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HRID 324738作成日:2026年10月26日

Triethylamine → Methyl 4-(3-(1-acetylpiperazin-4-yl)anilino)-3-nitrobenzoate

https://huagongshe.com/reaction/324738

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methyl 4-chloro-3-nitrobenzoateHCID 735797—
反応物1-[4-(3-Aminophenyl)piperazin-1-yl]ethan-1-oneHCID 11117539—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物Methyl 4-(3-(1-acetylpiperazin-4-yl)anilino)-3-nitrobenzoateHCID 2274190585%

反応条件

温度80 °C

反応手順

To a solution of methyl 4-chloro-3-nitrobenzoate (2.0 g, 9.28 mmol) in anhydrous NMP (5 ml) was added 2d (2.03 g, 9.28 mmol) and triethylamine (1.3 ml, 9.28 mmol). The mixture was heated with stirring to 80° C. overnight. The cooled solution was poured into ice-water (50 ml) and the resulting mixture was extracted with ethyl acetate (3×10 ml). The combined organic extracts were washed with water, dried over sodium sulfate and evaporated to dryness. The residue was triturated with petroleum ether to yield methyl 4-(3-(1-acetylpiperazin-4-yl)anilino)-3-nitrobenzoate (3.14 g, 85%) as red crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06218547B1
出典データセットuspto-grants-2001_04
ORD IDord-33d64f71547541ccbe2ea65f43ebf04b
出典メモuspto-grants-2001_04