HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl Phosphate | HCID 6535 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | (3-Trifluoromethylphenyl)urea | HCID 25712 | — |
| Reactant | Allyl acetoacetate | HCID 70701 | — |
| Reactant | 4-Formyl-3-(methylsulfanyl)benzonitrile | HCID 58133742 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Allyl(rac)-4-[4-cyano-2-(methylsulfanyl)phenyl]-6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylate | HCID 44133410 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889700B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-95fe4ec652974181a0ac0a2ca4320375 |
| Source note | uspto-grants-2014_11 |