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HRID 133725作成日:2026年10月27日

Acetic Acid → {1-(4-Fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-oxoazetidin-2-yl}-benzonitrile

https://huagongshe.com/reaction/133725

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物BistrimethylsilylacetamidHCID 11708267—
反応物Tetrabutylammonium Fluoride TrihydrateHCID 11726816—
反応物4-[5-(4-Fluorophenyl)-1-(4-fluorophenylamino)-5-hydroxy-2-(2-oxo-4-phenyloxazolidine-3-carbonyl)-pentyl]-benzonitrileHCID 22252064—
溶媒tert-Butyl methyl etherHCID 15413—
生成物{1-(4-Fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-oxoazetidin-2-yl}-benzonitrileHCID 22252073—

反応条件

温度40 °C

反応手順

2 g of 4-[5-(4-Fluorophenyl)-1-(4-fluorophenylamino)-5-hydroxy-2-(2-oxo-4-phenyl-oxazolidine-3-carbonyl)-pentyl]-benzonitrile were dissolved in 20 ml of methyl-tert-butyl ether and, together with 100 mg of tetrabutylammonium fluoride trihydrate and 1.3 ml of bistrimethylsilyl acetamide, heated at 40° C. for about 1 h. The reaction was monitored by thin-layer chromatography. After the reaction ended, 0.2 ml of glacial acetic acid were initially added and the mixture was stirred for 30 min and then concentrated. 20 ml of a mixture of isopropanol/2N sulfuric acid=10:1 were added to the residue, and the mixture was stirred for 1 hour. Following addition of a spatula tip of solid sodium bicarbonate, the mixture was again concentrated under reduced pressure. The residue was taken up in ethyl acetate and the organic phase was washed with water and dried. The residue was, after removal of the solvent, purified by column chromatography (SiO2, CH2Cl2/methanol=100:1). This gave the product of molecular weight 418.45 (C25H20F2N2O2); MS (DCI+) 419 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390790B2
出典データセットuspto-grants-2008_06
ORD IDord-4ed0447e78444586b58761d51af3f404
出典メモuspto-grants-2008_06