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HRID 21119作成日:2026年10月26日

Triethylamine → (3,4-Diaminophenyl)(4-methylpiperazin-1-yl)methanone

https://huagongshe.com/reaction/21119

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl chloroformateHCID 10928—
反応物1-MethylpiperazineHCID 53167—
反応物3,4-Diaminobenzoic acidHCID 69263—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物(3,4-Diaminophenyl)(4-methylpiperazin-1-yl)methanoneHCID 2991969118%

反応条件

温度0 °C

反応手順

HOBT monohydrate (2.00 g, 13.1 mmol) was dissolved in DMF (20 mL), and the solution was added with triethylamine (2.54 mL, 18.2 mmol) and ethylchloroformate (1.24 mL, 13.0 mmol), followed by stirring at 0° C. for 3 hours. Then, the mixture was added with triethylamine (4.22 mL, 30.3 mmol) and 3,4-diaminobenzoic acid (1.86 g, 12.2 mmol), followed by stirring at the same temperature for 2 hours. The mixture was added with a solution of N-methylpiperazine (1.21 mL, 10.9 mmol) in DMF (20 mL), followed by further stirring for 30 minutes. The reaction mixture was added with water (2 mL) and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol/7 mol/L ammonia-methanol solution=50/0.5/0.5-7/0.5/0.5) and preparative thin-layer chromatography (chloroform/methanol/7 mol/L ammonia-methanol solution=4/0.5/0.5) to obtain (3,4-diaminophenyl)(4-methylpiperazin-1-yl)methanone (455 mg, yield 18%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745641B2
出典データセットuspto-grants-2010_06
ORD IDord-7c9f628c125a4b0fa7dd23f26f63f52c
出典メモuspto-grants-2010_06