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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172451Generated: October 27, 2026

tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(3-bromo-2-fluorobenzoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1172451

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Bromo-2-fluorobenzoic acidHCID 2736313—
ReactantHCID 178526939HCID 178526939—
SolventChloroformHCID 6212—
ProductTert-butyl 4-(3-bromo-2-fluorobenzoyl)piperazine-1-carboxylateHCID 57562603—

Reaction Steps

To a mixture of 220 mg of 3-bromo-2-fluorobenzoic acid, 199 mg of tert-butyl piperazine-1-carboxylate and 5.0 ml of chloroform was added 171 mg of hydroxybenzotriazole monohydrate and 215 mg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride under cooling with ice, successively. After stirring at room temperature for 4 hours, saturated sodium bicarbonate was added to the reaction mixture, and the resulting mixture was extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated. The residue was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate=9/1 to 1/1) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834018B2
Source datasetuspto-grants-2010_11
ORD IDord-03f61db20e614ebb840834063fd3cccd
Source noteuspto-grants-2010_11