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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Thiophenol | HCID 7969 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | [2-(6-Chloro-pyridin-3-yl)-5-methyl-oxazol-4-yl]-acetic acid methyl ester | HCID 58765666 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (5-Methyl-2-(6-phenylsulfanyl-pyridin-3-yl)-oxazol-4-yl]-acetic acid methyl ester | HCID 58765789 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07259175B2 |
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| 출처 데이터셋 | uspto-grants-2007_08 |
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| ORD ID | ord-29b16ac75d894c30bc6d6640075e7bc4 |
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| 출처 메모 | uspto-grants-2007_08 |
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