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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22662생성일: 2026년 10월 24일

Pyridine → 2-(4-Fluorophenyl)-3-(2-methylsulfanyl-pyrimidin-4-yl)-3-oxo-propionic acid methyl ester

https://huagongshe.com/ko/reaction/22662

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2-(4-Fluorophenyl)-3-(2-methylsulfanyl-pyrimidin-4-yl)-3-hydroxypropionic acid methyl esterHCID 12991402—
촉매ChromiumHCID 23976—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물2-(4-Fluorophenyl)-3-(2-methylsulfanyl-pyrimidin-4-yl)-3-oxo-propionic acid methyl esterHCID 1299140343%

반응 단계

To a suspension of CrO3 in CH2Cl2 (300 mL) is added pyridine. The mixture is stirred vigorously for 1 hour at room temp. A solution of the crude 2-(4-fluorophenyl)-3-(2-methylsulfanyl-pyrimidin-4-yl)-3-hydroxypropionic acid methyl ester, 2, prepared above in CH2Cl2 (50 mL) is added dropwise to the chromium suspension. The reaction mixture is stirred at room temperature for 16 hours, diluted with ether (1 L) and filtered through a pad of Celite. The filtrate is concentrated in vacuo and the resulting residue is purified over silica (25% EtOAc/hexanes) to afford 3.7 g (43% yield) of the desired product as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849627B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-7097432dc3454a69a351135a03291a4a
출처 메모uspto-grants-2005_02