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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 411228생성일: 2026년 10월 23일

Diethyl (ethoxymethylene)malonate → Ethyl 4-Hydroxy-6,8-dimethyl-1,7-naphthyridine-3-carboxylate

https://huagongshe.com/ko/reaction/411228

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl (ethoxymethylene)malonateHCID 6871—
반응물2,6-Dimethyl-3-pyridylamineHCID 76964—
용매O-XyleneHCID 7237—
생성물Ethyl 4-Hydroxy-6,8-dimethyl-1,7-naphthyridine-3-carboxylateHCID 2239715930%

반응 단계

A mixture of 2,6-dimethyl-3-aminopyridine (0.85 g) and diethyl ethoxymethylenemalonate (1.53 g) is heated at 135° C. in xylene (30 mL) for 2 h allowing for removal of ethanol. After the solvent is removed, the mixture is suspended in diphenyl ether (15 mL). The mixture is then heated to reflux with removal of ethanol for 30 min. The reaction mixture is cooled to room temperature and hexanes (20 mL) is added. The resulting precipitate is filtered, washed with diethyl ether (2×10 mL) and dried to give 0.5 g (30%) of the title compound as a brown solid. Physical chracteristics: MS (ESI+) m/z 247 (M+H)+; 1H NMR (DMSO) δ 8.67, 7.97,4.38, 2.85,2.67, 1.40.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06559145B2
출처 데이터셋uspto-grants-2003_05
ORD IDord-49a08db830dd47799eff0645827e3280
출처 메모uspto-grants-2003_05