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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596313Generated: November 4, 2026

3,5-Bis(trifluoromethyl)benzyl bromide → 2''-Methyl-5-(4-methyl-piperazin-1-yl)-biphenyl-2-carboxylic acid (3,5-bis-trifluoromethyl-benzyl)-methyl-amide

https://huagongshe.com/reaction/1596313

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant2-Methyl-5-(4-methyl-piperazin-1-yl)-biphenyl-2-carboxylic acid methylamideHCID 86757395—
SolventTetrahydrofuranHCID 8028—
Product2''-Methyl-5-(4-methyl-piperazin-1-yl)-biphenyl-2-carboxylic acid (3,5-bis-trifluoromethyl-benzyl)-methyl-amideHCID 987224929%

Reaction Steps

To a solution of 50 mg (0.15 mmol)2-methyl-5-(4-methyl-piperazin-1-yl)-biphenyl-2-carboxylic acid methylamide in 2 ml THF 0.2 ml of a 1 M solution (0.2 mmol) of potassium hexamethyldisilazide in THF was added at 0°. After 20 min. 0.028 ml (0.15 mmol) 3,5-bis(trifluoromethyl)benzyl bromide was added dropwise to the resulting suspension. The reaction was quenched with water after 1.5 h. The mixture was diluted with 5 ml 2 N NaOH solution and extracted with 3 5-ml portions of ethyl acetate. The combined organic extracts were dried (Na2SO4) and evaporated. Chromatography (SiO2, CH2Cl2/methanol 19:1) gave 25 mg (29%) 2′-Methyl-5-(4-methyl-piperazin-1-yl)-biphenyl-2-carboxylic acid (3,5-bis-trifluoromethyl-benzyl)-methyl-amide, MS (ISP): 550.5(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291465B1
Source datasetuspto-grants-2001_09
ORD IDord-98235728f3c847d1aa55524c5b91ee20
Source noteuspto-grants-2001_09