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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 885950Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/885950

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-MethylpiperazineHCID 53167—
Edukt2-Chloro-4-iodopyridineHCID 1516511—
EduktSodium t-butoxideHCID 23676156—
KatalysatorDichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II)HCID 53384307—
LösungsmittelTolueneHCID 1140—
Produkt1-(2-Chloropyridin-4-YL)-4-methylpiperazineHCID 7221889977%

Reaktionsbedingungen

Temperatur115 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08242116B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-36642310d6664144b76b5f68ff44f51e
Quellennotizuspto-grants-2012_08