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HRID 519643作成日:2026年10月24日

Trifluoroacetic anhydride → HCID 178438695、化合物

https://huagongshe.com/ja/reaction/519643

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic anhydrideHCID 9845—
反応物Sodium ThiosulfateHCID 24477—
反応物Hydrogen peroxide waterHCID 449047—
反応物Sodium BicarbonateHCID 516892—
反応物HCID 178438693HCID 178438693—
溶媒ChloroformHCID 6212—
生成物HCID 178438695HCID 17843869523%

反応条件

温度60 °C

反応手順

To a mixture of 4′-{[4-(trans-3-acetylcyclobutyl)-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile (1.3 g), 30% hydrogen peroxide water (3.5 g) and chloroform (20 mL) was gradually added trifluoroacetic acid anhydride (7.7 mL) at room temperature, and the reaction mixture was warmed to 60° C. and stirred for 24 hr. Saturated aqueous sodium hydrogen carbonate and sodium thiosulfate were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was dissolved in tetrahydrofuran (10 mL) and methanol (10 mL), 1N aqueous sodium hydroxide solution (5 mL) was added, and the mixture was stirred at room temperature for 30 min. 1N Aqueous hydrochloric acid solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.28 g, 23%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115136B2
出典データセットuspto-grants-2015_08
ORD IDord-e6a2c9044d7d4280a18eea17b3edafd2
出典メモuspto-grants-2015_08