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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074075Generated: October 27, 2026

tert-Butyl piperazine-1-carboxylate → tert-Butyl 4-(5-methylpyridin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2074075

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantBinap, (A+-)-HCID 634876—
Reactant5-Chloro-2-methylpyridineHCID 2762869—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Producttert-Butyl 4-(5-methylpyridin-2-yl)piperazine-1-carboxylateHCID 45788994—

Reaction Conditions

Temperature70 °C

Reaction Steps

Under an argon atmosphere, 2.50 g (19.6 mmol) of 2-methyl-5-chloropyridine and 4.38 g (23.5 mmol) of N-(tert-butyloxycarbonyl)piperazine are dissolved in 50 ml of absolute toluene. 2.26 g (23.5 mmol) of sodium tert-butoxide, 0.37 g (0.59 mmol) of BINAP and 0.36 g (0.39 mmol) of tris(dibenzylideneacetone)dipalladium are then added, and the mixture is heated at 70° C. for 12 h. After cooling, diethyl ether is added to the reaction mixture, the mixture is washed three times with a saturated sodium chloride solution and dried over sodium sulfate and the solvent is removed in vacuo. The residue is purified by flash chromatography (cyclohexane/ethyl acetate 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919489B2
Source datasetuspto-grants-2011_04
ORD IDord-8ef16fb1b63747939cc2eae8138a3910
Source noteuspto-grants-2011_04