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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12712생성일: 2026년 10월 25일

Potassium Carbonate → 5-(2-Fluoro-3-pyridinyl)-2,4-bis(methyloxy)pyrimidine

https://huagongshe.com/reaction/12712

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Boronic AcidHCID 61668—
반응물5-Bromo-2,4-dimethoxypyrimidineHCID 255719—
반응물2-Fluoropyridine-3-boronic acidHCID 2783270—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물5-(2-Fluoro-3-pyridinyl)-2,4-bis(methyloxy)pyrimidineHCID 5899415593.1%

반응 조건

온도90 °C

반응 단계

To a mixture of 5-bromo-2,4-bis(methyloxy)pyrimidine (Prep86, 3 g, 13.70 mmol), 2-fluoropyridine-3-boronic acid (1.930 g, 13.70 mmol) and Pd(PPh3)4 (0.791 g, 0.685 mmol), dry 1,4-Dioxane (45 ml) was added followed by potassium carbonate 1M solution (27.4 ml, 27.4 mmol). The mixture was degassed with Argon and then heated at 100° C. for 1 h (internal T˜90° C.). Then the mixture was cooled down to ambient, further 1 eq of boronic acid (1.930 g, 13.70 mmol) followed by 5 mol % of PdTetrakis (0.791 g, 0.685 mmol) were added and the mixture heated at 100° C. for two 2 h. The reaction mixture was cooled down to room temperature, taken up with water and AcOEt. The aqueous layer was back extracted with AcOEt. The combined organics were dried over Na2SO4 and evaporated to dryness. The crude material was purified by SiO2 flash chromatography eluting with Cy/EA 8/2 to get the title compound as white solid (3 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727988B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c4c1cbbe3d4c4342ab9166f0952850e1
출처 메모uspto-grants-2010_06