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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 925268생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/925268

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Methyl 3-chloroisonicotinateHCID 15324397—
반응물3,3-Difluoro-3-(4-fluorophenyl)-propane-1-thiolHCID 86720162—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-[[3,3-Difluoro-3-(4-fluorophenyl)-propyl]sulfanyl]-pyridine-4-carboxylic acid methyl esterHCID 8672016534%

반응 조건

온도90 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09284286B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-b879061a85c447d7833a3fb4f337e5e4
출처 메모uspto-grants-2016_03