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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Methylpiperazine | HCID 53167 | — |
| Edukt | 2-Chloro-4-iodopyridine | HCID 1516511 | — |
| Edukt | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | Dichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II) | HCID 53384307 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-(2-Chloropyridin-4-YL)-4-methylpiperazine | HCID 72218899 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08242116B2 |
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| Quelldatensatz | uspto-grants-2012_08 |
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| ORD ID | ord-36642310d6664144b76b5f68ff44f51e |
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| Quellennotiz | uspto-grants-2012_08 |
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