Trifluoroacetic acid → Trifluoroacetic acid
Reaktionsgleichung
[CH3:1][C@@H:2]([CH2:24][CH3:25])[C@H:3]([N:11]1[CH2:15][CH2:14][N:13]([CH2:16][C:17]2[N:18]=[C:19]([CH3:22])[S:20][CH:21]=2)[C:12]1=[O:23])[C:4]([O:6]C(C)(C)C)=[O:5].[F:26][C:27]([F:32])([F:31])[C:28]([OH:30])=[O:29]>ClCCl>[CH3:1][C@@H:2]([CH2:24][CH3:25])[C@H:3]([N:11]1[CH2:15][CH2:14][N:13]([CH2:16][C:17]2[N:18]=[C:19]([CH3:22])[S:20][CH:21]=2)[C:12]1=[O:23])[C:4]([OH:6])=[O:5].[F:26][C:27]([F:32])([F:31])[C:28]([OH:30])=[O:29]Komponenten
5
Edukt 2
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 25 °C
Versuchsvorschrift
A solution containing the product from Example 11C (2.0 g, 5.4 mmol) in dichloromethane (14 mL) was treated with trifluoracetic acid (7 mL), stirred at 25° C. for 3 hours and concentrated to give the title compound as a trifluoroacetic acid salt.
Aufarbeitung
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-59877b69e62e4bf19817fa5f1ab2e69d
- Quelldatensatz
- uspto-grants-2010_11
- Patentnummer
- US07834043B2
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