Phosphorus oxychloride → 4-Chloroimidazo(2,1-f)(1,2,4)triazine

HRID 869486Notes

Reaction equation

HRID 869486 reaction equation
[CH:1]1[N:5]=[C:4]2[C:6]([N:8]=[CH:9][NH:10][N:3]2[CH:2]=1)=O.O=P(Cl)(Cl)[Cl:13]>>[CH:1]1[N:5]=[C:4]2[C:6]([Cl:13])=[N:8][CH:9]=[N:10][N:3]2[CH:2]=1

Participants

3

Procedure

Imidazo[1,2-f][1,2,4]triazin-4-ol (400 mg, 2.94 mmol, 1.0 eq) was dissolved in POCl3 (10 mL, 109.2 mmol, 37.1 eq) and the resulting mixture was stirred at reflux for 2 h. The mixture was concentrated in vacuo to remove POCl3. The residue was poured into ice water (30 mL) and neutralized with saturated aqueous NaHCO3 solution to adjust the pH to 6-7 while keeping the temperature below 5° C. The mixture was extracted with ethyl acetate (30 mL×4). The combined organic layer was washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by flash column chromatography on silica gel (16% ethyl acetate in petro ether) to afford 4-chloroimidazo[1,2-f][1,2,4]triazine (300 mg, 66.0% yield).

Workup

  1. temperatureat reflux for 2 h
  2. concentrationThe mixture was concentrated in vacuo
  3. customto remove POCl3
  4. additionThe residue was poured into ice water (30 mL)
  5. customthe temperature below 5° C
  6. extractionThe mixture was extracted with ethyl acetate (30 mL×4)
  7. washThe combined organic layer was washed with brine
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. concentrationThe filtrate was concentrated in vacuo
  11. customthe residue was purified by flash column chromatography on silica gel (16% ethyl acetate in petro ether)

Sources & evidence

ORD record
ord-aab1362efc0e4500b087f6c156fbc655
Source dataset
uspto-grants-2015_03
Patent number
US08969363B2

Reaction notes

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