Reaktionsgleichung
[C:1]([C:3]1[C:4]([Cl:14])=[N:5][C:6](Cl)=[CH:7][C:8]=1[C:9]([F:12])([F:11])[F:10])#[N:2].N[CH:16]([CH2:19]C)[CH2:17][OH:18].[CH:21]([NH:24]C(C)C)(C)C.ClCl>>[Cl:14][C:4]1[C:3]([C:1]#[N:2])=[C:8]([C:9]([F:12])([F:11])[F:10])[CH:7]=[C:6]([NH:24][CH2:21][CH:17]([OH:18])[CH2:16][CH3:19])[N:5]=1Komponenten
Versuchsvorschrift
Neat 3-cyano-2,6-dichloro-4-trifluoromethylpyridine (0.641 g, 6 mmol) was added by pipette at a dropwise rate over 3 minutes to 2-aminobutanol (1.5 g, 6 mmol). Di-isopropylamine (0.9 g, 7 mmol) was added after 10 minutes and the resultant mixture was heated in a sealed tube at 70° C. for 30 minutes to selectively displace the chlorine at position 6 before quenching in ice-cold water and extracted with dichloromethane. Organic extracts were washed twice with water, dried over sodium sulfate and concentrated under reduced pressure. The residue was washed with diethylether and the resultant solid was used in the next step without further purification. 2-Chloro-6-(2-hydroxybutylamino)-4-(trifluoromethyl) pyridine-3-carbonitrile was isolated in 55% yield.
Aufarbeitung
- custombefore quenching in ice-cold water
- extractionextracted with dichloromethane
- washOrganic extracts were washed twice with water
- dry with materialdried over sodium sulfate
- concentrationconcentrated under reduced pressure
- washThe residue was washed with diethylether
- customthe resultant solid was used in the next step without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-fad227854cef4529aa8948823934ee13
- Quelldatensatz
- uspto-grants-2013_12
- Patentnummer
- US08604199B2
Verknüpfte Notizen
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