2,4-Dichloro-5-fluoropyrimidine → 2-Chloro-4-(1-ethoxyvinyl)-5-fluoropyrimidine

HRID 879636Notes

Reaction equation

HRID 879636 reaction equation
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([F:9])=[CH:4][N:3]=1.C([Sn](CCCC)(CCCC)[C:15]([O:17][CH2:18][CH3:19])=[CH2:16])CCC>CN(C=O)C>[Cl:1][C:2]1[N:7]=[C:6]([C:15]([O:17][CH2:18][CH3:19])=[CH2:16])[C:5]([F:9])=[CH:4][N:3]=1

Participants

4

Conditions

Temperature
75 °C

Procedure

To a solution of 2,4-dichloro-5-fluoro-pyrimidine (5.2 g, 31.14 mmol) in DMF (60 mL) was added tributyl-(1-ethoxy-vinyl)-stannane (12.37 g, 361.2 mmol), followed by dichlorobis(triphenylphosphine) palladium(II) (0.438 g, 0.623 mmol). The mixture was heated at 75° C. for 2 hours, cooled to rt and concentrated. The oily residue was dissolved in ethyl ether and a saturated solution of aqueous potassium fluoride was added and the mixture was stirred at room temperature for 18 hours. After dilution with EtOAc and filtration through Celite, the organic phase was washed with water, brine and concentrated. The crude material was purified by CombiFlash (0 to 10% EtOAc/Hex) to give desired product. LCMS-ESI+: calc'd for C8H9ClFN2O: 203.0 (M+H+); Found: 203.1 (M+H+); 1H NMR (400 MHz, Chloroform-d) δ 8.45 (d, J=2.8 Hz, 1H), 5.30 (d, J=3.1 Hz, 1H), 4.71 (d, J=3.1 Hz, 1H), 3.96 (q, J=7.0 Hz, 2H), 1.42 (t, J=7.0 Hz, 3H).

Workup

  1. temperaturecooled to rt
  2. concentrationconcentrated
  3. dissolutionThe oily residue was dissolved in ethyl ether
  4. additiona saturated solution of aqueous potassium fluoride was added
  5. filtrationAfter dilution with EtOAc and filtration through Celite
  6. washthe organic phase was washed with water, brine
  7. concentrationconcentrated
  8. customThe crude material was purified by CombiFlash (0 to 10% EtOAc/Hex)

Sources & evidence

ORD record
ord-1a620d7222644e5bbe3f983046e446c4
Source dataset
uspto-grants-2015_03
Patent number
US08987250B2

Reaction notes

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