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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2058184생성일: 2026년 10월 27일

Diethyl Ether → Ethyl 1-allyl-4-hydroxy-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate

https://huagongshe.com/reaction/2058184

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물2-Ethylpropanedioyl dichlorideHCID 10920924—
반응물2-Allylamino-6-methylnicotinic acid methyl esterHCID 12818656—
생성물Ethyl 1-allyl-4-hydroxy-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylateHCID 54696182—

반응 단계

To a solution of 2.88 g. (0.015 mole) of 2-allylamino-6-methylnicotinic acid, methyl ester in 50 ml. of anhydrous diethyl ether was added 1.12 g. (0.0075 mole) of ethyl malonyl chloride. The mixture was stirred at room temperature for 4 hours. The mixture was filtered and the filtrate was evaporated in a rotary evaporator. The residue was dissolved in 5 ml. of ethanol and this solution was added to a solution of 0.23 g. (0.01 g. atoms) of sodium in 20 ml. of ethanol. The mixture was stirred at room temperature for 5 minutes. The mixture was diluted with water and was acidified with glacial acetic acid. The mixture was extracted with diethyl ether and the ether layer was dried over magnesium sulfate, filtered and was acidified with an etheral hydrochloric acid solution. The mixture was filtered and the filtrate was evaporated. The residue was recrystallized from heptane to give 10 mg. of the title compound, m.p. 110°-112° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04215123
출처 데이터셋uspto-grants-1980_07
ORD IDord-216b37b273a94c24813ca62556f22c59
출처 메모uspto-grants-1980_07