Hexafluorophosphoric acid → 2-Bromo-5-(4-chloro-phenyl)-3-fluoro-pyridine

HRID 1916675Notes

Reaction equation

HRID 1916675 reaction equation
N([O-])=O.[Na+].[Br:5][C:6]1[C:11](N)=[CH:10][C:9]([C:13]2[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][CH:14]=2)=[CH:8][N:7]=1.[F:20][P-](F)(F)(F)(F)F.[H+]>O.Cl>[Br:5][C:6]1[C:11]([F:20])=[CH:10][C:9]([C:13]2[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][CH:14]=2)=[CH:8][N:7]=1

Participants

6

Conditions

Temperature
0 °C

Procedure

243 mg (3.53 mmol) sodium nitrite in 0.5 mL water are added dropwise at −5° C. to a solution of 1.00 g (3.53 mmol) 2-bromo-5-(4-chloro-phenyl)-pyridin-3-ylamine in 2 mL water and 2.04 mL concentrated HCl. Then at 0° C. 1.56 mL (10.6 mmol) 60% hexafluorophosphoric acid in water are added and the reaction is stirred for a further hour at 0° C. The diazonium salt is suction filtered, washed with cold water, isopropanol and ether and dried overnight in the desiccator at RT and 7 mbar. This is then added batchwise at 90° C. to 50 mL PE (boiling point 100-140° C.). After the reaction solution has cooled the mixture is made alkaline with saturated Na2CO3 solution. The aqueous phase is extracted with EtOAc and the organic phase is washed successively with saturated Na2CO3 solution and water. The organic phase is dried over MgSO4 and the solvent is eliminated i.vac.

Workup

  1. customat 0° C
  2. filtrationfiltered
  3. washwashed with cold water, isopropanol and ether
  4. customdried overnight in the desiccator at RT
  5. additionThis is then added batchwise at 90° C. to 50 mL PE (boiling point 100-140° C.)
  6. temperatureAfter the reaction solution has cooled the mixture
  7. extractionThe aqueous phase is extracted with EtOAc
  8. washthe organic phase is washed successively with saturated Na2CO3 solution and water
  9. dry with materialThe organic phase is dried over MgSO4

Sources & evidence

ORD record
ord-986aeb8cd33d4bc4b3af90c160850f9d
Source dataset
uspto-grants-2013_12
Patent number
US08618132B2

Reaction notes

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