Reaktionsgleichung
Br[C:2]1[C:3]([C:9]#[N:10])=[N:4][CH:5]=[C:6](C)[CH:7]=1.[C:11]([O-])([O-])=O.[K+].[K+].[N:17]1[NH:18][N:19]=[CH:20][CH:21]=1>CN(C=O)C>[CH3:11][C:5]1[N:4]=[C:3]([C:9]#[N:10])[C:2]([N:18]2[N:19]=[CH:20][CH:21]=[N:17]2)=[CH:7][CH:6]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
To 3-bromo-5-methylpicolinonitrile (2.2 g, 11 mmol) in DMF (28 mL) was added K2CO3 (1.7 g, 12 mmol) and 2H-1,2,3-triazole (650 μL, 11 mmol). The mixture was heated to 100° C. for 36 h, cooled to rt and extracted with EtOAc. The combined organics were dried (Na2SO4) and concentrated. Purification via silica gel chromatography (10-100% EtOAc in hexanes) gave the title compound (1 g, 48%).
Aufarbeitung
- temperaturecooled to rt
- extractionextracted with EtOAc
- dry with materialThe combined organics were dried (Na2SO4)
- concentrationconcentrated
- customPurification via silica gel chromatography (10-100% EtOAc in hexanes)
Quellen und Nachweise
- ORD-Eintrag
- ord-9f9d198fef8b4b5d9241029a89f23e2a
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09447117B2
Verknüpfte Notizen
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