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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1017431Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1017431

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
EduktN-methyl-6-(4-methyl-piperazin-1-yl)-4-o-tolyl-nicotinamideHCID 15481065—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktImnopitantHCID 980851875%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06479483B2
Quelldatensatzuspto-grants-2002_11
ORD IDord-f3a703314626422f9f21e7556ec249e7
Quellennotizuspto-grants-2002_11