Water → Methyl 5-fluoro-6-oxo-1,6-dihydropyridine-3-carboxylate

HRID 2370823Notes

Reaction equation

HRID 2370823 reaction equation
[O:1]=[C:2]1[NH:7][CH:6]=[C:5]([C:8]([O:10][CH3:11])=[O:9])[CH:4]=[CH:3]1.[B-](F)(F)(F)[F:13].[B-](F)(F)(F)F.C1[N+]2(CCl)CC[N+](F)(CC2)C1.O>CC#N>[F:13][C:3]1[C:2](=[O:1])[NH:7][CH:6]=[C:5]([C:8]([O:10][CH3:11])=[O:9])[CH:4]=1

Participants

5

Conditions

Temperature
65 °C

Procedure

To a solution of methyl 6-oxo-1,6-dihydro-3-pyridinecarboxylate (2.00 g, 13.06 mmol, Bionet Research) in MeCN (40 mL) was added SelectFluor® (4.63 g, 13.06 mmol, Aldrich). The resulting mixture was then heated at 65° C. for 18 h. Then, the mixture was cooled to rt and water (20 mL) was added. The solvent, (MeCN) was removed and the remaining aqueous solution was extracted with EtOAc (2×20 mL). The combined organic extracts were dried (MgSO4) and concentrated in vacuo. The residue was dissolved in MeOH (100 mL) and silica gel was added. The mixture was concentrated and dried in vacuo. Purification by silica gel flash column chromatography (0%-100% EtOAc/hexane) gave the title compound as a white solid. MS (ESI, positive ion) m/z: 172 (M+H).

Workup

  1. temperatureThen, the mixture was cooled to rt
  2. customThe solvent, (MeCN) was removed
  3. extractionthe remaining aqueous solution was extracted with EtOAc (2×20 mL)
  4. dry with materialThe combined organic extracts were dried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. dissolutionThe residue was dissolved in MeOH (100 mL)
  7. additionsilica gel was added
  8. concentrationThe mixture was concentrated
  9. customdried in vacuo
  10. customPurification by silica gel flash column chromatography (0%-100% EtOAc/hexane)

Sources & evidence

ORD record
ord-4ae84ccc3ba34794b4f5a994c0c4fb98
Source dataset
uspto-grants-2014_04
Patent number
US08710043B2

Reaction notes

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