)-6-(trifluoromethyl)pyrimidine (2.29 g) in absolute ethanol (50 mL) was added DIEPA (4.4 mL) and 5-methoxy-1H-pyrazol-3-amine hydrogen chloride salt (1.46 g). The resulting solution was heated at 90° C. for over night. The solvent was evaporated under reduced pressure. The crude compound was purified by Gilson (10-60% MeCN/H2O, 15 minutes) to give N-(3-methoxy-1H-pyrazol-5-yl)-2-(methylthio)-6-(trifluoromethyl)pyrimidin-4-amine as solid (0.64 g). m/z 306. N-(3-methoxy-1H-pyrazol-5-yl)-2-(methylthio)-6-(trifluoromethyl)pyrimidin-4-amine (240 mg) was dissolved in methylene chloride (5 mL), MCPBA (529 mg) was added. The resulting solution was stirred at room temperature for 0.5 hours and separate between methylene chloride and saturated sodium carbonate water solution. The organic layer was dried and solvent was removed under reduced pressure and low temperature. The crude product (270 mg) was carried on to do next step without further purification. m/z 338.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088784B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-a3834143e34d4281a1cb9762b51be000
출처 메모uspto-grants-2012_01