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HRID 1474473作成日:2026年10月25日

Acetic Anhydride → 4-((5-Fluoro-3-pyridinyl)methylene)-2-(2-thienyl)-5(4H)-oxazolone

https://huagongshe.com/reaction/1474473

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物Sodium AcetateHCID 517045—
反応物((2-Thienylcarbonyl)amino)acetic acidHCID 679227—
反応物5-Fluoropyridine-3-carbaldehydeHCID 14141159—
溶媒WaterHCID 962—
生成物4-((5-Fluoro-3-pyridinyl)methylene)-2-(2-thienyl)-5(4H)-oxazoloneHCID 7523840968.1%

反応条件

温度90 °C

反応手順

To a screw-capped test tube, N-(2-thienylcarbonyl)glycine (56 mg, 0.3 mmol), 5-fluoro-3-pyridinecarboxaldehyde (41 mg, 0.3 mmol), sodium acetate (25 mg, 0.3 mmol) and acetic anhydride (0.3 mL) were added. The test tube was sealed, and it was then stirred at an external temperature of 90° C. Three hours later, the temperature of the reaction solution was returned to room temperature, and water (1.5 mL) was then added thereto. The obtained mixture was stirred at the same temperature as described above for 1.5 hours. Thereafter, the precipitated crystal was collected by filtration, and it was washed with water (5 mL) and was then dried under reduced pressure, so as to obtain 56 mg of the above-captioned compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09018238B2
出典データセットuspto-grants-2015_04
ORD IDord-fae00b65beba4bc18770bfcd40ef8c5d
出典メモuspto-grants-2015_04