Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 415444생성일: 2026년 10월 24일
4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidine → N-(3-methoxy-1H-pyrazol-5-yl)-2-(methylthio)-6-(trifluoromethyl)pyrimidin-4-amine
https://huagongshe.com/ko/reaction/415444
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidine | HCID 248063 | — |
| 반응물 | HCID 178493289 | HCID 178493289 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | N-(3-methoxy-1H-pyrazol-5-yl)-2-(methylthio)-6-(trifluoromethyl)pyrimidin-4-amine | HCID 66624545 | 21.5% |
반응 단계
To a solution of 4-chloro-2-(methylthio)-6-(trifluoromethyl)pyrimidine (2.29 g) in absolute ethanol (50 mL) was added DIEPA (4.4 mL) and 5-methoxy-1H-pyrazol-3-amine hydrogen chloride salt (1.46 g). The resulting solution was heated at 90° C. for over night. The solvent was evaporated under reduced pressure. The crude compound was purified by Gilson (10-60% MeCN/H2O, 15 minutes) to give N-(3-methoxy-1H-pyrazol-5-yl)-2-(methylthio)-6-(trifluoromethyl)pyrimidin-4-amine as solid (0.64 g). m/z 306. N-(3-methoxy-1H-pyrazol-5-yl)-2-(methylthio)-6-(trifluoromethyl)pyrimidin-4-amine (240 mg) was dissolved in methylene chloride (5 mL), MCPBA (529 mg) was added. The resulting solution was stirred at room temperature for 0.5 hours and separate between methylene chloride and saturated sodium carbonate water solution. The organic layer was dried and solvent was removed under reduced pressure and low temperature. The crude product (270 mg) was carried on to do next step without further purification. m/z 338.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08088784B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-a3834143e34d4281a1cb9762b51be000 |
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| 출처 메모 | uspto-grants-2012_01 |
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