Reaktionsgleichung
[N+:1]([C:4]1[CH:5]=[N:6][NH:7][CH:8]=1)([O-:3])=[O:2].C([O-])([O-])=O.[K+].[K+].Br[CH2:16][CH2:17][CH2:18][OH:19]>CC#N>[N+:1]([C:4]1[CH:5]=[N:6][N:7]([CH2:16][CH2:17][CH2:18][OH:19])[CH:8]=1)([O-:3])=[O:2]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 75 °C
Versuchsvorschrift
To a stirred solution of 4-nitro-1H-pyrazole (27) (1.0 g, 8.9 mmol) in MeCN (15 mL) was added K2CO3 (1.8 g, 13.2 mmol) and 3-bromo-propanol (880 μL, 9.7 mmol). The mixture was stirred at 75° C. for 6 hours. The solvent was evaporated in vacuo and the residue partitioned between H2O (15 mL) and EtOAc (15 mL). The layers were separated and the aqueous phase extracted with EtOAc (2×15 mL). The combined organics were dried (MgSO4), filtered and the solvent evaporated in vacuo to afford the title compound as a pale yellow oil (1.41 g, 93%); LCMS, Rt=1.31 min (MeOH-FA method), m/z 172 (MH+).
Aufarbeitung
- customThe solvent was evaporated in vacuo
- customthe residue partitioned between H2O (15 mL) and EtOAc (15 mL)
- customThe layers were separated
- extractionthe aqueous phase extracted with EtOAc (2×15 mL)
- dry with materialThe combined organics were dried (MgSO4)
- filtrationfiltered
- customthe solvent evaporated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-5832e3deb7e74ffd9ceb999f45ff1987
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09433622B2
Verknüpfte Notizen
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