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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 2-Chloro-4-iodopyridine | HCID 1516511 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Dichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II) | HCID 53384307 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(2-Chloropyridin-4-YL)-4-methylpiperazine | HCID 72218899 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242116B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-36642310d6664144b76b5f68ff44f51e |
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| Source note | uspto-grants-2012_08 |
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