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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1722975생성일: 2026년 10월 25일

Pyridine → 2-chloro-5-[3,6-dihydro-2,6-dioxo-3-methyl-4-trifluoromethyl-1(2H)-pyrimidinyl]-4-fluorophenyl chlorosulphate

https://huagongshe.com/reaction/1722975

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Sulfuryl chlorideHCID 24648—
반응물1-methyl-6-trifluoromethyl-3-(4-chloro-2-fluoro-5-hydroxyphenyl)-2,4(1H,3H)-pyrimidinedioneHCID 11267757—
용매DichloromethaneHCID 6344—
생성물2-chloro-5-[3,6-dihydro-2,6-dioxo-3-methyl-4-trifluoromethyl-1(2H)-pyrimidinyl]-4-fluorophenyl chlorosulphateHCID 20026087—

반응 단계

A solution of 10.16 g of 3-(4-chloro-2-fluoro-5 -hydroxyphenyl)-1-methyl-6 -trifluoromethyl-2,4 (1H,3H)-pyrimidinedione and 20.20 g of sulphuryl chloride in 100 ml of methylene chloride is treated with a solution of 3.56 g of pyridine in 10 ml of methylene chloride while stirring and cooling during 5 minutes. The temperature rises to 20° C. The reaction mixture is stirred at 20°-25° C. for 15 minutes, subsequently poured on to ice and stirred vigorously. The organic phase is washed throughly with water, dried over anhydrous sodium sulphate and evaporated to dryness under reduced pressure. The residue is recrystallized from diethyl ether/n-hexane. There is obtained 2-chloro-5-[3,6-dihydro-2,6-dioxo-3-methyl-4-trifluoromethyl-1(2H)-pyrimidinyl]-4-fluorophenyl chlorosulphate m.p. 133°-135° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04859229
출처 데이터셋uspto-grants-1989_08
ORD IDord-022611f6d05d4297949c64fd8b8d2105
출처 메모uspto-grants-1989_08