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

HRID 55871

Reaction equation

HRID 55871 reaction equation
[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]

Participants

5

Conditions

Temperature
75 °C

Procedure

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+).

Workup

  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

Sources & evidence

ORD record
ord-5832e3deb7e74ffd9ceb999f45ff1987
Source dataset
uspto-grants-2016_09
Patent number
US09433622B2

Linked notes

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