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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 336954생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/336954

반응식

참여 물질

역할이름HCID투입량
반응물Triethyl PhosphateHCID 6535—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물(3-Trifluoromethylphenyl)ureaHCID 25712—
반응물Allyl acetoacetateHCID 70701—
반응물3-(Ethylsulfonyl)-4-formylbenzonitrileHCID 58133833—
용매tert-Butyl methyl etherHCID 15413—
생성물Allyl(rac)-4-[4-cyano-2-(ethylsulfonyl)phenyl]-6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylateHCID 58133859—

반응 조건

온도90 °C

반응 단계

The reaction was carried out under argon. Triethyl phosphate (0.718 g, 3.9 mmol) and diphosphorus pentoxide (0.511 g) were stirred at 40° C. overnight. The mixture was then diluted with MTBE (30 ml), and 4-formyl-3-(ethylsulfonyl)benzonitrile (0.88 g, 3.94 mmol), 1-[3-(trifluoromethyl)phenyl]urea (0.805 g, 3.94 mmol) and allyl acetoacetate (0.841 g, 5.91 mmol; 1.5 eq.) were added. The mixture was then stirred under reflux for 4 h. The reaction mixture was then concentrated by distillative removal of MTBE and subsequently heated at 90° C. for a further 2 h. For work-up, residual solvent was removed under reduced pressure, and the residue was suspended in MTBE (20 ml) and then filtered off with suction. The solid was washed with MTBE (10 ml). This gave 1.34 g (42% of theory) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889700B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-93fb55141b164c87a44395773e928ac2
출처 메모uspto-grants-2014_11