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HRID 8479作成日:2026年10月24日

Water → (S)-Diethyl (7,8-Difluoro-3-Methyl-3,4-Dihydro-2H-[1,4]Benzoxazin-4-Yl)Methylene-Malonate

https://huagongshe.com/ja/reaction/8479

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Diethyl (ethoxymethylene)malonateHCID 6871—
反応物Potassium HydroxideHCID 14797—
反応物(2S)-2-(2,3,4-Trifluoroanilino)propanolHCID 11401466—
触媒Tetrahexylammonium chlorideHCID 80021—
溶媒DimethylformamideHCID 6228—
生成物(S)-Diethyl (7,8-Difluoro-3-Methyl-3,4-Dihydro-2H-[1,4]Benzoxazin-4-Yl)Methylene-MalonateHCID 11089557—

反応条件

温度60 °C

反応手順

At room temperature, KOH (330 mg) and tetrahexylammonium chloride (190.1 mg) were dissolved in DMF (15 ml). After adding a solution (5 ml) of (2S)-2-(2,3,4-trifluoroanilino)propanol (1 g, 99.8% ee) and diethyl ethoxymethylenemalonate (2.09 g) in DMF, the mixture was stirred for 1 hour. Next, it was heated to 60° C. and a solution (5 ml) of KOH (330 mg) and diethyl ethoxymethylenemalonate (120 mg) in DMF was added thereto. The resultant mixture was stirred at the same temperature for 5 hours. After adding water, the liquid reaction mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. After evaporating the solvent, the obtained residue was subjected to silica gel column chromatography. Thus, 1.37 g (99.8% ee) of the title compound was obtained as a yellow oily substance. Various spectral data was identical with those described in Japanese Patent No. 2,769,174.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087778B2
出典データセットuspto-grants-2006_08
ORD IDord-ffa02a76540e496189594119513487f8
出典メモuspto-grants-2006_08