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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957930Generated: October 27, 2026

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

https://huagongshe.com/reaction/1957930

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 atmosphere of argon, 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 saturated sodium chloride solution and dried over sodium sulphate and the solvent is removed under reduced pressure. The residue is purified by flash chromatography (cyclohexane/ethyl acetate 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410090B2
Source datasetuspto-grants-2013_04
ORD IDord-051c2c558d91453bb59eca4f5883e70a
Source noteuspto-grants-2013_04