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HRID 57795作成日:2026年10月24日

Triethylamine → 5-nitro-1H-pyrazole-3-carboxylic acid [2-(4-chloro-phenyl)-ethyl]-amide

https://huagongshe.com/ja/reaction/57795

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物2-(4-Chlorophenyl)ethylamineHCID 67430—
反応物5-Nitro-1H-pyrazole-3-carboxylic acidHCID 86222684—
反応物HCID 178418300HCID 178418300—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物5-nitro-1H-pyrazole-3-carboxylic acid [2-(4-chloro-phenyl)-ethyl]-amideHCID 13634435443%

反応手順

To a solution of 5-nitro-1H-pyrazole-3-carboxylic acid (200 mg, 1.3 mmol, 1 eq) in tetrahydrofuran (5 mL) were added triethylamine (350 μL, 1.9 mmol, 1.5 eq), hydroxybenzotriazole (HOBT) (257 mg, 1.27 mmol, 1 eq), 2-(4-chloro-phenyl)-ethylamine (180 μL, 1.27 mmol, 1 eq) and EDCI (364 mg, 1.9 mmol, 1.5 eq). The mixture was stirred at room temperature during 20 h. Water (10 mL) was then added and the aqueous phase was extracted with ethyl acetate (2×15 mL). The organic layers were dried over magnesium sulfate, filtered and evaporated in vacuo. The crude residue was purified by flash chromatography using cyclohexane and ethyl acetate (100/0) to (50/50) to afford 5-nitro-1H-pyrazole-3-carboxylic acid [2-(4-chloro-phenyl)-ethyl]-amide as white solid (160 mg, 43% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434745B2
出典データセットuspto-grants-2016_09
ORD IDord-7a0f096c90634fb5b970bdaed8626bd8
出典メモuspto-grants-2016_09