1,3-Dichloroacetone → HCID 55267106, compound

HRID 422301Notes

Reaction equation

HRID 422301 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([NH2:8])=[N:6][CH:7]=1.[Cl:9][CH2:10][C:11](=O)[CH2:12]Cl>CCO>[Cl:9][CH2:10][C:11]1[N:8]=[C:5]2[CH:4]=[CH:3][C:2]([F:1])=[CH:7][N:6]2[CH:12]=1

Participants

4

Conditions

Temperature
80 °C

Procedure

According to the general protocol described in J. Heterocyclic. Chem., 1988, 25, 129-137, to solution of 5-fluoropyridin-2-amine (1.80 g, 16 mmol) in EtOH (24 mL) was added 1,3-dichloropropan-2-one (2.03 g, 16 mmol) and the resulting mixture was stirred overnight at 80° C. The solvent was evaporated, and the residue was dissolved in a minimum volume of water. The solution was neutralized (pH=8) with saturated NaHCO3. The aqueous layer was extracted with AcOEt and the organic layer was washed with saturated NaCl. The solvent was evaporated and The crude product was purified by chromatography (prepacked 25 g silicagel column, DCM as eluent) to afford 1.7 g of 2-(chloromethyl)-6-fluoro-imidazo[1,2-a]pyridine (Yield: 57%) as a beige solid.

Workup

  1. customThe solvent was evaporated
  2. dissolutionthe residue was dissolved in a minimum volume of water
  3. extractionThe aqueous layer was extracted with AcOEt
  4. washthe organic layer was washed with saturated NaCl
  5. customThe solvent was evaporated
  6. customThe crude product was purified by chromatography (prepacked 25 g silicagel column, DCM as eluent)

Sources & evidence

ORD record
ord-690a45c177a745c7aacb7183f3a0c928
Source dataset
uspto-grants-2012_01
Patent number
US08101637B2

Reaction notes

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