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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358081Generated: October 26, 2026

Sodium Hydroxide → 4-{5-[(3,5-Bis-trifluoromethyl-benzyl)-methyl-carbamoyl]-4-o-tolyl-pyridin-2-yl}-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1358081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant4-(5-Methylcarbamoyl-4-o-tolyl-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 54387824—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-{5-[(3,5-Bis-trifluoromethyl-benzyl)-methyl-carbamoyl]-4-o-tolyl-pyridin-2-yl}-piperazine-1-carboxylic acid tert-butyl esterHCID 985231970.8%

Reaction Steps

To a solution of 6.28 g (15.3 mmol) 4-(5-methylcarbamoyl-4-o-tolyl-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester in 250 ml tetrahydrofuran 20 ml of a 1 M solution (20 mmol) of potassium hexamethyldisilazide in tetrahydrofuran were added at 0° C. After 30 min, 2.81 ml (15.3 mmol) 3,5-bis(trifluoromethyl)benzyl bromide were added dropwise. The reaction mixture was allowed to warm to room temperature over night. Addition of water and 1 M aqueous sodium hydroxide solution was followed by extraction with three portions of ethyl acetate. The combined organic extracts were dried with sodium sulfate and concentrated. Flash column chromatography gave 6.89 g (70.8%) of the parent compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593472B2
Source datasetuspto-grants-2003_07
ORD IDord-710dc97e390c408eaac05121ecbaf239
Source noteuspto-grants-2003_07