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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36803생성일: 2026년 10월 24일

Dimethyl Sulfate → 3-(4-chloro-5-ethylsulfonylamino-2-fluorophenyl)-1-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione

https://huagongshe.com/ko/reaction/36803

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfateHCID 6497—
반응물Potassium CarbonateHCID 11430—
반응물3-(4-chloro-5-ethylsulfonylamino-2-fluorophenyl)-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedioneHCID 11112479—
용매AcetoneHCID 180—
생성물3-(4-chloro-5-ethylsulfonylamino-2-fluorophenyl)-1-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedioneHCID 15405304118.3%

반응 단계

1.00 g (2.41 mmol) of 3-(4-chloro-5-ethylsulfonylamino-2-fluorophenyl)-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione was dissolved in 10 ml of acetone, and 0.17 g (1.20 mmol) of anhydrous potassium carbonate and 0.23 ml (2.41 mmol) of dimethyl sulfate were added thereto and the reaction was continued for 1.5 hours. After acetone was distilled off, the reaction product was dissolved in ethyl acetate, washed with water and saturated saline solution, and dried over anhydrous sodium sulfate. Thereafter the ethyl acetate was distilled off to obtain a crude product. The crude product was recrystallized from chloroformdiethyl ether, thereby obtaining 0.61 g of the objective product (yield: 59%) in the form of light yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05416236
출처 데이터셋uspto-grants-1995_05
ORD IDord-30fbf4b7c40d4fae8e27479de6bcd0ff
출처 메모uspto-grants-1995_05