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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324738생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/324738

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methyl 4-chloro-3-nitrobenzoateHCID 735797—
반응물1-[4-(3-Aminophenyl)piperazin-1-yl]ethan-1-oneHCID 11117539—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물Methyl 4-(3-(1-acetylpiperazin-4-yl)anilino)-3-nitrobenzoateHCID 2274190585%

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06218547B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-33d64f71547541ccbe2ea65f43ebf04b
출처 메모uspto-grants-2001_04