Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 884987생성일: 2026년 10월 26일
Dimethylformamide → 3-chloro-N-[2-hydroxy-5-(trifluoromethyl)pyridin-3-yl]isonicotinamide
https://huagongshe.com/reaction/884987
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 3-Amino-5-(trifluoromethyl)-1,2-dihydropyridin-2-one | HCID 2315787 | — |
| 반응물 | 3-Chloroisonicotinoyl chloride | HCID 20487499 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 3-chloro-N-[2-hydroxy-5-(trifluoromethyl)pyridin-3-yl]isonicotinamide | HCID 178522159 | — |
반응 단계
A mixture of 0.88 g of 3-chloroisonicotinic acid, 5 ml of thionyl chloride and 20 mg of DMF was heated to reflux for three hours. After the reaction mixture was cooled to room temperature, it was concentrated under reduced pressure to give 3-chloroisonicotinic acid chloride. The resultant 3-chloroisonicotinic acid chloride and 4 ml of DMF was added dropwise to a mixture of 1.0 g of 3-amino-2-hydroxy-5-trifluoromethylpyridine, 1.14 g of triethylamine and 8 ml of DMF while ice-cooling. The reaction mixture was stirred at room temperature for one hour, and then stirred while heating at 50° C. for 30 minutes. The reaction mixture was cooled to room temperature, and then water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with water and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.87 g of 3-chloro-N-[2-hydroxy-5-(trifluoromethyl)pyridin-3-yl]isonicotinamide.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08242133B2 |
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| 출처 데이터셋 | uspto-grants-2012_08 |
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| ORD ID | ord-a26a670b9b8f4bbf92222ed11f4f3d87 |
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| 출처 메모 | uspto-grants-2012_08 |
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