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HRID 1480068作成日:2026年10月27日

Sodium hydride → 5-Chloro-4-(oxetan-3-yloxy)-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/1480068

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Oxetan-3-olHCID 9942117—
反応物5-Chloro-4-iodo-2-pyridinecarboxylic acidHCID 85592091—
溶媒DimethylformamideHCID 6228—
生成物5-Chloro-4-(oxetan-3-yloxy)-pyridine-2-carboxylic acidHCID 90203475111%

反応条件

温度120 °C

反応手順

To a solution of 5-chloro-4-iodo-pyridine-2-carboxylic acid (CAN 120643-06-3, 360 mg, 1.27 mmol) in DMF (10 mL) was added with stirring Oxetan-3-ol (CAN 7748-36-9, 104 mg, 1.4 mmol) and sodium hydride 60% (107 mg, 2.67 mmol). The resulting mixture was stirred at room temperature for 30 min and at 120° C. for 25 h, cooled and the reaction mixture was concentrated in vacuo. The residue was suspended with ethylacetate, transferred into a separatory funnel and extracted with 4.0 mL of 0.5M aqueous solution hydrochloric acid. The organic phase was collected and the aqueous phase was back-extracted with ethylacetate. The organic phases were combined, dried over sodium sulfate and evaporated down to dryness to give the title compound (323 mg, 111%) as a solid which was used crude without any further purification. MS (ESI, m/z): 228.4 (M−H+)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09409866B2
出典データセットuspto-grants-2016_08
ORD IDord-27090df4d3f247e4bf699d6a9f63829e
出典メモuspto-grants-2016_08