HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336954Erstellt: 26. Oktober 2026
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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethyl Phosphate | HCID 6535 | — |
| Edukt | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Edukt | (3-Trifluoromethylphenyl)urea | HCID 25712 | — |
| Edukt | Allyl acetoacetate | HCID 70701 | — |
| Edukt | 3-(Ethylsulfonyl)-4-formylbenzonitrile | HCID 58133833 | — |
| Lösungsmittel | tert-Butyl methyl ether | HCID 15413 | — |
| Produkt | 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 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08889700B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-93fb55141b164c87a44395773e928ac2 |
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| Quellennotiz | uspto-grants-2014_11 |
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