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HRID 336954作成日:2026年10月25日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Triethyl PhosphateHCID 6535—
反応物Phosphorus oxide (P4O10)HCID 14812—
反応物(3-Trifluoromethylphenyl)ureaHCID 25712—
反応物Allyl acetoacetateHCID 70701—
反応物3-(Ethylsulfonyl)-4-formylbenzonitrileHCID 58133833—
溶媒tert-Butyl methyl etherHCID 15413—
生成物Allyl(rac)-4-[4-cyano-2-(ethylsulfonyl)phenyl]-6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylateHCID 58133859—

反応条件

温度90 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889700B2
出典データセットuspto-grants-2014_11
ORD IDord-93fb55141b164c87a44395773e928ac2
出典メモuspto-grants-2014_11