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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160117Generated: October 27, 2026

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

https://huagongshe.com/reaction/1160117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenamine, 3-bromo-4-methyl-HCID 82187—
ReactantMethyl 4-((4-methylpiperazin-1-yl)methyl)benzoateHCID 782222—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
ProductN-(3-bromo-4-methyl-phenyl)4-(4-methyl-piperazin-1-ylmethyl)-benzamideHCID 10309714—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816359B2
Source datasetuspto-grants-2010_10
ORD IDord-5e8608130bf9465c827b32fb614d70af
Source noteuspto-grants-2010_10