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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 387453생성일: 2026년 10월 27일

m-Hydroxybenzohydrazide → 3-[5-(4-Chloro-3-trifluoromethyl-phenylamino)-4h[1,2,4]triazol-3-yl]-phenol

https://huagongshe.com/reaction/387453

반응식

참여 물질

역할이름HCID투입량
반응물m-HydroxybenzohydrazideHCID 79889—
반응물1-[4-chloro-3-(trifluoromethyl)phenyl]-S-methylisothiourea hydroiodideHCID 178504001—
용매PyridineHCID 1049—
생성물3-[5-(4-Chloro-3-trifluoromethyl-phenylamino)-4h[1,2,4]triazol-3-yl]-phenolHCID 17851598931.3%

반응 단계

3-hydroxybenzoic acid hydrazide (2.98 g, 19.58 mmol) and S-methyl N-[4-chloro-3-(trifluoromethyl)phenyl]isothiourea hydroiodide (7.78 g, 19.63 mmol) were suspended in 40 mL of anhydrous pyridine. The reaction mixture was refluxed for 18 hours, during which time it changed color from yellow into dark-red. Then it was cooled down to ambient temperature and poured with stirring into 250 mL of ice-water. The aqueous solution was decanted and the oily residue was purified by silica gel chromatography on Isco column using 0=>50% gradient of ethyl acetate in hexane. Solvent was removed in vacuo to give the title product as a white solid (2.176 g). 31.3% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372971B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-854ec41e5fb84ca4ae891ea9a3bcaa1f
출처 메모uspto-grants-2013_02