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HRID 17583作成日:2026年10月24日

Dimethyl malonate → Dimethyl 2-(4-cyano-2-cyclopropyl-5-methyl-6-phenyl-1,3-benzoxazol-7-yl)malonate

https://huagongshe.com/ja/reaction/17583

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl malonateHCID 7943—
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
反応物2-Cyclopropyl-7-fluoro-5-methyl-6-phenylbenzoxazole-4-carbonitrileHCID 51041428—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物Dimethyl 2-(4-cyano-2-cyclopropyl-5-methyl-6-phenyl-1,3-benzoxazol-7-yl)malonateHCID 8663088077.4%

反応条件

温度90 °C

反応手順

2-Cyclopropyl-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile (I-173) (2.69 g, 9.20 mmol) was dissolved in dimethyl sulfoxide (50 ml), then at room temperature, potassium carbonate (3.82 g, 27.61 mmol) and dimethyl malonate (2.1 ml, 18.41 mmol) were added. The solution was stirred under nitrogen atmosphere at 90° C. for 14 hours. The reaction liquid was cooled to room temperature, then ethyl acetate and water were added to the reaction liquid, followed by vigorously stirring for 10 minutes. The aqueous layer was separated, extracted twice with ethyl acetate. The organic layers were combined, washed with saturated brine, then dried over anhydrous sodium sulfate. The insoluble matter was separated by filtration, the solvent was evaporated away, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, n-hexane:ethyl acetate=3:1, v/v) to obtain the entitled compound (2.878 g, 77%) as a colorless gel

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737166B2
出典データセットuspto-grants-2010_06
ORD IDord-1a67ffd2cb4b413280569e617930fcf0
出典メモuspto-grants-2010_06