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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 336942생성일: 2026년 10월 25일

Triethyl Phosphate → Allyl(rac)-4-[4-cyano-2-(methylsulfanyl)phenyl]-6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylate

https://huagongshe.com/reaction/336942

반응식

참여 물질

역할이름HCID투입량
반응물Triethyl PhosphateHCID 6535—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물(3-Trifluoromethylphenyl)ureaHCID 25712—
반응물Allyl acetoacetateHCID 70701—
반응물4-Formyl-3-(methylsulfanyl)benzonitrileHCID 58133742—
용매tert-Butyl methyl etherHCID 15413—
생성물Allyl(rac)-4-[4-cyano-2-(methylsulfanyl)phenyl]-6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylateHCID 44133410—

반응 단계

The reaction was carried out under argon. Triethyl phosphate (1.46 g, 8.04 mmol) and diphosphorus pentoxide (761 mg, 5.36 mmol) were stirred at 50° C. overnight. The mixture was then diluted with MTBE (27 ml), and 4-formyl-3-(methylsulfanyl)benzonitrile (1.18 g, 6.70 mmol; Example 9A), 1-[3-(trifluoromethyl)phenyl]urea (1.37 g, 6.70 mmol) and allyl acetoacetate (1.43 g, 10.1 mmol) were added. The mixture was stirred under reflux overnight. For work-up, the solvent was removed under reduced pressure and the residue was suspended in diethyl ether and then filtered of with suction. This gave 978 mg (19% of theory) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889700B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-95fe4ec652974181a0ac0a2ca4320375
출처 메모uspto-grants-2014_11