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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1401920생성일: 2026년 10월 26일

Ammonia → 2,5-difluoro-4-[2-pyridazin-4-yl-4-(trifluoromethyl)phenoxy]-N-1,2,4-thiadiazol-5-ylbenzenesulfonamide

https://huagongshe.com/reaction/1401920

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Hydrochloric AcidHCID 313—
반응물Trifluoroacetic acidHCID 6422—
반응물Potassium CarbonateHCID 11430—
반응물N-(2,4-Dimethoxybenzyl)-2,4,5-trifluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamideHCID 59436583—
반응물2-(Pyridazin-4-yl)-4-(trifluoromethyl)phenolHCID 135741697—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2,5-difluoro-4-[2-pyridazin-4-yl-4-(trifluoromethyl)phenoxy]-N-1,2,4-thiadiazol-5-ylbenzenesulfonamideHCID 46841351—

반응 단계

The mixture of N-(2,4-dimethoxybenzyl)-2,4,5-trifluoro-N-1,2,4-thiadiazol-5-ylbenzenesulfonamide (Preparation 647, 44 mg, 0.10 mmol), 2-pyridazin-4-yl-4-(trifluoromethyl)phenol (Preparation 712, 34 mg, 0.10 mmol), and potassium carbonate (55 mg, 0.40 mmol) in N,N-dimethylformamide (1.0 ml) was stirred at room temperature for 24 hours. The reaction mixture was poured into aqueous 2 M hydrochloric acid solution (5.0 ml) and filtered to give a solid. The solid was dissolved in dichloromethane (1.0 ml) and trifluoroacetic acid (1.0 ml) was added to the solution. The resulting solution was stirred for 16 hours. Methanol (5.0 ml) was added to the reaction mixture and filtered off polymeric solid. The filtrate was concentrated in vacuo to give a residue. The residue was passed through a 5 g SCX™ column with 1:1 dichloromethane:methanol solution and then 1:0.75:0.25 dichloromethane:methanol:7N ammonia solution in methanol. The filtrate was concentrated in vacuo and purified by HPLC. Yield 7.3 mg, 14%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08907101B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-c9d42bb62e8f4653ac22a044c8893d4a
출처 메모uspto-grants-2014_12