Reaktionsgleichung
[N+:1]([CH2:4][CH:5]([NH:16]C(=O)OC(C)(C)C)[C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([C:12]([F:15])([F:14])[F:13])[CH:7]=1)([O-:3])=[O:2].[ClH:24]>O1CCOCC1>[ClH:24].[N+:1]([CH2:4][CH:5]([C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([C:12]([F:13])([F:14])[F:15])[CH:7]=1)[NH2:16])([O-:3])=[O:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Of the compound from Example 12A, 340 mg (1.02 mmol) were admixed at RT with 6.8 ml of a 4N solution of hydrogen chloride in dioxane, and stirred for 1 h. The reaction mixture was concentrated under reduced pressure and dried in an HV. This gave 274 mg (99% of theory) of the title compound.
Aufarbeitung
- concentrationThe reaction mixture was concentrated under reduced pressure
- customdried in an HV
Quellen und Nachweise
- ORD-Eintrag
- ord-9f140f45327940efaf8114ff642eb124
- Quelldatensatz
- uspto-grants-2012_06
- Patentnummer
- US08202895B2
Verknüpfte Notizen
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