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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885950Generated: October 26, 2026

1-Methylpiperazine → 1-(2-Chloropyridin-4-YL)-4-methylpiperazine

https://huagongshe.com/reaction/885950

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant2-Chloro-4-iodopyridineHCID 1516511—
ReactantSodium t-butoxideHCID 23676156—
CatalystDichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II)HCID 53384307—
SolventTolueneHCID 1140—
Product1-(2-Chloropyridin-4-YL)-4-methylpiperazineHCID 7221889977%

Reaction Conditions

Temperature115 °C

Reaction Steps

To a mixture of 2-chloro-4-iodopyridine (300 mg, 1.24 mmol) in toluene (4 mL) was added 1-methylpiperazine (0.14 mL, 1.24 mmol), sodium tert-butoxide (239 mg, 2.44 mmol), [1,1′-bis(di-tert-butylphosphino)ferrocene]palladium(II) dichloride (30 mg, 10% wt) and the suspension was heated to 115° C. under microwave irradiation for 30 minutes. The resulting mixture was concentrated in vacuo and partitioned between DCM (50 mL) and water (50 mL). The organic phase was washed with brine (50 mL), dried (MgSO4), and evaporated in vacuo to give the title compound (200 mg, 77%) as a brown oil. LCMS (ES+) 212.0 (M+H)+, RT 1.78 minutes (70% purity) (Method 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242116B2
Source datasetuspto-grants-2012_08
ORD IDord-36642310d6664144b76b5f68ff44f51e
Source noteuspto-grants-2012_08