Potassium Phosphate, Tribasic → 4-iodo-2H,3H-furo(2,3-b)pyridine

HRID 924413Notes

Reaction equation

HRID 924413 reaction equation
F[C:2]1[C:7]([CH2:8][CH2:9][OH:10])=[C:6]([I:11])[CH:5]=[CH:4][N:3]=1.[O-]P([O-])([O-])=O.[K+].[K+].[K+]>O1CCOCC1>[I:11][C:6]1[CH:5]=[CH:4][N:3]=[C:2]2[O:10][CH2:9][CH2:8][C:7]=12

Participants

4

Procedure

To a solution of 2-(2-fluoro-4-iodopyridin-3-yl)ethanol (3.13 g, 11.7 mmol) in 1,4-dioxane (100 mL), K3PO4 (10.0 g, 47.1 mmol) was added. The mixture was heated under reflux for 36 h. The reaction mixture was then filtered, the filter cake was washed with EtOAc, and the combined filtrates were concentrated under reduced pressure. The residue was dissolved in DCM (100 mL), washed with brine (2×100 mL), dried over Na2SO4 and concentrated. The resulting residue of the crude sub-title compound (2.55 g) was used in the next step directly without further purification. LCMS calc. for C7H7INO (M+H)+: m/z=247.9. found 248.0.

Workup

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 36 h
  3. filtrationThe reaction mixture was then filtered
  4. washthe filter cake was washed with EtOAc
  5. concentrationthe combined filtrates were concentrated under reduced pressure
  6. dissolutionThe residue was dissolved in DCM (100 mL)
  7. washwashed with brine (2×100 mL)
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated
  10. customThe resulting residue of the crude sub-title compound (2.55 g) was used in the next step directly without further purification

Sources & evidence

ORD record
ord-b7c6b682849e46b8816d5a1546c364a6
Source dataset
uspto-grants-2016_03
Patent number
US09278950B2

Reaction notes

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