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HRID 505908作成日:2026年10月25日

Potassium Carbonate → 2-((6-chloro-3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methyl)-4-Fluorobenzonitrile

https://huagongshe.com/reaction/505908

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6-chloro-3-methylpyrimidine-2,4(1H,3H)-dioneHCID 96141—
反応物2-(Bromomethyl)-4-fluorobenzonitrileHCID 21984990—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物2-((6-chloro-3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methyl)-4-FluorobenzonitrileHCID 2308935860%

反応条件

温度60 °C

反応手順

A mixture of crude 3-methyl-6-chlorouracil (0.6 g, 3.8 mmol), 2-bromomethyl-4-fluorobenzonitrile (0.86 g, 4 mmol) and K2CO3 (0.5 g, 4 mmol) in DMSO (10 mL) was stirred at 60° C. for 2 hours. The reaction was diluted with water and extracted with EtOAc. The organics were dried over MgSO4 and the solvent removed. The residue was purified by column chromatography. 0.66 g of the product was obtained (yield: 60%). 1H-NMR (400 MHz, CDCl3): δ 7.73 (dd, J=7.2, 8.4 Hz, 1H), 7.26 (d, J=4.0 Hz, 1H), 7.11-7.17 (m, 1H), 6.94 (dd, J=2.0, 9.0 Hz, 1H), 6.034 (s, 2H), 3.39 (s, 3H). MS (ES) [m+H] calc'd for C13H9ClFN3O2, 293.68; found 293.68.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07781584B2
出典データセットuspto-grants-2010_08
ORD IDord-511862c97ec448459cf14929e9bc6abe
出典メモuspto-grants-2010_08