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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017431Generated: October 25, 2026

3,5-Bis(trifluoromethyl)benzyl bromide → Imnopitant

https://huagongshe.com/reaction/1017431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantN-methyl-6-(4-methyl-piperazin-1-yl)-4-o-tolyl-nicotinamideHCID 15481065—
SolventTetrahydrofuranHCID 8028—
ProductImnopitantHCID 980851875%

Reaction Steps

To a solution of 750 mg (2.32 mmol) N-methyl-6-(4-methyl-piperazin-1-yl)-4-o-tolyl-nicotinamide in 16 ml tetrahydrofuran, 3 ml of a 1 M solution (3 mmol) of potassium hexamethyldisilazide in tetrahydrofuran was added at room temperature. After 1 h, 0.43 ml (2.3 mmol) 3,5-bis(trifluoromethyl)benzyl bromide was added dropwise to the resulting suspension. The reaction was quenched with water after 1 h and the mixture was extracted with three 20 ml portions of ethyl acetate. The combined organic extracts were washed with saturated aqueous sodium chloride solution, dried with sodium sulfate and concentrated. Column chromatography gave 950 mg (74%) N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-6-(4-methyl-piperazin-1-yl)-4-o-tolyl-nicotinamide. The white foam was dissolved in a small amount of diethyl ether and treated with 2 ml 3 N hydrochloric acid solution in diethyl ether. Concentration afforded 1.02 g (74%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479483B2
Source datasetuspto-grants-2002_11
ORD IDord-f3a703314626422f9f21e7556ec249e7
Source noteuspto-grants-2002_11