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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273289Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/273289

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenamine, 3-bromo-4-methyl-HCID 82187—
EduktMethyl 4-((4-methylpiperazin-1-yl)methyl)benzoateHCID 782222—
EduktTrimethylaluminumHCID 16682925—
LösungsmittelTolueneHCID 1140—
ProduktN-(3-bromo-4-methyl-phenyl)4-(4-methyl-piperazin-1-ylmethyl)-benzamideHCID 10309714—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456283B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-a96d00eed30545c5bcbe3c64f9b42c98
Quellennotizuspto-grants-2008_11