Reaktionsgleichung
[CH3:1][C:2]1[C:3]([NH:9]C(C)(CC(C)(C)C)C)=[N:4][CH:5]=[C:6]([CH3:8])[CH:7]=1.FC(F)(F)C(O)=O>>[CH3:1][C:2]1[C:3]([NH2:9])=[N:4][CH:5]=[C:6]([CH3:8])[CH:7]=1Komponenten
3
Reaktionsbedingungen
- Temperatur
- 50 °C
Versuchsvorschrift
3,5-dimethyl-N-(2,4,4-trimethylpentan-2-yl)pyridin-2-amine (6.5 g, 27.7 mmol) was mixed with 2,2,2-trifluoroacetic acid (46 mL, 621 mmol) and heated to 50° C. for 4.5 hours. The mixture was concentrated in vacuo then diluted with dichloromethane (10 mL) and water (10 mL). The layers were partioned and aqueous phase was neutralised to pH 7-8 using saturated bicarbonate solution. The product was then extracted with dichloromethane (3×10 mL) and the organics were dried using a phase separator cartridge. The solvent was evaporated in vacuo to give the title compound (2.99 g) as a white solid. LCMS (2 min, High pH) Rt 0.69 min, m/z (ES+) 123 (M+H).
Aufarbeitung
- concentrationThe mixture was concentrated in vacuo
- additionthen diluted with dichloromethane (10 mL) and water (10 mL)
- extractionThe product was then extracted with dichloromethane (3×10 mL)
- customthe organics were dried
- customThe solvent was evaporated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-12402a79e13f45a6ba7c3ba17809153d
- Quelldatensatz
- uspto-grants-2016_01
- Patentnummer
- US09242972B2
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