Isopropyl iodide → 4-Iodo-1-(propan-2-yl)-1H-pyrazole

HRID 2246498Notes

Reaction equation

HRID 2246498 reaction equation
[H-].[Na+].[I:3][C:4]1[CH:5]=[N:6][NH:7][CH:8]=1.I[CH:10]([CH3:12])[CH3:11]>CN(C=O)C>[I:3][C:4]1[CH:5]=[N:6][N:7]([CH:10]([CH3:12])[CH3:11])[CH:8]=1

Participants

5

Procedure

To a slurry of sodium hydride (95%, 0.58 g, 23 mmol) in DMF (20 mL) was added a solution of 4-Iodo-1H-pyrazole (2023A) (4.07 g, 21 mmol) in DMF (20 mL) and the resulting mixture was stirred at rt for 10 min. Then 2-iodopropane (2.52 mL, 25.2 mmol) was added dropwise and the resulting mixture was stirred at rt overnight. The reaction mixture was concentrated, diluted with ethyl acetate, washed with water (4 times), brine, dried and concentrated to give an oily residue which was chromatographed (SiO2, 10%-20% ethyl acetate/hexane) to give 4-Iodo-1-isopropyl-1H-pyrazole 2023B (3.27 g, 66%). HPLC-MS tR=1.66 min (UV254 nm); mass calculated for formula C6H9IN2 235.98, observed LCMS m/z 237.0 (M+H).

Workup

  1. stirringthe resulting mixture was stirred at rt overnight
  2. concentrationThe reaction mixture was concentrated
  3. additiondiluted with ethyl acetate
  4. washwashed with water (4 times), brine
  5. customdried
  6. concentrationconcentrated
  7. customto give an oily residue which
  8. customwas chromatographed (SiO2, 10%-20% ethyl acetate/hexane)

Sources & evidence

ORD record
ord-53a252af5b084d17a15e4bc1e5195322
Source dataset
uspto-grants-2010_03
Patent number
US07687527B2

Reaction notes

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