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HRID 2354763作成日:2026年10月25日

Water → N-(2-cyclopropyl-2-hydroxyethyl)-6-(4-(2-(trifluoromethyl)benzoyl)piperazin-1-yl)pyridazine-3-carboxamide

https://huagongshe.com/reaction/2354763

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物1-[2-(Trifluoromethyl)benzoyl]piperazineHCID 16733784—
反応物6-CHLOROPYRIDAZINE-3-CARBOXYLIC Acid (2-CYCLOPROPYL-2-HYDROXYETHYL)AMIDEHCID 63296384—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒DimethylformamideHCID 6228—
生成物N-(2-cyclopropyl-2-hydroxyethyl)-6-(4-(2-(trifluoromethyl)benzoyl)piperazin-1-yl)pyridazine-3-carboxamideHCID 1175159932%

反応条件

温度80 °C

反応手順

To a solution of 6-chloropyridazine-3-carboxylic acid (2-cyclopropyl-2-hydroxyethyl)amide (58 mg, 0.24 mmol) in 10 mL of DMF was added 1,8-diazabicylco[5.4.0]undec-7-ene (0.109 g), piperazin-1-yl-(2-trifluoromethylphenyl)methanone (86.7 mg, 0.33 mmol) and Bu4NI (4 mg, 0.01 mmol). The mixture was heated at 80° C. overnight. Water was added and the mixture was extracted with ethyl acetate (2×15 mL). The organic extract was washed with diluted HCl, followed by bicarbonate solution and brine, then dried over Na2SO4 and concentrated. The residue was dissolved in small amount of dichloromethane and purified by column chromatography eluted with ethyl acetate to yield the product as a white solid (35.5 mg, 32% yield). 1H NMR (300 MHz, CDCl3) δ 8.24, 8.02, 7.73, 7.58, 7.34, 6.98, 4.04, 3.85, 3.52, 3.33, 3.10, 2.60-2.41, 0.95, 0.52, 0.32. MS (ES+) m/z 464.3 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07754711B2
出典データセットuspto-grants-2010_07
ORD IDord-100eb7bcaa5b40c992fd7155b79fe0f5
出典メモuspto-grants-2010_07