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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21119생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/21119

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물1-MethylpiperazineHCID 53167—
반응물3,4-Diaminobenzoic acidHCID 69263—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물(3,4-Diaminophenyl)(4-methylpiperazin-1-yl)methanoneHCID 2991969118%

반응 조건

온도0 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7c9f628c125a4b0fa7dd23f26f63f52c
출처 메모uspto-grants-2010_06