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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226978생성일: 2026년 10월 26일

Sodium hydride → 1-(6-Bromo-pyridin-2-ylmethyl)-3-(3,4-dimethyl-benzoyl)-6,8-dimethyl-1H-[1,7]naphthyridin-4-one

https://huagongshe.com/reaction/226978

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-Bromo-6-(bromomethyl)pyridineHCID 12954796—
반응물3-(3,4-Dimethyl-benzoyl)-6,8-dimethyl-1H-[1,7]naphthyridin-4-oneHCID 57754774—
용매DimethylformamideHCID 6228—
생성물1-(6-Bromo-pyridin-2-ylmethyl)-3-(3,4-dimethyl-benzoyl)-6,8-dimethyl-1H-[1,7]naphthyridin-4-oneHCID 5775472912.1%

반응 단계

Experimental conditions analogous to described for Step 3 of Example 1 were used with 42 mg (0.137 mmol) of 3-(3,4-Dimethyl-benzoyl)-6,8-dimethyl-1H-[1,7]naphthyridin-4-one, 6 mg (0.165 mmol, 60% dispersion in oil) of sodium hydride, 41.3 mg (0.165 mmol) of 2-bromo-6-bromomethyl-pyridine and 1.5 mL of N,N-dimethylformamide. The crude brown solid was purified by flash column chromatography using 30-100% ethyl acetate in hexane to yield 7.9 mg of 1-(6-Bromo-pyridin-2-ylmethyl)-3-(3,4-dimethyl-benzoyl)-6,8-dimethyl-1H-[1,7]naphthyridin-4-one as an off white solid. LC-MSD, m/z for C25H22BrN3O2 [M+H]: 477.37 LC retention time on HPLC, C18 column gradient 20-95% acetonitrile with 0.1% TFA in 4 minutes: 2.9 min

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557213B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-c7462869f20d466fbc008b61ea7225a6
출처 메모uspto-grants-2009_07