Bromide ion → 2-(6-bromo-1H-pyrrolo[2,3-b]pyridin-1-yl)(phenyl)methanone

HRID 253469Notes

Reaction equation

HRID 253469 reaction equation
[NH+:1]1([O-])[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[CH:2]1.[C:11](Br)(=[O:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C[Si](C)(C)N[Si](C)(C)C.[Br-:29]>C1C=CC=CC=1>[Br:29][C:7]1[N:6]=[C:5]2[N:1]([C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=3[CH:11]=[O:18])[CH:2]=[CH:3][C:4]2=[CH:9][CH:8]=1

Participants

6

Reactant 4

HCID 259Bromide ionHCID 12056Benzoyl bromideHCID 13838HexamethyldisilazaneHCID 219590977-aza-1H-indole N-oxide

Product 1

HCID 866231352-(6-bromo-1H-pyrrolo[2,3-b]pyridin-1-yl)(phenyl)methanone

Reagents, catalysts & solvents 1

HCID 241BenzeneSolvent2×

Procedure

1H-pyrrolo[2,3-b]pyridine-N-oxide (154, 500 mg, 3.72 mmol) was dissolved in 40 mL of dry benzene. In a separate dry flask, benzoyl bromide (2.5 equiv) and 1,1,1,3,3,3-hexamethyldisilazane (1.0 equiv) were combined in 20 mL of dry benzene. The bromide solution was added in 5 mL aliquots over 30 minutes to the reaction flask. The reaction was stirred at ambient temperature for two hours. It was then washed with 3×30 ml, NaHCO3 (aq., satd.) and 1×30 mL brine. The organic layer was dried over sodium sulfate and evaporated. The crude material was taken directly to the next step without further purification.

Workup

  1. customIn a separate dry flask
  2. washIt was then washed with 3×30 ml, NaHCO3 (aq., satd.) and 1×30 mL brine
  3. dry with materialThe organic layer was dried over sodium sulfate
  4. customevaporated
  5. customThe crude material was taken directly to the next step without further purification

Sources & evidence

ORD record
ord-8c0515b7fc5e4843b1d1600370e8882d
Source dataset
uspto-grants-2011_01
Patent number
US07872018B2

Reaction notes

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