Phosphorus oxybromide → 4,7-Dibromofuro[3,2-c]pyridine

HRID 911944Notes

Reaction equation

HRID 911944 reaction equation
[Br:1][C:2]1[C:3]2[O:11][CH:10]=[CH:9][C:4]=2[C:5](=O)[NH:6][CH:7]=1.P(Br)(Br)([Br:14])=O>>[Br:14][C:5]1[C:4]2[CH:9]=[CH:10][O:11][C:3]=2[C:2]([Br:1])=[CH:7][N:6]=1

Participants

3

Conditions

Temperature
70 °C

Procedure

A mixture of 7-bromo-5H-furo[3,2-c]pyridin-4-one (21.2 g, 99 mmol) and POBr3 (31.2 g, 109 mmol) was heated at 70° C. for 5 min, then heated to 120° C. for 2 h. After cooled to rt, the solid was crashed and quenched with aqueous Na2CO3 (200 mL), then diluted with EtOAc (300 mL). The insoluble material was filtered off through a pad of Celite. The organic phase was collected and dried over Na2SO4. The crude material was purified by silica gel chromatography eluting with Hexanes-EtOAc (90:10→85:15) to give the title compound as a white solid (20.75 g, 68%). 1H NMR (CDCl3, 400 MHz): δ=6.91 (d, J=2.3 Hz, 1H), 7.79 (d, J=2.3 Hz, 1H), 8.37 (s, 1H).

Workup

  1. temperatureheated to 120° C. for 2 h
  2. temperatureAfter cooled to rt
  3. customquenched with aqueous Na2CO3 (200 mL)
  4. additiondiluted with EtOAc (300 mL)
  5. filtrationThe insoluble material was filtered off through a pad of Celite
  6. customThe organic phase was collected
  7. dry with materialdried over Na2SO4
  8. customThe crude material was purified by silica gel chromatography
  9. washeluting with Hexanes-EtOAc (90:10→85:15)

Sources & evidence

ORD record
ord-cc0b1653c1a24c6bb6f30b4490aa29cb
Source dataset
uspto-grants-2011_09
Patent number
US08022206B2

Reaction notes

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