Trifluoroacetic acid → 6-Bromo-1,2,3,4-tetrahydro-3-quinolinamine
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH2:7][CH:6]([NH:12]C(=O)OC(C)(C)C)[CH2:5]2.FC(F)(F)C(O)=O>ClCCl>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH2:7][CH:6]([NH2:12])[CH2:5]2Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of (6-Bromo-1,2,3,4-tetrahydro-3-quinolinyl)carbamic acid, 1,1-dimethylethyl ester (652 mg, 2 mmol) in dichloromethane at RT under argon was added trifluoroacetic acid (1 mL). After 3 hours, the mixture was concentrated. Chloroform (10 mL) was added and concentrated again in vacuo to afford the title compound (1 g), an oil, which was used without further purification. MS; M(+H)+=227.
Aufarbeitung
- concentrationthe mixture was concentrated
- additionChloroform (10 mL) was added
- concentrationconcentrated again in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-22b7c889761f4e31b5c5e5a92dd0735a
- Quelldatensatz
- uspto-grants-2002_05
- Patentnummer
- US06387926B1
Notizen zur Reaktion
Wird geladen…