Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878618Generated: October 31, 2026

1-Methylpiperazine → 1-(5-Bromopyridin-3-yl)-4-methylpiperazine

https://huagongshe.com/reaction/1878618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant3,5-DibromopyridineHCID 69369—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product1-(5-Bromopyridin-3-yl)-4-methylpiperazineHCID 53485314—

Reaction Steps

To a solution of 3,5-dibromopyridine (Sigma-Aldrich, St. Louis, USA) (1 eq, 8.4 mmol, 2.0 g) and 1-methylpiperazine (Sigma-Aldrich, St. Louis, USA) (1 eq, 8.4 mmol, 0.94 ml) in toluene (20 ml), Pd2(dba)3 (0.02 eq, 0.167 mmol, 153 mg), Xantphos (0.06 eq, 0.50 mmol, 290 mg), and NaOtBu (1.5 eq, 12.5 mmol, 1.2 g) are added. The resulting mixture is heated using microwave radiation at 120° C. for 15 min. The solvents are evaporated and aqueous HCl solution (1 M) is added. The aqueous layer is washed with DCM, adjusted to pH 10, and extracted with DCM. The organic layer is dried, filtered, and concentrated to give the title compound, [M+H]+=257.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314112B2
Source datasetuspto-grants-2012_11
ORD IDord-d0234e594aaa4d9988e06d176707d95b
Source noteuspto-grants-2012_11