Methyl iodide → HCID 89648818, compound

HRID 1484688Notes

Reaction equation

HRID 1484688 reaction equation
[F:1][C:2]1[CH:19]=[CH:18][CH:17]=[CH:16][C:3]=1[CH2:4][N:5]1[C:9]([OH:10])=[CH:8][C:7]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[N:6]1.IC.[C:22](=O)([O-])[O-].[K+].[K+]>CC(C)=O>[F:1][C:2]1[CH:19]=[CH:18][CH:17]=[CH:16][C:3]=1[CH2:4][N:5]1[C:9]([O:10][CH3:22])=[CH:8][C:7]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[N:6]1

Participants

5

Procedure

21.58 g of ethyl 1-(2-fluorobenzyl)-5-hydroxy-1H-pyrazole-3-carboxylate 1-1-2 (81.66 mmol, 1.0 eq) were dissolved in dry acetone. Then 10.17 mL of iodomethane (163.3 mmol, 2.0 eq) and 40.63 g of potassium carbonate (294 mmol, 3.6 eq) were added. The precipitate was filtered off and the filtrate was concentrated in vacuo. The residue was partitioned between DCM and water, the aqueous layer was separated and extracted with DCM twice. The combined organic layers were dried over magnesium sulfate, filtered off and concentrated in vacuo to give 14.74 g (52.96 mmol, 65%) of the crude target compound that was used for the next transformation without further purification.

Workup

  1. filtrationThe precipitate was filtered off
  2. concentrationthe filtrate was concentrated in vacuo
  3. customThe residue was partitioned between DCM and water
  4. customthe aqueous layer was separated
  5. extractionextracted with DCM twice
  6. dry with materialThe combined organic layers were dried over magnesium sulfate
  7. filtrationfiltered off
  8. concentrationconcentrated in vacuo
  9. customto give 14.74 g (52.96 mmol, 65%) of the crude target compound that
  10. customwas used for the next transformation without further purification

Sources & evidence

ORD record
ord-bc5541b42a11467bb891f3d29d7d0e4e
Source dataset
uspto-grants-2016_08
Patent number
US09422268B2

Reaction notes

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