Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Piperazine | HCID 4837 | — |
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | 3,5-Dibromopyridine | HCID 69369 | — |
| Produkt | 1-(5-Bromopyridin-3-yl)-4-methylpiperazine | HCID 53485314 | — |
Reaktionsschritte
1-(5-Bromo-pyridin-3-yl)-4-methyl-piperazine was prepared from 3,5-dibromo-pyridine (1.00 g, 4.22 mmol) and piperazine, 1-methyl-(0.936 mL, 8.44 mmol) which were combined and heated in a microwave vial to 180° C. for 2 hours. The reaction mixture was taken up in dichloromethane and purified by silica gel chromatography 0-10% methanol in dichloromethane to afford a clear oil (37%). 1H NMR (400 MHz, (D3C)2SO, δ, ppm): 8.20 (s, 1H), 8.11 (s, 1H), 7.29 (m, 1H), 3.25 (bm, 4H), 2.58 (bm, 4H), 2.35 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08633173B2 |
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| Quelldatensatz | uspto-grants-2014_01 |
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| ORD ID | ord-6fe060a4e41f4a07abff5b18e0b3ca29 |
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| Quellennotiz | uspto-grants-2014_01 |
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