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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226964생성일: 2026년 10월 24일

m-Xylyl bromide → 3-(3,4-dimethyl-benzoyl)-6-fluoro-1-(3-methyl-benzyl)-1H-quinolin-4-one

https://huagongshe.com/ko/reaction/226964

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참여 물질

역할이름HCID투입량
반응물m-Xylyl bromideHCID 12099—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물3-(3,4-dimethylbenzoyl)-6-fluoroquinolin-4(1H)-oneHCID 4606570—
용매TetrahydrofuranHCID 8028—
생성물3-(3,4-dimethyl-benzoyl)-6-fluoro-1-(3-methyl-benzyl)-1H-quinolin-4-oneHCID 1673124677.3%

반응 조건

온도60 °C

반응 단계

Compound 4uu was prepared following the procedure outlined in Step 3 of Example 1. Briefly described here, 0.050 g (0.169 mmol) of 3-(3,4-dimethyl-benzoyl)-6-fluoro-1H-quinolin-4-one 3j, 0.4 mL of potassium hexamethyldisilazide (0.5 M in toluene, 0.203 mmol) and 37.6 mg (0.203 mmol) of 3-methylbenzyl bromide were combined in 1.5 mL of tetrahydrofuran and heated at 60° C. for 3 h. Purification of the crude product using flash chromatography (30-50% ethyl acetate in hexane) yielded 52.2 mg of 3-(3,4-dimethyl-benzoyl)-6-fluoro-1-(3-methyl-benzyl)-1H-quinolin-4-one as a white solid 4uu: LC-MSD, m/z for C26H22FNO2, [M+H]=400.5; Reverse phase HPLC gradient, 20-95% acetonitrile with 0.1% TFA in 4 minutes, retention time=2.9 min; 1H NMR (400 MHz, CDCl3): δ 8.26 (1H, s), 8.11 (1H, m), 7.64 (1H, s), 7.56 (1H, m), 7.38 (1H, m), 7.32-7.23 (2H, m), 7.18 (1H, m), 7.15 (1H, m), 6.97 (2H, m), 5.37 (2H, s), 2.33 (3H, s), 2.32 (3H, s), 2.31 (3H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557213B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-be70811647bd42f78515e1db5b8d4303
출처 메모uspto-grants-2009_07