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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 336961생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/336961

반응식

참여 물질

역할이름HCID투입량
반응물Triethyl PhosphateHCID 6535—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물(3-Trifluoromethylphenyl)ureaHCID 25712—
반응물Allyl acetoacetateHCID 70701—
반응물4-Formyl-3-[(1-methylethyl)sulfonyl]benzonitrileHCID 58133848—
용매tert-Butyl methyl etherHCID 15413—
생성물Allyl (rac)-4-{4-cyano-2-[(1-methylethyl)sulfonyl]phenyl}-6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylateHCID 58133777—

반응 조건

온도90 °C

반응 단계

The reaction was carried out under argon. Triethyl phosphate (1.049 g, 5.76 mmol) and diphosphorus pentoxide (0.454 g) were stirred at 40° C. overnight. The mixture was then diluted with MTBE (25 ml), and 4-formyl-3-[(1-methylethyl)sulfonyl]benzonitrile (0.759 g, 3.2 mmol), 1-[3-(tri-fluoromethyl)phenyl]urea (0.653 g, 3.2 mmol) and allyl acetoacetate (0.682 g, 4.8 mmol; 1.5 eq.) were added. The mixture was stirred under reflux for 6 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 (2×10 ml). This gave 1.25 g (48% of theory) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889700B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-4fe3ec2edc72435584a961b47e28687d
출처 메모uspto-grants-2014_11