HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40703Erstellt: 26. Oktober 2026
5-Bromo-2-fluoropyridine → 1-Tert-butyl-4-(6-fluoropyridin-3-yl)piperazine
https://huagongshe.com/reaction/40703
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 5-Bromo-2-fluoropyridine | HCID 2783168 | — |
| Edukt | 1-Tert-butylpiperazine | HCID 3530572 | — |
| Edukt | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Edukt | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-Tert-butyl-4-(6-fluoropyridin-3-yl)piperazine | HCID 67412191 | 71% |
Reaktionsschritte
1-tert-Butylpiperazine (1.61 g, 11.4 mmol) is placed in 35 ml of toluene under nitrogen, 5-Bromo-2-fluoropyridine (2 g, 11.4 mmol), sodium t-butoxide (1.6 g, 17 mmol), tris(dibenzylideneacetone)dipalladium (0.52 g, 0.57 mmol), and S-Phos (0.93 g, 17 mmol) are then added. The reaction medium is heated at 80° C. for 18 h. After hydrolysis, and extraction with ethyl acetate, the organic phase is washed with water and then with a saturated aqueous sodium chloride solution. After drying over MgSO4, and concentrating to dryness, the crude product obtained is chromatographed on silica gel, elution being carried out with a gradient of methanol in dichloromethane ranging from 0% to 5%. 1.92 g of 1-tert-butyl-4-(6-fluoropyridin-3-yl)piperazine are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08530477B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-1415b2b69aab4cb587315c27bb5ff3fe |
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| Quellennotiz | uspto-grants-2013_09 |
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