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HRID 925268作成日:2026年10月26日

Cesium carbonate → 3-[[3,3-Difluoro-3-(4-fluorophenyl)-propyl]sulfanyl]-pyridine-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/925268

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Methyl 3-chloroisonicotinateHCID 15324397—
反応物3,3-Difluoro-3-(4-fluorophenyl)-propane-1-thiolHCID 86720162—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-[[3,3-Difluoro-3-(4-fluorophenyl)-propyl]sulfanyl]-pyridine-4-carboxylic acid methyl esterHCID 8672016534%

反応条件

温度90 °C

反応手順

To a solution of 3-chloro-pyridine-4-carboxylic acid methyl ester (0.28 g, 1.65 mmol) in DMF (10 ml) are added cesium carbonate (2.68 g, 8.25 mmol) and 3,3-difluoro-3-(4-fluorophenyl)-propane-1-thiol (synthesized according to the methods described in sections a) and b) of example 3) (0.34 g, 1.65 mmol) in a sealed tube. The reaction mixture is stirred at 90° C. for 1 h. After completion of the reaction, the mixture is diluted with water (15 ml) and extracted with EtOAc (3×20 ml). The organic layer is washed with water (20 ml), brine (20 ml), dried over anhydrous sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 10% acetone/hexane) to yield 3-[[3,3-difluoro-3-(4-fluorophenyl)-propyl]sulfanyl]-pyridine-4-carboxylic acid methyl ester (0.19 g, 0.56 mmol, 34%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09284286B2
出典データセットuspto-grants-2016_03
ORD IDord-b879061a85c447d7833a3fb4f337e5e4
出典メモuspto-grants-2016_03