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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 626897생성일: 2026년 10월 25일

Sodium Carbonate → 2-Chloro-4-(5-ethoxy-2-fluoro-phenyl)-6-methyl-pyrimidine

https://huagongshe.com/reaction/626897

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2,4-Dichloro-6-methylpyrimidineHCID 79471—
반응물5-Ethoxy-2-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 16217468—
촉매HCID 178419050HCID 178419050—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물2-Chloro-4-(5-ethoxy-2-fluoro-phenyl)-6-methyl-pyrimidineHCID 9001539296.6%

반응 조건

온도80 °C

반응 단계

To a solution of 2,4-dichloro-6-methyl-pyrimidine (2.66 g, 16.31 mmol) and (5-ethoxy-2-fluoro-phenyl)boronic acid (2 g, 10.87 mmol) in 1,2-dimethoxyethane (25 mL) and water (15 mL) was added sodium carbonate (3.46 g, 32.62 mmol). This was degassed with nitrogen for 5 minutes. Bis(triphenylphosphine)palladium (II) dichloride (0.38 g, 0.54 mmol) was then added and the reaction was heated to 80° C. overnight. The solvent was evaporated and the residue was partitioned between water (300 mL) and EtOAc (300 mL). The organics were washed with brine (100 mL), dried over MgSO4 and concentrated in vacuo to afford a yellow oil. The material was purified using a Biotage SP4 eluting with 0 to 30% i-hexane/EtOAc and the product containing fractions were collected and the solvent evaporated to give a colourless solid (2.8 g) mainly 2-chloro-4-(5-ethoxy-2-fluoro-phenyl)-6-methyl-pyrimidine (D16)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09309254B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-43e6a028560a4eb59ea6b00184185984
출처 메모uspto-grants-2016_04