Sodium Carbonate → 6-Bromo-3-fluoroisoquinoline

HRID 2075389Notes

Reaction equation

HRID 2075389 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[N:7][C:6](N)=[CH:5]2.[FH:13].N1C=CC=CC=1.N([O-])=O.[Na+].C([O-])([O-])=O.[Na+].[Na+]>>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[N:7][C:6]([F:13])=[CH:5]2

Participants

5

Conditions

Temperature
-78 °C

Procedure

To a mixture of 6-bromoisoquinolin-3-amine (0.710 g, 3.18 mmol) in pyridine hydrofluoride (10 mL, 3.18 mmol) at −78° C. was carefully added sodium nitrite (0.26 g, 3.82 mmol). The reaction mixture was stirred at −78° C. for 5 minutes. The reaction mixture was warmed to room temperature over 40 minutes. The mixture was poured into an ice bath, and the pH was adjusted to >9 with Na2CO3. The mixture was filtered to recover a yellow-purple solid. The solid was dissolved in EtOAc-water with stirring. The mixture was extracted with EtOAc (3×200 mL). The EtOAc was washed with brine, dried over Na2SO4, filtered and concentrated. The residue was taken up in DCM-MeOH and adsorbed onto silica gel. Purification by chromatography on silica gel (EtOAc 0-7% in hexane) provided the product (500 mg, 70%). LCMS (API-ES) m/z: 226, 228 (M+H+).

Workup

  1. temperatureThe reaction mixture was warmed to room temperature over 40 minutes
  2. additionThe mixture was poured into an ice bath
  3. filtrationThe mixture was filtered
  4. customto recover a yellow-purple solid
  5. dissolutionThe solid was dissolved in EtOAc-water
  6. stirringwith stirring
  7. extractionThe mixture was extracted with EtOAc (3×200 mL)
  8. washThe EtOAc was washed with brine
  9. dry with materialdried over Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated
  12. customPurification by chromatography on silica gel (EtOAc 0-7% in hexane)

Sources & evidence

ORD record
ord-88e1b175bf58435aaadcddfcee80f7e2
Source dataset
uspto-grants-2011_04
Patent number
US07919504B2

Reaction notes

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