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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethyl Phosphate | HCID 6535 | — |
| 반응물 | Phosphorus oxide (P4O10) | HCID 14812 | — |
| 반응물 | (3-Trifluoromethylphenyl)urea | HCID 25712 | — |
| 반응물 | Allyl acetoacetate | HCID 70701 | — |
| 반응물 | 3-(Ethylsulfonyl)-4-formylbenzonitrile | HCID 58133833 | — |
| 용매 | tert-Butyl methyl ether | HCID 15413 | — |
| 생성물 | Allyl(rac)-4-[4-cyano-2-(ethylsulfonyl)phenyl]-6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylate | HCID 58133859 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08889700B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_11 |
|---|
| ORD ID | ord-93fb55141b164c87a44395773e928ac2 |
|---|
| 출처 메모 | uspto-grants-2014_11 |
|---|