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HRID 570129作成日:2026年10月26日

Potassium Carbonate → 6-(4-Fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazole

https://huagongshe.com/reaction/570129

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2,3-Butanediol, dimethanesulfonateHCID 99909—
反応物3-(4-fluorophenyl)-1H-pyrazol-5-olHCID 178515624—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物6-(4-Fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazoleHCID 8948831271.8%

反応条件

温度60 °C

反応手順

To a solution of 3-(4-fluorophenyl)-1H-pyrazol-5-ol (3 g, 16.8 mmol) in DMF (15 mL) was added K2CO3 (9.3 g, 67.4 mmol) and butane-2,3-diyl dimethanesulfonate (4.8 g, 18.5 mmol) (prepared as described in US2010/41748) at room temperature and then stirred for 16 h at 60° C. Thereafter, the reaction mixture was diluted with cold water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulphate and concentrated to get the crude product. Purification by column chromatography over silica gel (eluent 5-10% ethyl acetate in petrol ether) yielded 6-(4-fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazole (2.8 g, 71%) as yellow oil and a mixture of diastereoisomers.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09023844B2
出典データセットuspto-grants-2015_05
ORD IDord-5fdc646e557142ff9c0d88ee8192ca33
出典メモuspto-grants-2015_05