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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1366245생성일: 2026년 10월 27일

(3-Trifluoromethylphenyl)urea → Allyl 4-(4-cyanophenyl)-6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylate

https://huagongshe.com/reaction/1366245

반응식

참여 물질

역할이름HCID투입량
반응물(3-Trifluoromethylphenyl)ureaHCID 25712—
반응물4-CyanobenzaldehydeHCID 66042—
반응물Allyl acetoacetateHCID 70701—
용매1,4-DioxaneHCID 31275—
생성물Allyl 4-(4-cyanophenyl)-6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylateHCID 59684802—

반응 단계

45.0 g ethyl polyphosphate are dissolved in 150 ml dioxane, 15.0 g (73.5 mmol) N-[3-(trifluoromethyl)phenyl]urea, 19.3 g (147 mmol) 4-cyanobenzaldehyde and 20.9 g (147 mmol) allyl aceto-acetate are added, and the mixture is stirred under reflux overnight. Volatiles are evaporated in vacuo, the remainder is dissolved in ethyl acetate and sequentially washed with saturated sodium hydrogencarbonate, sodium hydrogensulfite and sodium chloride solution. The organic phase is dried over magnesium sulfate, filtered and evaporated to dryness in vacuo. The crude product is purified by column chromatography over silica gel (eluent: cyclohexane/ethyl acetate).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07893073B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-a18e6d31b094488b84accffe4ffc13aa
출처 메모uspto-grants-2011_02