Trifluoroacetic acid → Trifluoroacetic acid
Reaktionsgleichung
[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C@H:9]1[CH2:15][N:14]([CH2:16][C:17]([OH:20])([CH3:19])[CH3:18])[C:13](=[O:21])[C@H:12]([N:22](C(OC(C)(C)C)=O)C(OC(C)(C)C)=O)[CH2:11][CH2:10]1.[F:37][C:38]([F:43])([F:42])[C:39]([OH:41])=[O:40]>C(Cl)Cl>[NH2:22][C@@H:12]1[CH2:11][CH2:10][C@@H:9]([C:3]2[CH:4]=[CH:5][CH:6]=[C:7]([F:8])[C:2]=2[F:1])[CH2:15][N:14]([CH2:16][C:17]([OH:20])([CH3:18])[CH3:19])[C:13]1=[O:21].[C:39]([OH:41])([C:38]([F:43])([F:42])[F:37])=[O:40]Komponenten
5
Edukt 2
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of di-tert-butyl [(3R,6S)-6-(2,3-difluorophenyl)-1-(2-hydroxy-2-methylpropyl)-2-oxoazepan-3-yl]imidodicarbonate (0.095 g, 0.185 mmol) in DCM (10 mL) was treated with trifluoroacetic acid (3 mL). After 1 h the reaction was concentrated to dryness to afford the title compound as a TFA salt. MS 313.2 (M+1).
Aufarbeitung
- concentrationAfter 1 h the reaction was concentrated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-61fdd8d050f447e29fc17e133a444bf8
- Quelldatensatz
- uspto-grants-2008_11
- Patentnummer
- US07452903B2
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