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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2232539생성일: 2026년 10월 24일

Water → Ethyl 2-(3-methoxyphenyl)-4-quinazolinepropionate

https://huagongshe.com/ko/reaction/2232539

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물m-Anisoyl chlorideHCID 74374—
반응물Ethyl 4-(2-aminophenyl)-4-oxobutanoateHCID 21283602—
용매ChloroformHCID 6212—
생성물Ethyl 2-(3-methoxyphenyl)-4-quinazolinepropionateHCID 13769245—

반응 단계

3-Methoxybenzoyl chloride (2.81 cc) is added at 5° C. to ethyl 3-(2-aminobenzoyl)propionate (2.21 g) and triethylamine (4.2 cc) in chloroform (25 cc). The mixture is left for 1 hour at room temperature (approximately 20° C.), water (25 cc) is added and the mixture decanted. The organic phase is evaporated under reduced pressure and the residue taken up with ammonium acetate (17 g). The mixture is brought to 100° C. for 7 hours and the acetic acid formed is then evaporated off under reduced pressure. The residue is poured into water (100 cc) and the aqueous phase extracted with ethyl acetate (3×50 cc). The aqueous phase is dried over magnesium sulphate, filtered and evaporated to dryness under reduced pressure. The residual product is chromatographed in silica gel with a cyclohexane/ethyl acetate (1:1 by volume) mixture as eluant. After recrystallization in ethanol, ethyl 2-(3-methoxyphenyl)-4-quinazolinepropionate (1.5 g), m.p. 70° C., is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04788204
출처 데이터셋uspto-grants-1988_11
ORD IDord-718be82b29314e4eb59ec196f96c8a45
출처 메모uspto-grants-1988_11