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HRID 379371作成日:2026年10月27日

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

https://huagongshe.com/reaction/379371

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物N-methyl-6-(4-methyl-piperazin-1-yl)-4-o-tolyl-nicotinamideHCID 15481065—
溶媒TetrahydrofuranHCID 8028—
生成物ImnopitantHCID 980851875%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06297375B1
出典データセットuspto-grants-2001_10
ORD IDord-38fccca7a56d478895a5615cd8e105d4
出典メモuspto-grants-2001_10