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HRID 226950作成日:2026年10月26日

Dimethylformamide → 3-(3,4-Dimethyl-benzoyl)-1-(5-methyl-isoxazol-3-ylmethyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/226950

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物AcetonitrileHCID 6342—
反応物Sodium hydrideHCID 24758—
反応物3-(Chloromethyl)-1,2,4-oxadiazoleHCID 2735765—
反応物3-(3,4-Dimethyl-benzoyl)-1H-quinolin-4-oneHCID 57754515—
生成物3-(3,4-Dimethyl-benzoyl)-1-(5-methyl-isoxazol-3-ylmethyl)-1H-quinolin-4-oneHCID 16730933—

反応条件

温度80 °C

反応手順

26 mg (0.65 mmol) of sodium hydride (60%) was suspended in 3 mL of anhydrous dimethylformamide and to it was added 138.7 mg (0.50 mmol) of 3-(3,4-dimethyl-benzoyl)-2,3-dihydro-1H-quinolin-4-one 3a and the resultant mixture was stirred at rt for 30 min. Then 77.4 mg (0.65 mmol) of 3-chloromethyl-1,2,4-oxadiazole was added to the reaction solution and the mixture was stirred at 80° C. for 1 h. The reaction solution was quenched by the addition of 10 mL of water. The crude product precipitated out of solution and was isolated by filtration. Purification of the crude product by flash chromatography provided 55 mg of 4cc as a colorless solid: LC-MSD, m/z for C23H20N2O3, [M+H]+=373.4, [M+2H]+=374.4; Reverse phase HPLC (gradient acetonitrile 0.1% TFA 20-95% in 4 min) retention time =2.639 min; 1H NMR (400 MHz, CDCl3/HCl): δ 2.30 (d, 6H), 2.36 (s, 3H), 5.38 (s, 2H), 5.90 (s, 1H), 7.15 (d, 1H), 7.42 (t, 1H), 7.50-7.68 (m, 4H), 8.27 (s, 1H), 8.44 (d, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557213B2
出典データセットuspto-grants-2009_07
ORD IDord-b1b7d3dc6c0d410b90c1fceaad4c1d8e
出典メモuspto-grants-2009_07