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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 224721생성일: 2026년 10월 24일

Diethyl Ether → Ethyl 8-allyl-5-hydroxy-2-(methylthio)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxylate

https://huagongshe.com/ko/reaction/224721

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Ethyl 2-methylsulfanyl-4-(prop-2-enylamino)pyrimidine-5-carboxylateHCID 295704—
반응물2-Ethylpropanedioyl dichlorideHCID 10920924—
생성물Ethyl 8-allyl-5-hydroxy-2-(methylthio)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxylateHCID 54729613—

반응 단계

To a solution of 25.3 g. (0.1 mole) of 4-allylamino-2-methylthio-5-pyrimidine carboxylic acid ethyl ester in 400 ml. of anhydrous diethyl ether was added 7.5 g. (0.005 mole) of ethyl malonyl chloride. The mixture was stirred at room temperature for 3 hours. The mixture was filtered and the filtrate was evaporated in a rotary evaporator. The residue was dissolved in 15 ml. of ethanol and this solution was added to a solution of 2.3 g. (0.1 g. atom) of sodium in 200 ml. of ethanol. The mixture was stirred at room temperature for 5 minutes and was diluted with water, acidified with glacial acetic acid and was extracted with 150 ml. of diethyl ether. The ether layer was dried over magnesium sulfate, filtered and was acidified with gaseous hydrogen chloride. The mixture was filtered and the filtrate was cooled in ice. The precipitate which formed was collected and was recrystallized from ethyl acetate to give 0.2 g. of product--m.p. 134°-136° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04233446
출처 데이터셋uspto-grants-1980_11
ORD IDord-226c5bb0675d4c8c9100f583d57bd51c
출처 메모uspto-grants-1980_11