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HRID 452594作成日:2026年10月25日

Oxalyl chloride → N'-[3-[3-(trifluoromethyl)phenyl]propionyl]-1H-indazole-5-carbohydrazide

https://huagongshe.com/reaction/452594

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物Sodium BicarbonateHCID 516892—
反応物3-(3-Trifluoromethylphenyl)propanoic acidHCID 2777683—
反応物1H-Indazole-5-carbohydrazideHCID 43348973—
触媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物N'-[3-[3-(trifluoromethyl)phenyl]propionyl]-1H-indazole-5-carbohydrazideHCID 6866367751%

反応手順

To a solution of 3-[3-(trifluoromethyl)phenyl]propionic acid (437 mg, 2.00 mmol) and N,N-dimethylformamide (1 drop) in tetrahydrofuran (4 mL) was added oxalyl chloride (0.183 mL, 2.10 mmol) at room temperature, and the resulting mixture was stirred for 30 min. The reaction mixture was added dropwise to a mixture of 1H-indazole-5-carbohydrazide (352 mg, 2.00 mmol), tetrahydrofuran (10 mL) and saturated aqueous sodium hydrogen carbonate solution (10 mL) at room temperature, and the resulting mixture was stirred for 2 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from hexane/ethanol to give the title compound (383 mg, yield 51%) as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08492378B2
出典データセットuspto-grants-2013_07
ORD IDord-69f4f92427c74619a90092a49b028bc5
出典メモuspto-grants-2013_07