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HRID 12712作成日:2026年10月26日

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

https://huagongshe.com/reaction/12712

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Boronic AcidHCID 61668—
反応物5-Bromo-2,4-dimethoxypyrimidineHCID 255719—
反応物2-Fluoropyridine-3-boronic acidHCID 2783270—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
生成物5-(2-Fluoro-3-pyridinyl)-2,4-bis(methyloxy)pyrimidineHCID 5899415593.1%

反応条件

温度90 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727988B2
出典データセットuspto-grants-2010_06
ORD IDord-c4c1cbbe3d4c4342ab9166f0952850e1
出典メモuspto-grants-2010_06