Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Tert-Butylamine | HCID 6385 | — |
| Edukt | Rosuvastatin n-butylamide | HCID 86699893 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | Rosuvastatin | HCID 446157 | 112,1% |
Reaktionsschritte
A 800 cm3 autoclave is charged with 16.1 g (0.03 mol) of rosuvastatin n-butylamide, 644 cm3 of water and 43.9 g (63.3 cm3; 0.60 mol) tert-butylamine. The reaction mixture is stirred for 24 hours at 120° C. The mixture is allowed to cool to room temperature, diluted with 2-propanol and evaporated in vacuo. The residue is stirred in the mixture of tert-butylmethylether and heptane (2:5, v/v) and the crystals are filtered. Thus 16.2 g (99%) of rosuvastatin TBA salt are obtained. The crude salt is boiled in acetonitrile/2-propanol (8.6:1, v/v) mixture, subsequently further stirred at room temperature, filtered, washed and dried. The product thus obtained is boiled in acetonitrile, 2-propanol is added to the boiling mixture, decolorized with carbon and filtered. The precipitated crystals are filtered and washed with acetonitrile. Yield 10.9 g (66%) rosuvastatin TBA salt having the purity (as determined by high-performance liquid chromatography, HPLC) exceeds 99.5%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09040696B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-374a57af9ef0443fb598448c797f88d6 |
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| Quellennotiz | uspto-grants-2015_05 |
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