Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 2,6-Dibromopyridine | HCID 12274 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 4-(Pyrrolidin-1-ylmethyl)phenol | HCID 18771978 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-Bromo-6-[4-(1-pyrrolidinylmethyl)phenoxy]pyridine | HCID 18771652 | — |
Reaktionsschritte
To a stirred suspension of NaH (2.6 g, 108.5 mmol) in DMF (300 mL) at 0° C., under N2, a solution of 4-pyrrolidin-1-ylmethylphenol (16 g, 90.4 mmol) was added slowly. After stirring at 0° C. for 30 min, 2,6-dibromopyridine (23.6 g, 99.4 mmol) was added and the resulting mixture was heated at 95° C. for 20 h. After cooling to RT, 200 mL of H2O was added and the mixture was extracted with EtOAc (3×300 mL). The combined organic layer was washed with brine (3×400 mL), dried over MgSO4, filtered and concentrated under reduced pressure to yield the title compound as an amber solid. This was used crude in the next step. MS m/z: 333 (M+1). Calc'd for C16H17BrN2O-333.2
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07196104B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-cefd933575fd4c18a2f7015429234586 |
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| Quellennotiz | uspto-grants-2007_03 |
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