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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42701생성일: 2026년 10월 24일

Triethylamine → 6-[Allyl(methyl)amino]-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde

https://huagongshe.com/ko/reaction/42701

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물N-MethylallylamineHCID 69391—
반응물6-Chloro-5-formyl-1,3-dimethyluracilHCID 319971—
용매EthanolHCID 702—
생성물6-[Allyl(methyl)amino]-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehydeHCID 86658689—

반응 단계

To a stirred solution of 6-chloro-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde (0.500 g, 2.47 mmol) and triethyl-amine (0.52 ml, 3.71 mmol) in dry ethanol (10 ml), N-methylprop-2-en-1-amine (0.36 ml, 3.71 mmol) was added under argon. The resulting mixture was stirred at room temperature under argon overnight. After evaporation of the solvent in vacuo, water (15 ml) was added to the yellow oily residue, and the mixture was extracted with dichloromethane (4×15 ml). The combined organic phases were dried over anhydrous MgSO4. The solvent was evaporated in vacuo, and the crude product was purified by crystallization from a mixture of cyclohexane:isopropyl alcohol (4:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536210B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-cc7929173e2d446b981067cd1f9e794d
출처 메모uspto-grants-2013_09