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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethyl PhosphateHCID 6535—
EduktPhosphorus oxide (P4O10)HCID 14812—
Edukt(3-Trifluoromethylphenyl)ureaHCID 25712—
EduktAllyl acetoacetateHCID 70701—
Edukt3-(Ethylsulfonyl)-4-formylbenzonitrileHCID 58133833—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
ProduktAllyl(rac)-4-[4-cyano-2-(ethylsulfonyl)phenyl]-6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylateHCID 58133859—

Reaktionsbedingungen

Temperatur90 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889700B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-93fb55141b164c87a44395773e928ac2
Quellennotizuspto-grants-2014_11