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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273289생성일: 2026년 10월 25일

Benzenamine, 3-bromo-4-methyl- → N-(3-bromo-4-methyl-phenyl)4-(4-methyl-piperazin-1-ylmethyl)-benzamide

https://huagongshe.com/reaction/273289

반응식

참여 물질

역할이름HCID투입량
반응물Benzenamine, 3-bromo-4-methyl-HCID 82187—
반응물Methyl 4-((4-methylpiperazin-1-yl)methyl)benzoateHCID 782222—
반응물TrimethylaluminumHCID 16682925—
용매TolueneHCID 1140—
생성물N-(3-bromo-4-methyl-phenyl)4-(4-methyl-piperazin-1-ylmethyl)-benzamideHCID 10309714—

반응 조건

온도0 °C

반응 단계

A solution of trimethylaluminium (2M in toluene, 15.0 ml) is added over a period of 30 min to a solution of 3-bromo-4-methyl-aniline(2.15 g, 11.5 mmol) and 4-(4-methyl-piperazin-1-ylmethyl)-benzoic acid methyl ester (2.87 g, 11.5 mmol) in toluene (20 ml) at 40° C. under an atmosphere of argon. After gas evolution ceases, the reaction mixture is stirred 30 min before being cooled to 0° C. and partitioned between cold aqueous 1N NaOH (100 ml) and toluene (100 ml). The organic layer is extracted with aqueous saturated NH4Cl (100 ml) and aqueous saturated NaCl (100 ml) The organic layer is concentrated in vacuo to give 4.69 g (97 area % by HPLC) of the title compound as pale yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456283B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-a96d00eed30545c5bcbe3c64f9b42c98
출처 메모uspto-grants-2008_11