Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Terbinafine | HCID 1549008 | — |
| Lösungsmittel | Methyl Ethyl Ketone | HCID 6569 | — |
| Produkt | Terbinafine Hydrochloride | HCID 5282481 | 75% |
Reaktionsschritte
169.9 g (0.420 mol theoretical) crude terbinafine (example 22) is dissolved in 306 ml methyl ethyl ketone (MEK) at 20/25° C.; then 41.3 ml (1 eq.) of 32% aqueous HCl are added dropwise at 20/30° C. Crystallisation of the product takes place during addition. The suspension is stirred for 15 minutes and then concentrated to a small volume under vacuum at 40° C. to azeotropically eliminate the water present, it is subsequently made up twice with MEK and again concentrated to a small volume under vacuum at 40° C. and finally diluted with MEK to restore it to the initial volume. The suspension is then cooled to −10° C. and stirred for 3 hours. The precipitate is filtered, washed with 2×69 ml cold MEK and dried to constant weight under vacuum at 40° C. 103.3 g (0.317 mol, 75% yield) terbinafine hydrochloride are obtained as a white crystalline solid with purity of 99.8% (HPLC A %) and a melting point of 207° C.-208° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07838704B2 |
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| Quelldatensatz | uspto-grants-2010_11 |
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| ORD ID | ord-ca70d0925c354b5e871fa203bad7a681 |
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| Quellennotiz | uspto-grants-2010_11 |
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