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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403569Generated: October 26, 2026

tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2403569

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3-Bromo-2-methylpyridineHCID 1201003—
ReactantSodium tert-butoxideHCID 45051916—
SolventTolueneHCID 1140—
ProductTert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylateHCID 6810632798%

Reaction Conditions

Temperature100 °C

Reaction Steps

3-Bromo-2-methylpyridine (500 mg) and tert-butyl piperazine-1-carboxylate (650 mg) were dissolved in toluene (7.5 ml), and (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one_palladium (3:2) (40 mg), 1,1′-binaphthalene-2,2′-diylbis(diphenylphosphine) (18 mg), and 2-methylpropan-2-ol sodium (391 mg) were added thereto in this order under a nitrogen atmosphere, followed by warming to 100° C. and stirring overnight. The reaction mixture was subjected to liquid separation with CHCl3 and water, the organic layer was dried over Na2SO4, and then the solvent was evaporated. The obtained residue was purified by silica gel column chromatography (CHCl3 to 5% MeOH/CHCl3) to obtain tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylate (790 mg) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802679B2
Source datasetuspto-grants-2014_08
ORD IDord-98cadd563f1c443daa2dfa7faf16755c
Source noteuspto-grants-2014_08