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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352830Generated: October 30, 2026

Sodium Chloride → 4-(tert-Butoxycarbonyl)-2,2-dimethyl-1-[4-(pyridin-4-yl)benzoyl]piperazine

https://huagongshe.com/reaction/352830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant1-Boc-3,3-dimethylpiperazineHCID 22710387—
Reactant4-(4-Pyridyl)benzoateHCID 22711144—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product4-(tert-Butoxycarbonyl)-2,2-dimethyl-1-[4-(pyridin-4-yl)benzoyl]piperazineHCID 22710764—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1-(tert-butoxycarbonyl)-3,3-dimethylpiperazine (173 mg) in a mixture of N,N-dimethylformamide (2.5 ml) and triethylamine (1.0 ml) was added (4-nirophenyl) 4-(4-pyridyl)benzoate (330 mg). The resulting mixture was stirred at 60° C. for 5 days. The reaction mixture was diluted with methylene chloride and then added with a saturated aqueous solution of sodium chloride to form two layers. The organic layer obtained by separation was washed with a saturated aqueous solution of sodium bicarbonate and an aqueous solution of sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crudely purified product was purified by chromatography on a silica gel column (methylene chloride:methanol=50:1), whereby the title compound (199 mg) was obtained as colorless amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747023B1
Source datasetuspto-grants-2004_06
ORD IDord-275e5b49534645a393c00e5c79668fb3
Source noteuspto-grants-2004_06