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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1498700생성일: 2026년 10월 26일

Tetrahydrofuran → 2,4-dimethoxy-7-(4-methoxy-3,5-dimethylphenyl)-1,6-naphthyridin-5(6H)-one

https://huagongshe.com/reaction/1498700

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물4-MethoxybenzonitrileHCID 70129—
반응물4,6-Dimethoxy-2-methyl-nicotinamideHCID 66661472—
반응물ButyllithiumHCID 178418339—
생성물2,4-dimethoxy-7-(4-methoxy-3,5-dimethylphenyl)-1,6-naphthyridin-5(6H)-oneHCID 2495970512%

반응 조건

온도0 °C

반응 단계

To a solution of 4,6-dimethoxy-2-methyl nicotinamide (2.0 g, 10.2 mmol) in THF (80 mL), n-butyl lithium (19.12 mL, 30.6 mmol, 1.6 M solution in hexane) was added slowly under nitrogen at −78° C. After completion of addition the mixture was stirred for 1 h at 0° C. Then cooled to −78° C. and a solution of 4-methoxy benzonitrile (1.65 g, 10.2 mmol) in THF (10 mL) was added quickly. The cooling bath was removed and the reaction mixture was allowed to warm to room temperature and stirred for 16 h at room temperature. Saturated NH4Cl solution was added with cooling. The organic layer was washed with water, brine, dried over Na2SO4 and concentrated to give crude product. The crude product was purified by chromatography using 50% ethyl acetate in hexane and then 2% methanol in ethyl acetate to give 2,4-dimethoxy-7-(4-methoxy-3,5-dimethylphenyl)-1,6-naphthyridin-5(6H)-one (410 mg, 12%), as a yellow solid. Selected data: MS (ES) m/z: 341.1; mp 262-263° C. (at decomposition).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09199990B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-da42ee9703ec450fb9a191dc415d2ba0
출처 메모uspto-grants-2015_12