Potassium Carbonate → 3-(4-Nitro-pyrazol-1-yl)-propan-1-ol

HRID 55871

Reaktionsgleichung

Reaktionsgleichung von HRID 55871
[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

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

  1. customThe solvent was evaporated in vacuo
  2. customthe residue partitioned between H2O (15 mL) and EtOAc (15 mL)
  3. customThe layers were separated
  4. extractionthe aqueous phase extracted with EtOAc (2×15 mL)
  5. dry with materialThe combined organics were dried (MgSO4)
  6. filtrationfiltered
  7. customthe solvent evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-5832e3deb7e74ffd9ceb999f45ff1987
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09433622B2

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