Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrogen Bromide | HCID 260 | — |
| Edukt | Noscapine | HCID 275196 | — |
| Edukt | HCID 178514845 | HCID 178514845 | — |
| Produkt | 9-Bromonoscapine | HCID 10255081 | 82% |
Reaktionsschritte
Targetin was synthesized using a four-step synthetic scheme, as illustrated below. Noscapine (1) was brominated by adding 48% hydrobromic acid and freshly prepared bromine water. The reaction mixture was stirred for 1 hr at 25° C., and basified to pH 10 to yield 9-bromonoscapine (2) in ˜82% yield. Refluxing compound 2 in dimethyl formamide with sodium azide and sodium iodide for 15 hrs gave the corresponding azido derivative (3), which when reduced with tin chloride in the presence of thiophenol and triethylamine in tetrahydrofuran for 2 hrs at 25° C. to provide 9-aminonoscapine (4) in ˜83% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08426398B2 |
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| Quelldatensatz | uspto-grants-2013_04 |
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| ORD ID | ord-889d2a73c91f4c0191ea369640bb008f |
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| Quellennotiz | uspto-grants-2013_04 |
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