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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38044생성일: 2026년 10월 25일

4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidine → 2-Methylsulfanyl-4-trifluoromethyl-6-[(S)-3-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidin-1-yl]-pyrimidine

https://huagongshe.com/reaction/38044

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidineHCID 248063—
반응물Potassium FluorideHCID 522689—
반응물(S)-3-(2-Trifluoromethyl-benzenesulfonyl)-pyrrolidineHCID 67497015—
용매AcetonitrileHCID 6342—
생성물2-Methylsulfanyl-4-trifluoromethyl-6-[(S)-3-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidin-1-yl]-pyrimidineHCID 86664757—

반응 단계

(S)-3-(2-Trifluoromethyl-benzenesulfonyl)-pyrrolidine (500 mg) was dissolved in acetonitrile (3.5 mL) in a microwave tube. 4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidine (450 mg), TEA (0.75 mL) and KF (10 mg) were added. The reaction mixture was irradiated in the microwave oven at 150° C. for 1.5 h. The reaction mixture was evaporated to dryness and purified by flash chromatography (50 g silica gel, ethyl acetate/n-heptane:0:1→1:0) to yield a light yellow oil (790 mg; 94%) MS: m/z=472.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524710B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-426f1c2152a64c8bbebd23636fbb52b5
출처 메모uspto-grants-2013_09