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HRID 626897作成日:2026年10月26日

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

https://huagongshe.com/reaction/626897

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物2,4-Dichloro-6-methylpyrimidineHCID 79471—
反応物5-Ethoxy-2-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 16217468—
触媒HCID 178419050HCID 178419050—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2-Chloro-4-(5-ethoxy-2-fluoro-phenyl)-6-methyl-pyrimidineHCID 9001539296.6%

反応条件

温度80 °C

反応手順

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)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09309254B2
出典データセットuspto-grants-2016_04
ORD IDord-43e6a028560a4eb59ea6b00184185984
出典メモuspto-grants-2016_04