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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

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물3-Amino-5-(trifluoromethyl)-1,2-dihydropyridin-2-oneHCID 2315787—
반응물3-Chloroisonicotinoyl chlorideHCID 20487499—
용매WaterHCID 962—
생성물3-chloro-N-[2-hydroxy-5-(trifluoromethyl)pyridin-3-yl]isonicotinamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08242133B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-a26a670b9b8f4bbf92222ed11f4f3d87
출처 메모uspto-grants-2012_08