Water → 3-iodo-1-methyl-6-(trifluoromethyl)-1H-indazole

HRID 246658Notes

Reaction equation

HRID 246658 reaction equation
[I:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([F:14])([F:13])[F:12])=[CH:8][CH:9]=2)[NH:4][N:3]=1.[CH3:15]C([O-])(C)C.[K+].IC.O>O1CCCC1>[I:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([F:13])([F:12])[F:14])=[CH:8][CH:9]=2)[N:4]([CH3:15])[N:3]=1

Participants

6

Procedure

To a solution of 3-iodo-6-(trifluoromethyl)-1H-indazole (650 mg, 2.09 mmol) in dry tetrahydrofuran (20 mL) was added potassium 2-methylpropan-2-olate (0.35 mL, 3.13 mmol) at 0° C. under N2 atmosphere. After 30 minutes, iodomethane (445 mg, 3.13 mmol) was added dropwise at 0° C., then it was warmed to room temperature for 2 h. Water (2 mL) was added and product extracted with dichloromethane (150 mL), then organic phase washed with water (2×20 mL), brine (2×20 mL) then dried over Na2SO4, filtered and concentrated. The residue was washed with petroleum ether (2 mL) and filtered to afford 3-iodo-1-methyl-6-(trifluoromethyl)-1H-indazole (491 mg, 72%) as a white solid. LCMS: (M+H)+=327.

Workup

  1. extractionproduct extracted with dichloromethane (150 mL)
  2. washorganic phase washed with water (2×20 mL), brine (2×20 mL)
  3. dry with materialthen dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. washThe residue was washed with petroleum ether (2 mL)
  7. filtrationfiltered

Sources & evidence

ORD record
ord-ea8dc343328848c5a77e7552bf8ff9d2
Source dataset
uspto-grants-2014_02
Patent number
US08658646B2

Reaction notes

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