Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Bromine | HCID 24408 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | HCID 178490904 | HCID 178490904 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 178490902 | HCID 178490902 | 87% |
Reaktionsschritte
Bromine (1.39 mL, 27.03 mmol) was added drop wise over 5 minutes to a solution of 1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-ol (6.00 g, 23.50 mmol, prepared as described in WO 2007/103308) in absolute ethanol (60 mL) at 0° C. The reaction was stirred at 0° C. for 1 hour. 5% Sodium bicarbonate solution (100 mL) was then added, and the mixture was concentrated to give a slurry. The pH was next adjusted with 1N HCl to a pH of 4. The resulting solid was collected by filtration and dried. This solid was then suspended in ether (50 mL), stirred for 10 minutes, collected by filtration and dried to give 5-bromo-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-ol (6.8 g, 87%). MS ESI (+) m/z 334 detected. 1H NMR (400 Hz, DMSO-d6) δ 12.68 (s, 1H), 8.34 (s, 1H), 8.13 (s, 1H), 7.18 (d, J=8.8 Hz, 2H), 6.87 (d, J=8.4 Hz, 2H), 5.47 (s, 2H), 3.70 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08372842B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-0645fd6a5fba40d3a9eb5cd81a0b88b3 |
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| Quellennotiz | uspto-grants-2013_02 |
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