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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 968900생성일: 2026년 10월 24일

Phosphorus oxychloride → Methyl 2-chloro-4-(4-fluorophenyl)-6-isopropylpyrimidine-5-carboxylate

https://huagongshe.com/ko/reaction/968900

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxychlorideHCID 24813—
반응물Sodium BicarbonateHCID 516892—
반응물Methyl 6-(4-fluorophenyl)-1,2-dihydro-4-(1-methylethyl)-2-oxo-5-pyrimidinecarboxylateHCID 178496923—
생성물Methyl 2-chloro-4-(4-fluorophenyl)-6-isopropylpyrimidine-5-carboxylateHCID 1122057197.3%

반응 조건

온도103 °C

반응 단계

In a 25 mL-volume glass flask equipped with a stirrer, a thermometer and a reflux condenser were placed 1.00 g (3.43 mmol.) of 4-(4-fluorophenyl)-2-hydroxy-6-isopropyl-5-methoxycarbonylpyrimidine and 3.4 mL (3.7 mmol.) of phosphorus oxychloride. The mixture was heated to 100-106° C. for 1.5 hours under refluxing, to carry out reaction. After the reaction was complete, the reaction mixture was cooled to room temperature, and poured into an ice/water mixture. The resulting aqueous mixture was neutralized with a saturated aqueous sodium hydrogen carbonate solution. The neutralized aqueous mixture was extracted with ethyl acetate. The ethyl acetate portion was separated, washed with a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The dried ethyl acetate portion was filtered and concentrated under reduced pressure, to obtain 1.03 g of 2-chloro-4-(4-fluorophenyl)-6-isopropyl-5-methoxycarbonylpyrimidine as a colorless crystalline product having the below-mentioned characteristics. The yield was 97% (based on the amount of 4-(4-fluorophenyl)-2-hydroxy-6-isopropyl-5-methoxycarbonylpyrimidine).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07304156B2
출처 데이터셋uspto-grants-2007_12
ORD IDord-03e56e2d78cc4c30bd7b8bbbed45d799
출처 메모uspto-grants-2007_12