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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 854551생성일: 2026년 10월 26일

Thiophenol → (5-Methyl-2-(6-phenylsulfanyl-pyridin-3-yl)-oxazol-4-yl]-acetic acid methyl ester

https://huagongshe.com/reaction/854551

반응식

참여 물질

역할이름HCID투입량
반응물ThiophenolHCID 7969—
반응물Cesium carbonateHCID 10796—
반응물[2-(6-Chloro-pyridin-3-yl)-5-methyl-oxazol-4-yl]-acetic acid methyl esterHCID 58765666—
용매DimethylformamideHCID 6228—
생성물(5-Methyl-2-(6-phenylsulfanyl-pyridin-3-yl)-oxazol-4-yl]-acetic acid methyl esterHCID 5876578974%

반응 단계

[2-(6-Chloro-pyridin-3-yl)-5-methyl-oxazol-4-yl]-acetic acid methyl ester (4.8 g, 17.98 mmol) is dissolved in anhydrous dimethylformamide (100 mL) and allowed to stir under nitrogen. Benzenethiol (2.78 mL, 27 mmol) is added by syringe, followed by anhydrous cesium carbonate (12.6 g, 36 mmol). The mixture is allowed to stir under nitrogen 50° C. and monitored by HPLC. After complete consumption of strating material, the solution is quenched with 1N sodium hydroxide solution, diluted with ethyl acetate, and then enough water added to dissolve the solids. The two phases are separated and the organic layer is washed with water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The pure [5-Methyl-2-(6-phenylsulfanyl-pyridin-3-yl)-oxazol-4-yl]-acetic acid methyl ester (4.51 g, 13.2 mmol) is isolated in 74% yield after column chromatography.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259175B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-29b16ac75d894c30bc6d6640075e7bc4
출처 메모uspto-grants-2007_08