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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226950생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/226950

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물AcetonitrileHCID 6342—
반응물Sodium hydrideHCID 24758—
반응물3-(Chloromethyl)-1,2,4-oxadiazoleHCID 2735765—
반응물3-(3,4-Dimethyl-benzoyl)-1H-quinolin-4-oneHCID 57754515—
생성물3-(3,4-Dimethyl-benzoyl)-1-(5-methyl-isoxazol-3-ylmethyl)-1H-quinolin-4-oneHCID 16730933—

반응 조건

온도80 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557213B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-b1b7d3dc6c0d410b90c1fceaad4c1d8e
출처 메모uspto-grants-2009_07