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HRID 46253作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/46253

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Hydrochloric AcidHCID 313—
反応物Trifluoroacetic acidHCID 6422—
反応物Potassium CarbonateHCID 11430—
反応物N-(2,4-Dimethoxybenzyl)-2,4,5-trifluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamideHCID 59436583—
反応物2-(Pyridazin-4-yl)-4-(trifluoromethyl)phenolHCID 135741697—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物2,5-difluoro-4-[2-pyridazin-4-yl-4-(trifluoromethyl)phenoxy]-N-1,2,4-thiadiazol-5-ylbenzenesulfonamideHCID 46841351—

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541588B2
出典データセットuspto-grants-2013_09
ORD IDord-8daee7a4864144e99b62da57688e9470
出典メモuspto-grants-2013_09