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

HRID 1910867Notes

Reaction equation

HRID 1910867 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 (C-5) (400 mg, 2.94 mmol, 1.0 eq) is dissolved in POCl3 (10 mL, 109.2 mmol, 37.1 eq) and the resulting mixture is stirred at reflux for 2 h. The mixture is concentrated in vacuo to remove POCl3. The residue is 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 is extracted with ethyl acetate (30 mL×4). The combined organic layers are washed with brine, dried over Na2SO4 and filtered. The filtrate is concentrated in vacuo and the residue is purified by flash column chromatography on silica gel (16% ethyl acetate in petro ether) to afford the product, 4-chloroimidazo[1,2-f][1,2,4]triazine (C-6).

Workup

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

Sources & evidence

ORD record
ord-96603f235dfd4491a2be97c8c34e8c39
Source dataset
uspto-grants-2013_12
Patent number
US08604032B2

Reaction notes

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